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		<id>http://192.168.164.12:81/ricewiki/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Liye</id>
		<title>RiceWiki - User contributions [en]</title>
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		<updated>2026-05-24T16:18:47Z</updated>
		<subtitle>User contributions</subtitle>
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	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=BPH_gene&amp;diff=183826</id>
		<title>BPH gene</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=BPH_gene&amp;diff=183826"/>
				<updated>2014-06-11T03:14:11Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* Mapping of BPH gene */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;    The brown planthopper (BPH), Nilaparvata lugens, is one of the most serious insect pests throughout rice growing areas in Asia. This is especially true in countries mainly culturing Japonica rice cultivars that do not have a gene conferring resistance to BPH, and where outbreaks of BHP are therefore a severe problem. The BPH causes direct damage to crops and indirect damage by acting as a vector for viral diseases. Chemical treatment is the conventional method of controlling pests such as BPH, even though it is expensive and harmful to the environment. Many researchers have reported that host plant resistance is the most effective way of controlling pests including BPH, and thus breeding of insect resistance has taken priority in rice improvement programs. Until now, 13BPH resistance genes, together with several quantitative trait loci (QTLs) controlling BPH resistance, have been reported in two wild relatives and indica cultivars. Diverse sources of BPH resistance have been identified and genetic analysis has revealed 6 dominant [Bph1, 3, 6, 9, 10, and 13(t)] and 7 recessive [bph2, 4, 5, 7, 8, 11(t), and 12(t)] genes controlling BPH resistance. Bph1, bph2, Bph9, and Bph10(t) were assigned to rice chromosome 12. Bph1 and bph2 confer resistance to biotypes 1, 3 and 1, 2 which are widely distributed in Southeast Asia. Many studies aimed at identifying BPH resistance genes have been conducted over the years in order to develop a resistant cultivar; however, a japonica cultivar with a BPH resistance gene has not yet been developed. Thirteen of the BPH resistance genes identified so far are not from japonica rice, but from indica rice. In bioassays, it has been reported that the reaction of early rice seedlings to BPH differed between japonica and indica. Japonica introgression lines with BPH resistance genes exhibited undesirable characteristics such as poor grain quality and lodging-related traits to which the resistance genes seemed to be highly linked. The undesirable linkage drag between a BPH resistance gene and genes conferring agriculturally important characters may be removed by intensive work to select recombinants between the traits, and a molecular marker tightly linked to the target gene could be useful for selecting the desired recombinants。&lt;br /&gt;
    The use of tightly linked genetic markers for resistance genes offers great scope for improving the efficiency of conventional plant breeding by allowing selection to be based on molecular markers linked to a trait at an early stage of growth, rather than being based on the trait itself. Resistance genes to gall midge and blast have been identified in rice, and linkage between DNA markers and these resistance genes has been analyzed. In this way linkage maps of genes associated with resistance to diseases and pests have been constructed in wheat, barley, and other economically important crops. The current study was conducted to identify Bph1-related DNA markers in rice, and thus to permit the establishment of a marker-assisted breeding program to introgress the BPH-resistance gene into japonica rice cultivars.&lt;br /&gt;
&lt;br /&gt;
== BPH Evalution ==&lt;br /&gt;
Brown planthopper (Nilaparvata lugens Stål.) is one of the most damaging pests of rice in Asia. It causes severe yield reduction by directly sucking the plant sap and acting as a vector of virus diseases such as rice grassy stunt and ragged stunt (Khush and Brar, 1991). Host plant resistance has been recognized as significant strategy to control BPH damage in contrast to the chemical control. The genetics of BPH resistance is well studied and as many as 21 major genes have been identified in cultivated and wild species (Qifa Zhang, 2007 and Fujita et al., 2008). Among the BPH biotypes prevailing in South East Asia, biotype 4 is the most destructive and distributed over the Indian subcontinent (Heinrichs, 1986). The biotype variations results in overcome of resistance to several major genes, therefore, the identification of additional BPH resistance genes is required to address the issue of durable resistance.&lt;br /&gt;
== Mapping of BPH gene ==&lt;br /&gt;
The repeated screening over the years of different donors with known gene, against local BPH biotype available at the Directorate of Rice Research, Hyderabad, India, recorded consistent resistance in Rathu Henati (Bph3 &amp;amp; Bph17), Swarnalatha (Bph 6) and ADR 52 (bph20(t) &amp;amp; Bph21(t)). While rest of other donors Mudgo (Bph1), IR 56 (Bph3), Pokkali (Bph9), IR 65482-4-136-2-2 (Bph10), IR 65482-7-216-1-2 (Bph18) showed either susceptible or moderate resistance(Table 1&amp;amp;Table 2).&lt;br /&gt;
&lt;br /&gt;
[[File:Table 1.PNG]]&lt;br /&gt;
[[File:Table 2.PNG]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Reference ==&lt;br /&gt;
1. T. RAM;R. DEEN;S. K. GAUTAM;K. RAMESH;Y. K. RAO;D. S. BRAR,  Identification of new genes for Brown Planthopper resistance in rice introgressed from O. glaberrima and O. minuta. Rice Genetics Newsletters, 2010, 25(): 67-69&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=BPH_gene&amp;diff=183825</id>
		<title>BPH gene</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=BPH_gene&amp;diff=183825"/>
				<updated>2014-06-11T03:12:14Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* Mapping of BPH gene */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;    The brown planthopper (BPH), Nilaparvata lugens, is one of the most serious insect pests throughout rice growing areas in Asia. This is especially true in countries mainly culturing Japonica rice cultivars that do not have a gene conferring resistance to BPH, and where outbreaks of BHP are therefore a severe problem. The BPH causes direct damage to crops and indirect damage by acting as a vector for viral diseases. Chemical treatment is the conventional method of controlling pests such as BPH, even though it is expensive and harmful to the environment. Many researchers have reported that host plant resistance is the most effective way of controlling pests including BPH, and thus breeding of insect resistance has taken priority in rice improvement programs. Until now, 13BPH resistance genes, together with several quantitative trait loci (QTLs) controlling BPH resistance, have been reported in two wild relatives and indica cultivars. Diverse sources of BPH resistance have been identified and genetic analysis has revealed 6 dominant [Bph1, 3, 6, 9, 10, and 13(t)] and 7 recessive [bph2, 4, 5, 7, 8, 11(t), and 12(t)] genes controlling BPH resistance. Bph1, bph2, Bph9, and Bph10(t) were assigned to rice chromosome 12. Bph1 and bph2 confer resistance to biotypes 1, 3 and 1, 2 which are widely distributed in Southeast Asia. Many studies aimed at identifying BPH resistance genes have been conducted over the years in order to develop a resistant cultivar; however, a japonica cultivar with a BPH resistance gene has not yet been developed. Thirteen of the BPH resistance genes identified so far are not from japonica rice, but from indica rice. In bioassays, it has been reported that the reaction of early rice seedlings to BPH differed between japonica and indica. Japonica introgression lines with BPH resistance genes exhibited undesirable characteristics such as poor grain quality and lodging-related traits to which the resistance genes seemed to be highly linked. The undesirable linkage drag between a BPH resistance gene and genes conferring agriculturally important characters may be removed by intensive work to select recombinants between the traits, and a molecular marker tightly linked to the target gene could be useful for selecting the desired recombinants。&lt;br /&gt;
    The use of tightly linked genetic markers for resistance genes offers great scope for improving the efficiency of conventional plant breeding by allowing selection to be based on molecular markers linked to a trait at an early stage of growth, rather than being based on the trait itself. Resistance genes to gall midge and blast have been identified in rice, and linkage between DNA markers and these resistance genes has been analyzed. In this way linkage maps of genes associated with resistance to diseases and pests have been constructed in wheat, barley, and other economically important crops. The current study was conducted to identify Bph1-related DNA markers in rice, and thus to permit the establishment of a marker-assisted breeding program to introgress the BPH-resistance gene into japonica rice cultivars.&lt;br /&gt;
&lt;br /&gt;
== BPH Evalution ==&lt;br /&gt;
Brown planthopper (Nilaparvata lugens Stål.) is one of the most damaging pests of rice in Asia. It causes severe yield reduction by directly sucking the plant sap and acting as a vector of virus diseases such as rice grassy stunt and ragged stunt (Khush and Brar, 1991). Host plant resistance has been recognized as significant strategy to control BPH damage in contrast to the chemical control. The genetics of BPH resistance is well studied and as many as 21 major genes have been identified in cultivated and wild species (Qifa Zhang, 2007 and Fujita et al., 2008). Among the BPH biotypes prevailing in South East Asia, biotype 4 is the most destructive and distributed over the Indian subcontinent (Heinrichs, 1986). The biotype variations results in overcome of resistance to several major genes, therefore, the identification of additional BPH resistance genes is required to address the issue of durable resistance.&lt;br /&gt;
== Mapping of BPH gene ==&lt;br /&gt;
The repeated screening over the years of different donors with known gene, against local BPH biotype available at the Directorate of Rice Research, Hyderabad, India, recorded consistent resistance in Rathu Henati (Bph3 &amp;amp; Bph17), Swarnalatha (Bph 6) and ADR 52 (bph20(t) &amp;amp; Bph21(t)). While rest of other donors Mudgo (Bph1), IR 56 (Bph3), Pokkali (Bph9), IR 65482-4-136-2-2 (Bph10), IR 65482-7-216-1-2 (Bph18) showed either susceptible or moderate resistance(Table 1&amp;amp;Table 2).&lt;br /&gt;
&lt;br /&gt;
[[File:Table 1.PNG]]&lt;br /&gt;
[[File:Table 2.PNG]]&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=BPH_gene&amp;diff=183824</id>
		<title>BPH gene</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=BPH_gene&amp;diff=183824"/>
				<updated>2014-06-11T03:11:43Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* Mapping of BPH gene */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;    The brown planthopper (BPH), Nilaparvata lugens, is one of the most serious insect pests throughout rice growing areas in Asia. This is especially true in countries mainly culturing Japonica rice cultivars that do not have a gene conferring resistance to BPH, and where outbreaks of BHP are therefore a severe problem. The BPH causes direct damage to crops and indirect damage by acting as a vector for viral diseases. Chemical treatment is the conventional method of controlling pests such as BPH, even though it is expensive and harmful to the environment. Many researchers have reported that host plant resistance is the most effective way of controlling pests including BPH, and thus breeding of insect resistance has taken priority in rice improvement programs. Until now, 13BPH resistance genes, together with several quantitative trait loci (QTLs) controlling BPH resistance, have been reported in two wild relatives and indica cultivars. Diverse sources of BPH resistance have been identified and genetic analysis has revealed 6 dominant [Bph1, 3, 6, 9, 10, and 13(t)] and 7 recessive [bph2, 4, 5, 7, 8, 11(t), and 12(t)] genes controlling BPH resistance. Bph1, bph2, Bph9, and Bph10(t) were assigned to rice chromosome 12. Bph1 and bph2 confer resistance to biotypes 1, 3 and 1, 2 which are widely distributed in Southeast Asia. Many studies aimed at identifying BPH resistance genes have been conducted over the years in order to develop a resistant cultivar; however, a japonica cultivar with a BPH resistance gene has not yet been developed. Thirteen of the BPH resistance genes identified so far are not from japonica rice, but from indica rice. In bioassays, it has been reported that the reaction of early rice seedlings to BPH differed between japonica and indica. Japonica introgression lines with BPH resistance genes exhibited undesirable characteristics such as poor grain quality and lodging-related traits to which the resistance genes seemed to be highly linked. The undesirable linkage drag between a BPH resistance gene and genes conferring agriculturally important characters may be removed by intensive work to select recombinants between the traits, and a molecular marker tightly linked to the target gene could be useful for selecting the desired recombinants。&lt;br /&gt;
    The use of tightly linked genetic markers for resistance genes offers great scope for improving the efficiency of conventional plant breeding by allowing selection to be based on molecular markers linked to a trait at an early stage of growth, rather than being based on the trait itself. Resistance genes to gall midge and blast have been identified in rice, and linkage between DNA markers and these resistance genes has been analyzed. In this way linkage maps of genes associated with resistance to diseases and pests have been constructed in wheat, barley, and other economically important crops. The current study was conducted to identify Bph1-related DNA markers in rice, and thus to permit the establishment of a marker-assisted breeding program to introgress the BPH-resistance gene into japonica rice cultivars.&lt;br /&gt;
&lt;br /&gt;
== BPH Evalution ==&lt;br /&gt;
Brown planthopper (Nilaparvata lugens Stål.) is one of the most damaging pests of rice in Asia. It causes severe yield reduction by directly sucking the plant sap and acting as a vector of virus diseases such as rice grassy stunt and ragged stunt (Khush and Brar, 1991). Host plant resistance has been recognized as significant strategy to control BPH damage in contrast to the chemical control. The genetics of BPH resistance is well studied and as many as 21 major genes have been identified in cultivated and wild species (Qifa Zhang, 2007 and Fujita et al., 2008). Among the BPH biotypes prevailing in South East Asia, biotype 4 is the most destructive and distributed over the Indian subcontinent (Heinrichs, 1986). The biotype variations results in overcome of resistance to several major genes, therefore, the identification of additional BPH resistance genes is required to address the issue of durable resistance.&lt;br /&gt;
== Mapping of BPH gene ==&lt;br /&gt;
&lt;br /&gt;
 The repeated screening over the years of different donors with known gene, against local BPH biotype available at the Directorate of Rice Research, Hyderabad, India, recorded consistent resistance in Rathu Henati (Bph3 &amp;amp; Bph17), Swarnalatha (Bph 6) and ADR 52 (bph20(t) &amp;amp; Bph21(t)). While rest of other donors Mudgo (Bph1), IR 56 (Bph3), Pokkali (Bph9), IR 65482-4-136-2-2 (Bph10), IR 65482-7-216-1-2 (Bph18) showed either susceptible or moderate resistance(Table 1&amp;amp;Table 2).&lt;br /&gt;
[[File:Table 1.PNG]]&lt;br /&gt;
[[File:Table 2.PNG]]&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:Table_2.PNG&amp;diff=183822</id>
		<title>File:Table 2.PNG</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:Table_2.PNG&amp;diff=183822"/>
				<updated>2014-06-11T03:11:25Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=BPH_gene&amp;diff=183821</id>
		<title>BPH gene</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=BPH_gene&amp;diff=183821"/>
				<updated>2014-06-11T03:11:06Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* Mapping of BPH gene */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;    The brown planthopper (BPH), Nilaparvata lugens, is one of the most serious insect pests throughout rice growing areas in Asia. This is especially true in countries mainly culturing Japonica rice cultivars that do not have a gene conferring resistance to BPH, and where outbreaks of BHP are therefore a severe problem. The BPH causes direct damage to crops and indirect damage by acting as a vector for viral diseases. Chemical treatment is the conventional method of controlling pests such as BPH, even though it is expensive and harmful to the environment. Many researchers have reported that host plant resistance is the most effective way of controlling pests including BPH, and thus breeding of insect resistance has taken priority in rice improvement programs. Until now, 13BPH resistance genes, together with several quantitative trait loci (QTLs) controlling BPH resistance, have been reported in two wild relatives and indica cultivars. Diverse sources of BPH resistance have been identified and genetic analysis has revealed 6 dominant [Bph1, 3, 6, 9, 10, and 13(t)] and 7 recessive [bph2, 4, 5, 7, 8, 11(t), and 12(t)] genes controlling BPH resistance. Bph1, bph2, Bph9, and Bph10(t) were assigned to rice chromosome 12. Bph1 and bph2 confer resistance to biotypes 1, 3 and 1, 2 which are widely distributed in Southeast Asia. Many studies aimed at identifying BPH resistance genes have been conducted over the years in order to develop a resistant cultivar; however, a japonica cultivar with a BPH resistance gene has not yet been developed. Thirteen of the BPH resistance genes identified so far are not from japonica rice, but from indica rice. In bioassays, it has been reported that the reaction of early rice seedlings to BPH differed between japonica and indica. Japonica introgression lines with BPH resistance genes exhibited undesirable characteristics such as poor grain quality and lodging-related traits to which the resistance genes seemed to be highly linked. The undesirable linkage drag between a BPH resistance gene and genes conferring agriculturally important characters may be removed by intensive work to select recombinants between the traits, and a molecular marker tightly linked to the target gene could be useful for selecting the desired recombinants。&lt;br /&gt;
    The use of tightly linked genetic markers for resistance genes offers great scope for improving the efficiency of conventional plant breeding by allowing selection to be based on molecular markers linked to a trait at an early stage of growth, rather than being based on the trait itself. Resistance genes to gall midge and blast have been identified in rice, and linkage between DNA markers and these resistance genes has been analyzed. In this way linkage maps of genes associated with resistance to diseases and pests have been constructed in wheat, barley, and other economically important crops. The current study was conducted to identify Bph1-related DNA markers in rice, and thus to permit the establishment of a marker-assisted breeding program to introgress the BPH-resistance gene into japonica rice cultivars.&lt;br /&gt;
&lt;br /&gt;
== BPH Evalution ==&lt;br /&gt;
Brown planthopper (Nilaparvata lugens Stål.) is one of the most damaging pests of rice in Asia. It causes severe yield reduction by directly sucking the plant sap and acting as a vector of virus diseases such as rice grassy stunt and ragged stunt (Khush and Brar, 1991). Host plant resistance has been recognized as significant strategy to control BPH damage in contrast to the chemical control. The genetics of BPH resistance is well studied and as many as 21 major genes have been identified in cultivated and wild species (Qifa Zhang, 2007 and Fujita et al., 2008). Among the BPH biotypes prevailing in South East Asia, biotype 4 is the most destructive and distributed over the Indian subcontinent (Heinrichs, 1986). The biotype variations results in overcome of resistance to several major genes, therefore, the identification of additional BPH resistance genes is required to address the issue of durable resistance.&lt;br /&gt;
== Mapping of BPH gene ==&lt;br /&gt;
&lt;br /&gt;
 The repeated screening over the years of different donors with known gene, against local BPH biotype available at the Directorate of Rice Research, Hyderabad, India, recorded consistent resistance in Rathu Henati (Bph3 &amp;amp; Bph17), Swarnalatha (Bph 6) and ADR 52 (bph20(t) &amp;amp; Bph21(t)). While rest of other donors Mudgo (Bph1), IR 56 (Bph3), Pokkali (Bph9), IR 65482-4-136-2-2 (Bph10), IR 65482-7-216-1-2 (Bph18) showed either susceptible or moderate resistance(Table 1&amp;amp;Table 2).&lt;br /&gt;
[[File:Table 1.PNG]]&lt;br /&gt;
[[File:]]&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:Table_1.PNG&amp;diff=183820</id>
		<title>File:Table 1.PNG</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:Table_1.PNG&amp;diff=183820"/>
				<updated>2014-06-11T03:10:06Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=BPH_gene&amp;diff=183818</id>
		<title>BPH gene</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=BPH_gene&amp;diff=183818"/>
				<updated>2014-06-11T03:04:59Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;    The brown planthopper (BPH), Nilaparvata lugens, is one of the most serious insect pests throughout rice growing areas in Asia. This is especially true in countries mainly culturing Japonica rice cultivars that do not have a gene conferring resistance to BPH, and where outbreaks of BHP are therefore a severe problem. The BPH causes direct damage to crops and indirect damage by acting as a vector for viral diseases. Chemical treatment is the conventional method of controlling pests such as BPH, even though it is expensive and harmful to the environment. Many researchers have reported that host plant resistance is the most effective way of controlling pests including BPH, and thus breeding of insect resistance has taken priority in rice improvement programs. Until now, 13BPH resistance genes, together with several quantitative trait loci (QTLs) controlling BPH resistance, have been reported in two wild relatives and indica cultivars. Diverse sources of BPH resistance have been identified and genetic analysis has revealed 6 dominant [Bph1, 3, 6, 9, 10, and 13(t)] and 7 recessive [bph2, 4, 5, 7, 8, 11(t), and 12(t)] genes controlling BPH resistance. Bph1, bph2, Bph9, and Bph10(t) were assigned to rice chromosome 12. Bph1 and bph2 confer resistance to biotypes 1, 3 and 1, 2 which are widely distributed in Southeast Asia. Many studies aimed at identifying BPH resistance genes have been conducted over the years in order to develop a resistant cultivar; however, a japonica cultivar with a BPH resistance gene has not yet been developed. Thirteen of the BPH resistance genes identified so far are not from japonica rice, but from indica rice. In bioassays, it has been reported that the reaction of early rice seedlings to BPH differed between japonica and indica. Japonica introgression lines with BPH resistance genes exhibited undesirable characteristics such as poor grain quality and lodging-related traits to which the resistance genes seemed to be highly linked. The undesirable linkage drag between a BPH resistance gene and genes conferring agriculturally important characters may be removed by intensive work to select recombinants between the traits, and a molecular marker tightly linked to the target gene could be useful for selecting the desired recombinants。&lt;br /&gt;
    The use of tightly linked genetic markers for resistance genes offers great scope for improving the efficiency of conventional plant breeding by allowing selection to be based on molecular markers linked to a trait at an early stage of growth, rather than being based on the trait itself. Resistance genes to gall midge and blast have been identified in rice, and linkage between DNA markers and these resistance genes has been analyzed. In this way linkage maps of genes associated with resistance to diseases and pests have been constructed in wheat, barley, and other economically important crops. The current study was conducted to identify Bph1-related DNA markers in rice, and thus to permit the establishment of a marker-assisted breeding program to introgress the BPH-resistance gene into japonica rice cultivars.&lt;br /&gt;
&lt;br /&gt;
== BPH Evalution ==&lt;br /&gt;
Brown planthopper (Nilaparvata lugens Stål.) is one of the most damaging pests of rice in Asia. It causes severe yield reduction by directly sucking the plant sap and acting as a vector of virus diseases such as rice grassy stunt and ragged stunt (Khush and Brar, 1991). Host plant resistance has been recognized as significant strategy to control BPH damage in contrast to the chemical control. The genetics of BPH resistance is well studied and as many as 21 major genes have been identified in cultivated and wild species (Qifa Zhang, 2007 and Fujita et al., 2008). Among the BPH biotypes prevailing in South East Asia, biotype 4 is the most destructive and distributed over the Indian subcontinent (Heinrichs, 1986). The biotype variations results in overcome of resistance to several major genes, therefore, the identification of additional BPH resistance genes is required to address the issue of durable resistance.&lt;br /&gt;
== Mapping of BPH gene ==&lt;br /&gt;
&lt;br /&gt;
 The repeated screening over the years of different donors with known gene, against local BPH biotype available at the Directorate of Rice Research, Hyderabad, India, recorded consistent resistance in Rathu Henati (Bph3 &amp;amp; Bph17), Swarnalatha (Bph 6) and ADR 52 (bph20(t) &amp;amp; Bph21(t)). While rest of other donors Mudgo (Bph1), IR 56 (Bph3), Pokkali (Bph9), IR 65482-4-136-2-2 (Bph10), IR 65482-7-216-1-2 (Bph18) showed either susceptible or moderate resistance&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph27&amp;diff=182008</id>
		<title>Bph27</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph27&amp;diff=182008"/>
				<updated>2014-06-09T07:51:39Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* References */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
== Background ==&lt;br /&gt;
The brown planthopper (Nilaparvata lugens Stål; BPH) is one of the most hazardous rice pests in the world. Growing resistant varieties is the most active way to deal with this insect, and wild rice species are a valuable source of resistance genes for developing resistant cultivars. BPH27 derived from an accession of Guangxi wild rice, Oryza rufipogon Griff. (Accession no. 2183, hereafter named GX2183), was primarily mapped to a 17-cM region on the long arm of the chromosome four. Furthermore, fine mapping of BPH27 was conducted using two BC1F2 populations derived from introgression lines of GX2183. Insect resistance was assessed in the BC1F2 populations with 6,010 individual off springs, and 346 resistance extremes were obtained and employed for fine mapping of BPH27. High-resolution linkage analysis discover the BPH27 locus to an 86.3-kb region in Nipponbare.&lt;br /&gt;
&lt;br /&gt;
== Damage caused by brown planthopper==&lt;br /&gt;
[[File:危害.PNG]]&lt;br /&gt;
&lt;br /&gt;
== Mapping ==&lt;br /&gt;
[[File:The pedigree.PNG]]&lt;br /&gt;
[[File:SSR makers.PNG]]&lt;br /&gt;
[[File:Location.PNG ]]&lt;br /&gt;
[[File:Region.PNG ‎ ]]&lt;br /&gt;
[[File:Region2.PNG ]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Possible nature of BPH27 ==&lt;br /&gt;
&lt;br /&gt;
It is now known that the responses of rice to BPH feeding are most possibly similar to pathogen-defense responses (Wang et al. 2008; Du et al. 2009). For example, Bph14 is a member of the coiled-coil, nucleotide-binding, and leucinerich repeat (CC-NB-LRR) disease resistance gene family and provides resistance to BPH in a mechanism fundamentally similar to defense mechanisms against pathogens by activating an SA-dependent pathway (Du et al. 2009). The chromosome region containing BPH27 is rich in genes involved in disease response. Three predicted genes, LOC_Os04g31924, LOC_Os04g32000 and ORF12 of 93-11, are likely involved in response to disease and thus are considered the primary candidates of the BPH27 gene.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Potential use of BPH-resistance genes for rice improvement ==&lt;br /&gt;
&lt;br /&gt;
Compared with dominant resistance genes to BPH, little progress has been made in recessive resistance genes. Fine mapping of BPH27 on chromosome 4, therefore, provides valuable information for understanding the molecular mechanisms underlying the recessive gene-mediated resistance. Candidate genes in the fine-mapped region by sequencing parental lines and transforming susceptible parent with cloned BPH27 candidate genes still need to be vindicated. Moreover, a number of simple molecular markers will be exploited to support in the development of rice cultivars that are resistant to multiple BPH biotypes.&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1.	D. Huang • Y. Qiu • Y. Zhang • F. Huang •J. Meng • S. Wei • R. Li • B. Chen Fine mapping and characterization of BPH27, a brown planthopper resistance gene from wild rice. Theor Appl Genet (2013) 126:219–229&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
2.	Wang YY, Wang XL, Yuan HY, Chen RZ, Zhu LL, He RF, He GC (2008) Responses of two contrasting genotypes of rice to brown planthopper. Mol Plant Microbe Interact 21:122–132&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
3.	Du B, Zhang WL, Liu BF, Hu J, Wei Z, Shi ZY, He RF, Zhu LL, Chen RZ, Han B, He GC (2009) Identification and characterization of Bph14, a gene conferring resistance to brown planthopper in rice. Proc Natl Acad Sci USA 106(52):22163–22168&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph27&amp;diff=182003</id>
		<title>Bph27</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph27&amp;diff=182003"/>
				<updated>2014-06-09T07:49:46Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* Potential use of BPH-resistance genes for rice improvement */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
== Background ==&lt;br /&gt;
The brown planthopper (Nilaparvata lugens Stål; BPH) is one of the most hazardous rice pests in the world. Growing resistant varieties is the most active way to deal with this insect, and wild rice species are a valuable source of resistance genes for developing resistant cultivars. BPH27 derived from an accession of Guangxi wild rice, Oryza rufipogon Griff. (Accession no. 2183, hereafter named GX2183), was primarily mapped to a 17-cM region on the long arm of the chromosome four. Furthermore, fine mapping of BPH27 was conducted using two BC1F2 populations derived from introgression lines of GX2183. Insect resistance was assessed in the BC1F2 populations with 6,010 individual off springs, and 346 resistance extremes were obtained and employed for fine mapping of BPH27. High-resolution linkage analysis discover the BPH27 locus to an 86.3-kb region in Nipponbare.&lt;br /&gt;
&lt;br /&gt;
== Damage caused by brown planthopper==&lt;br /&gt;
[[File:危害.PNG]]&lt;br /&gt;
&lt;br /&gt;
== Mapping ==&lt;br /&gt;
[[File:The pedigree.PNG]]&lt;br /&gt;
[[File:SSR makers.PNG]]&lt;br /&gt;
[[File:Location.PNG ]]&lt;br /&gt;
[[File:Region.PNG ‎ ]]&lt;br /&gt;
[[File:Region2.PNG ]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Possible nature of BPH27 ==&lt;br /&gt;
&lt;br /&gt;
It is now known that the responses of rice to BPH feeding are most possibly similar to pathogen-defense responses (Wang et al. 2008; Du et al. 2009). For example, Bph14 is a member of the coiled-coil, nucleotide-binding, and leucinerich repeat (CC-NB-LRR) disease resistance gene family and provides resistance to BPH in a mechanism fundamentally similar to defense mechanisms against pathogens by activating an SA-dependent pathway (Du et al. 2009). The chromosome region containing BPH27 is rich in genes involved in disease response. Three predicted genes, LOC_Os04g31924, LOC_Os04g32000 and ORF12 of 93-11, are likely involved in response to disease and thus are considered the primary candidates of the BPH27 gene.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Potential use of BPH-resistance genes for rice improvement ==&lt;br /&gt;
&lt;br /&gt;
Compared with dominant resistance genes to BPH, little progress has been made in recessive resistance genes. Fine mapping of BPH27 on chromosome 4, therefore, provides valuable information for understanding the molecular mechanisms underlying the recessive gene-mediated resistance. Candidate genes in the fine-mapped region by sequencing parental lines and transforming susceptible parent with cloned BPH27 candidate genes still need to be vindicated. Moreover, a number of simple molecular markers will be exploited to support in the development of rice cultivars that are resistant to multiple BPH biotypes.&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1.	D. Huang • Y. Qiu • Y. Zhang • F. Huang •J. Meng • S. Wei • R. Li • B. Chen Fine mapping and characterization of BPH27, a brown planthopper resistance gene from wild rice. Theor Appl Genet (2013) 126:219–229&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph27&amp;diff=181993</id>
		<title>Bph27</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph27&amp;diff=181993"/>
				<updated>2014-06-09T07:44:50Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* References */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
== Background ==&lt;br /&gt;
The brown planthopper (Nilaparvata lugens Stål; BPH) is one of the most hazardous rice pests in the world. Growing resistant varieties is the most active way to deal with this insect, and wild rice species are a valuable source of resistance genes for developing resistant cultivars. BPH27 derived from an accession of Guangxi wild rice, Oryza rufipogon Griff. (Accession no. 2183, hereafter named GX2183), was primarily mapped to a 17-cM region on the long arm of the chromosome four. Furthermore, fine mapping of BPH27 was conducted using two BC1F2 populations derived from introgression lines of GX2183. Insect resistance was assessed in the BC1F2 populations with 6,010 individual off springs, and 346 resistance extremes were obtained and employed for fine mapping of BPH27. High-resolution linkage analysis discover the BPH27 locus to an 86.3-kb region in Nipponbare.&lt;br /&gt;
&lt;br /&gt;
== Damage caused by brown planthopper==&lt;br /&gt;
[[File:危害.PNG]]&lt;br /&gt;
&lt;br /&gt;
== Mapping ==&lt;br /&gt;
[[File:The pedigree.PNG]]&lt;br /&gt;
[[File:SSR makers.PNG]]&lt;br /&gt;
[[File:Location.PNG ]]&lt;br /&gt;
[[File:Region.PNG ‎ ]]&lt;br /&gt;
[[File:Region2.PNG ]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Potential use of BPH-resistance genes for rice improvement ==&lt;br /&gt;
&lt;br /&gt;
Compared with dominant resistance genes to BPH, little progress has been made in recessive resistance genes. Fine mapping of BPH27 on chromosome 4, therefore, provides valuable information for understanding the molecular mechanisms underlying the recessive gene-mediated resistance. Candidate genes in the fine-mapped region by sequencing parental lines and transforming susceptible parent with cloned BPH27 candidate genes still need to be vindicated. Moreover, a number of simple molecular markers will be exploited to support in the development of rice cultivars that are resistant to multiple BPH biotypes.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1.	D. Huang • Y. Qiu • Y. Zhang • F. Huang •J. Meng • S. Wei • R. Li • B. Chen Fine mapping and characterization of BPH27, a brown planthopper resistance gene from wild rice. Theor Appl Genet (2013) 126:219–229&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph27&amp;diff=181988</id>
		<title>Bph27</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph27&amp;diff=181988"/>
				<updated>2014-06-09T07:37:05Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* Mapping */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
== Background ==&lt;br /&gt;
The brown planthopper (Nilaparvata lugens Stål; BPH) is one of the most hazardous rice pests in the world. Growing resistant varieties is the most active way to deal with this insect, and wild rice species are a valuable source of resistance genes for developing resistant cultivars. BPH27 derived from an accession of Guangxi wild rice, Oryza rufipogon Griff. (Accession no. 2183, hereafter named GX2183), was primarily mapped to a 17-cM region on the long arm of the chromosome four. Furthermore, fine mapping of BPH27 was conducted using two BC1F2 populations derived from introgression lines of GX2183. Insect resistance was assessed in the BC1F2 populations with 6,010 individual off springs, and 346 resistance extremes were obtained and employed for fine mapping of BPH27. High-resolution linkage analysis discover the BPH27 locus to an 86.3-kb region in Nipponbare.&lt;br /&gt;
&lt;br /&gt;
== Damage caused by brown planthopper==&lt;br /&gt;
[[File:危害.PNG]]&lt;br /&gt;
&lt;br /&gt;
== Mapping ==&lt;br /&gt;
[[File:The pedigree.PNG]]&lt;br /&gt;
[[File:SSR makers.PNG]]&lt;br /&gt;
[[File:Location.PNG ]]&lt;br /&gt;
[[File:Region.PNG ‎ ]]&lt;br /&gt;
[[File:Region2.PNG ]]&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1.	D. Huang • Y. Qiu • Y. Zhang • F. Huang •J. Meng • S. Wei • R. Li • B. Chen Fine mapping and characterization of BPH27, a brown planthopper resistance gene from wild rice. Theor Appl Genet (2013) 126:219–229&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:SSR_makers.PNG&amp;diff=181987</id>
		<title>File:SSR makers.PNG</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:SSR_makers.PNG&amp;diff=181987"/>
				<updated>2014-06-09T07:36:00Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: uploaded a new version of &amp;amp;quot;File:SSR makers.PNG&amp;amp;quot;&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:The_pedigree.PNG&amp;diff=181977</id>
		<title>File:The pedigree.PNG</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:The_pedigree.PNG&amp;diff=181977"/>
				<updated>2014-06-09T07:32:02Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:SSR_makers.PNG&amp;diff=181976</id>
		<title>File:SSR makers.PNG</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:SSR_makers.PNG&amp;diff=181976"/>
				<updated>2014-06-09T07:31:48Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:Region2.PNG&amp;diff=181975</id>
		<title>File:Region2.PNG</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:Region2.PNG&amp;diff=181975"/>
				<updated>2014-06-09T07:31:34Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:Region.PNG&amp;diff=181973</id>
		<title>File:Region.PNG</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:Region.PNG&amp;diff=181973"/>
				<updated>2014-06-09T07:31:06Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:Location.PNG&amp;diff=181972</id>
		<title>File:Location.PNG</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:Location.PNG&amp;diff=181972"/>
				<updated>2014-06-09T07:30:47Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph27&amp;diff=181970</id>
		<title>Bph27</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph27&amp;diff=181970"/>
				<updated>2014-06-09T07:29:39Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* Mapping */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
== Background ==&lt;br /&gt;
The brown planthopper (Nilaparvata lugens Stål; BPH) is one of the most hazardous rice pests in the world. Growing resistant varieties is the most active way to deal with this insect, and wild rice species are a valuable source of resistance genes for developing resistant cultivars. BPH27 derived from an accession of Guangxi wild rice, Oryza rufipogon Griff. (Accession no. 2183, hereafter named GX2183), was primarily mapped to a 17-cM region on the long arm of the chromosome four. Furthermore, fine mapping of BPH27 was conducted using two BC1F2 populations derived from introgression lines of GX2183. Insect resistance was assessed in the BC1F2 populations with 6,010 individual off springs, and 346 resistance extremes were obtained and employed for fine mapping of BPH27. High-resolution linkage analysis discover the BPH27 locus to an 86.3-kb region in Nipponbare.&lt;br /&gt;
&lt;br /&gt;
== Damage caused by brown planthopper==&lt;br /&gt;
[[File:危害.PNG]]&lt;br /&gt;
&lt;br /&gt;
== Mapping ==&lt;br /&gt;
[[File:]]&lt;br /&gt;
[[File:]]&lt;br /&gt;
[[File:]]&lt;br /&gt;
[[File:]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
1.	D. Huang • Y. Qiu • Y. Zhang • F. Huang •J. Meng • S. Wei • R. Li • B. Chen Fine mapping and characterization of BPH27, a brown planthopper resistance gene from wild rice. Theor Appl Genet (2013) 126:219–229&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph27&amp;diff=181960</id>
		<title>Bph27</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph27&amp;diff=181960"/>
				<updated>2014-06-09T07:15:34Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* Damage caused by brown planthopper */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
== Background ==&lt;br /&gt;
The brown planthopper (Nilaparvata lugens Stål; BPH) is one of the most hazardous rice pests in the world. Growing resistant varieties is the most active way to deal with this insect, and wild rice species are a valuable source of resistance genes for developing resistant cultivars. BPH27 derived from an accession of Guangxi wild rice, Oryza rufipogon Griff. (Accession no. 2183, hereafter named GX2183), was primarily mapped to a 17-cM region on the long arm of the chromosome four. Furthermore, fine mapping of BPH27 was conducted using two BC1F2 populations derived from introgression lines of GX2183. Insect resistance was assessed in the BC1F2 populations with 6,010 individual off springs, and 346 resistance extremes were obtained and employed for fine mapping of BPH27. High-resolution linkage analysis discover the BPH27 locus to an 86.3-kb region in Nipponbare.&lt;br /&gt;
&lt;br /&gt;
== Damage caused by brown planthopper==&lt;br /&gt;
[[File:危害.PNG]]&lt;br /&gt;
&lt;br /&gt;
== Mapping ==&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:%E5%8D%B1%E5%AE%B3.PNG&amp;diff=181958</id>
		<title>File:危害.PNG</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:%E5%8D%B1%E5%AE%B3.PNG&amp;diff=181958"/>
				<updated>2014-06-09T07:14:40Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph27&amp;diff=181953</id>
		<title>Bph27</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph27&amp;diff=181953"/>
				<updated>2014-06-09T07:12:43Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* Mapping */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
== Background ==&lt;br /&gt;
The brown planthopper (Nilaparvata lugens Stål; BPH) is one of the most hazardous rice pests in the world. Growing resistant varieties is the most active way to deal with this insect, and wild rice species are a valuable source of resistance genes for developing resistant cultivars. BPH27 derived from an accession of Guangxi wild rice, Oryza rufipogon Griff. (Accession no. 2183, hereafter named GX2183), was primarily mapped to a 17-cM region on the long arm of the chromosome four. Furthermore, fine mapping of BPH27 was conducted using two BC1F2 populations derived from introgression lines of GX2183. Insect resistance was assessed in the BC1F2 populations with 6,010 individual off springs, and 346 resistance extremes were obtained and employed for fine mapping of BPH27. High-resolution linkage analysis discover the BPH27 locus to an 86.3-kb region in Nipponbare.&lt;br /&gt;
&lt;br /&gt;
== Damage caused by brown planthopper==&lt;br /&gt;
[[File:]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Mapping ==&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph27&amp;diff=181738</id>
		<title>Bph27</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph27&amp;diff=181738"/>
				<updated>2014-06-09T04:24:58Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: Created page with &amp;quot; == Mapping ==&amp;quot;&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
== Mapping ==&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181735</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181735"/>
				<updated>2014-06-09T04:23:38Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* Reference */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
== Background ==&lt;br /&gt;
&lt;br /&gt;
Genetic and breeding research on the natural resistance system against a serious insect pest of rice, brown planthopper (BPH), Nilaparvata lugens Stal, begun in the mid-1960s. Twelve BPH resistance genes have so far been identified. A BPH resistance gene, Bph10, from Oryza australiensis was first assigned to rice chromosome 12 (Ishii et al. 1994). Later, Bph1from an Indian variety, Mudgo, and bph2 from an IRRI breeding line, IR1154-243, were also mapped on chromosome 12 (Hirabayashi and Ogawa 1995; Murata et al. 1997, 1998).Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000).&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Functions of BPH ==&lt;br /&gt;
The brown planthopper (BPH) is one of the most devastating insect pests of rice in Asia. BPH is a sap-feeding insect that causes &amp;quot;hopper-burn&amp;quot; and could also be a vector for rice grassy stunt virus and ragged stunt virus. Use of pesticides to combat this pest is costly and could also cause the decrease in the population of other beneficial insects in the field. Rice variety Shanyou 63, which was widely cultivated in China, has decreased in production due to its susceptibility to pests such as BPH.&lt;br /&gt;
&lt;br /&gt;
==The discovery of Bph9 map position ==&lt;br /&gt;
&lt;br /&gt;
Pokkali, because Norin-PL9 was known to be cross-compatible with indica varieties. Contrary to the expectation, however, this japonica-indica cross resulted in highly sterile F1s and F2s. Ten F3 plants were grown from each of 98 F2 individuals but only 65 F3 families with enough numbers of F4 seeds for bioassay were obtained. Genotypes of 62 F3 families thus 62 F2individuals for BPH resistance/susceptibility were determined by bioassay of F4 families according to the previously described method (Murata et al. 1998). The heterozygous F3s had 70-75 % resistant F4 progenies, agreeing with that Bph9 was dominant. The segregation ratio in 62 F2s was 12 RR:33 RS:17 SS, which did not deviate from the expected single gene control of resistance. &lt;br /&gt;
&lt;br /&gt;
DNA was extracted from an equal amount (8 g) of leaves of 10 F3 plants derived from each F2 individual. DNA bulks were further prepared by combining four F3 families (each with 10 F3 plants) with RR and SS genotypes, respectively. A total of 106 RFLP markers and eight restriction enzymes were used for the bulked segregant analysis. In addition, a total of 240 random 10-mer primers (Operon Technologies) were surveyed in RAPD-PCR analysis.&lt;br /&gt;
&lt;br /&gt;
Segregation of seven RFLP and two RAPD markers in the 62 F2 plants did not deviate from the expected 1:2:1 ratio or 1:3 ratio. The result indicated no apparent segregation distortion in the chromosomal region covering the Bph9 locus, despite the observed high sterility in this cross combination. Recombination values were calculated by MAPMAKER Version 2.0 with LOD scores greater than 3.0. These markers and Bph9 were located in the 53 cM segment, which was delimited by two RFLP markers (R617 and 1709) on the long arm of chromosome 12 (Fig. 1). A RAPD marker (OPR04) was found to be closest, with a map distance of 8.8 cM from the Bph9 locus. The map distance between the two RFLP markers (G2140 and S2545), however, was much greater than the corresponding distance on the standard Nipponbare/Kasalath map. This might be ascribed either to the use of different mapping populations or to the smaller population size and high sterility in the present cross.&lt;br /&gt;
&lt;br /&gt;
== Map position ==&lt;br /&gt;
&lt;br /&gt;
[[File:QQ图片20140608222722.jpg]]&lt;br /&gt;
&lt;br /&gt;
== Reference ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181733</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181733"/>
				<updated>2014-06-09T04:22:29Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* Background */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
== Background ==&lt;br /&gt;
&lt;br /&gt;
Genetic and breeding research on the natural resistance system against a serious insect pest of rice, brown planthopper (BPH), Nilaparvata lugens Stal, begun in the mid-1960s. Twelve BPH resistance genes have so far been identified. A BPH resistance gene, Bph10, from Oryza australiensis was first assigned to rice chromosome 12 (Ishii et al. 1994). Later, Bph1from an Indian variety, Mudgo, and bph2 from an IRRI breeding line, IR1154-243, were also mapped on chromosome 12 (Hirabayashi and Ogawa 1995; Murata et al. 1997, 1998).Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000).&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Functions of BPH ==&lt;br /&gt;
The brown planthopper (BPH) is one of the most devastating insect pests of rice in Asia. BPH is a sap-feeding insect that causes &amp;quot;hopper-burn&amp;quot; and could also be a vector for rice grassy stunt virus and ragged stunt virus. Use of pesticides to combat this pest is costly and could also cause the decrease in the population of other beneficial insects in the field. Rice variety Shanyou 63, which was widely cultivated in China, has decreased in production due to its susceptibility to pests such as BPH.&lt;br /&gt;
&lt;br /&gt;
==The discovery of Bph9 map position ==&lt;br /&gt;
&lt;br /&gt;
Pokkali, because Norin-PL9 was known to be cross-compatible with indica varieties. Contrary to the expectation, however, this japonica-indica cross resulted in highly sterile F1s and F2s. Ten F3 plants were grown from each of 98 F2 individuals but only 65 F3 families with enough numbers of F4 seeds for bioassay were obtained. Genotypes of 62 F3 families thus 62 F2individuals for BPH resistance/susceptibility were determined by bioassay of F4 families according to the previously described method (Murata et al. 1998). The heterozygous F3s had 70-75 % resistant F4 progenies, agreeing with that Bph9 was dominant. The segregation ratio in 62 F2s was 12 RR:33 RS:17 SS, which did not deviate from the expected single gene control of resistance. &lt;br /&gt;
&lt;br /&gt;
DNA was extracted from an equal amount (8 g) of leaves of 10 F3 plants derived from each F2 individual. DNA bulks were further prepared by combining four F3 families (each with 10 F3 plants) with RR and SS genotypes, respectively. A total of 106 RFLP markers and eight restriction enzymes were used for the bulked segregant analysis. In addition, a total of 240 random 10-mer primers (Operon Technologies) were surveyed in RAPD-PCR analysis.&lt;br /&gt;
&lt;br /&gt;
Segregation of seven RFLP and two RAPD markers in the 62 F2 plants did not deviate from the expected 1:2:1 ratio or 1:3 ratio. The result indicated no apparent segregation distortion in the chromosomal region covering the Bph9 locus, despite the observed high sterility in this cross combination. Recombination values were calculated by MAPMAKER Version 2.0 with LOD scores greater than 3.0. These markers and Bph9 were located in the 53 cM segment, which was delimited by two RFLP markers (R617 and 1709) on the long arm of chromosome 12 (Fig. 1). A RAPD marker (OPR04) was found to be closest, with a map distance of 8.8 cM from the Bph9 locus. The map distance between the two RFLP markers (G2140 and S2545), however, was much greater than the corresponding distance on the standard Nipponbare/Kasalath map. This might be ascribed either to the use of different mapping populations or to the smaller population size and high sterility in the present cross.&lt;br /&gt;
&lt;br /&gt;
== Map position ==&lt;br /&gt;
&lt;br /&gt;
[[File:QQ图片20140608222722.jpg]]&lt;br /&gt;
&lt;br /&gt;
== Reference ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål, in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181713</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181713"/>
				<updated>2014-06-09T04:09:38Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* 【Reference】 */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
== Background ==&lt;br /&gt;
&lt;br /&gt;
Genetic and breeding research on the natural resistance system against a serious insect pest of rice, brown planthopper (BPH), Nilaparvata lugens Stal, begun in the mid-1960s. Twelve BPH resistance genes have so far been identified. A BPH resistance gene, Bph10, from Oryza australiensis was first assigned to rice chromosome 12 (Ishii et al. 1994). Later, Bph1from an Indian variety, Mudgo, and bph2 from an IRRI breeding line, IR1154-243, were also mapped on chromosome 12 (Hirabayashi and Ogawa 1995; Murata et al. 1997, 1998).Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000).&lt;br /&gt;
&lt;br /&gt;
==The discovery of Bph9 map position ==&lt;br /&gt;
&lt;br /&gt;
Pokkali, because Norin-PL9 was known to be cross-compatible with indica varieties. Contrary to the expectation, however, this japonica-indica cross resulted in highly sterile F1s and F2s. Ten F3 plants were grown from each of 98 F2 individuals but only 65 F3 families with enough numbers of F4 seeds for bioassay were obtained. Genotypes of 62 F3 families thus 62 F2individuals for BPH resistance/susceptibility were determined by bioassay of F4 families according to the previously described method (Murata et al. 1998). The heterozygous F3s had 70-75 % resistant F4 progenies, agreeing with that Bph9 was dominant. The segregation ratio in 62 F2s was 12 RR:33 RS:17 SS, which did not deviate from the expected single gene control of resistance. &lt;br /&gt;
&lt;br /&gt;
DNA was extracted from an equal amount (8 g) of leaves of 10 F3 plants derived from each F2 individual. DNA bulks were further prepared by combining four F3 families (each with 10 F3 plants) with RR and SS genotypes, respectively. A total of 106 RFLP markers and eight restriction enzymes were used for the bulked segregant analysis. In addition, a total of 240 random 10-mer primers (Operon Technologies) were surveyed in RAPD-PCR analysis.&lt;br /&gt;
&lt;br /&gt;
Segregation of seven RFLP and two RAPD markers in the 62 F2 plants did not deviate from the expected 1:2:1 ratio or 1:3 ratio. The result indicated no apparent segregation distortion in the chromosomal region covering the Bph9 locus, despite the observed high sterility in this cross combination. Recombination values were calculated by MAPMAKER Version 2.0 with LOD scores greater than 3.0. These markers and Bph9 were located in the 53 cM segment, which was delimited by two RFLP markers (R617 and 1709) on the long arm of chromosome 12 (Fig. 1). A RAPD marker (OPR04) was found to be closest, with a map distance of 8.8 cM from the Bph9 locus. The map distance between the two RFLP markers (G2140 and S2545), however, was much greater than the corresponding distance on the standard Nipponbare/Kasalath map. This might be ascribed either to the use of different mapping populations or to the smaller population size and high sterility in the present cross.&lt;br /&gt;
&lt;br /&gt;
== Map position ==&lt;br /&gt;
&lt;br /&gt;
[[File:QQ图片20140608222722.jpg]]&lt;br /&gt;
&lt;br /&gt;
== Reference ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål, in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181712</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181712"/>
				<updated>2014-06-09T04:09:25Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* 【Map position】 */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
== Background ==&lt;br /&gt;
&lt;br /&gt;
Genetic and breeding research on the natural resistance system against a serious insect pest of rice, brown planthopper (BPH), Nilaparvata lugens Stal, begun in the mid-1960s. Twelve BPH resistance genes have so far been identified. A BPH resistance gene, Bph10, from Oryza australiensis was first assigned to rice chromosome 12 (Ishii et al. 1994). Later, Bph1from an Indian variety, Mudgo, and bph2 from an IRRI breeding line, IR1154-243, were also mapped on chromosome 12 (Hirabayashi and Ogawa 1995; Murata et al. 1997, 1998).Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000).&lt;br /&gt;
&lt;br /&gt;
==The discovery of Bph9 map position ==&lt;br /&gt;
&lt;br /&gt;
Pokkali, because Norin-PL9 was known to be cross-compatible with indica varieties. Contrary to the expectation, however, this japonica-indica cross resulted in highly sterile F1s and F2s. Ten F3 plants were grown from each of 98 F2 individuals but only 65 F3 families with enough numbers of F4 seeds for bioassay were obtained. Genotypes of 62 F3 families thus 62 F2individuals for BPH resistance/susceptibility were determined by bioassay of F4 families according to the previously described method (Murata et al. 1998). The heterozygous F3s had 70-75 % resistant F4 progenies, agreeing with that Bph9 was dominant. The segregation ratio in 62 F2s was 12 RR:33 RS:17 SS, which did not deviate from the expected single gene control of resistance. &lt;br /&gt;
&lt;br /&gt;
DNA was extracted from an equal amount (8 g) of leaves of 10 F3 plants derived from each F2 individual. DNA bulks were further prepared by combining four F3 families (each with 10 F3 plants) with RR and SS genotypes, respectively. A total of 106 RFLP markers and eight restriction enzymes were used for the bulked segregant analysis. In addition, a total of 240 random 10-mer primers (Operon Technologies) were surveyed in RAPD-PCR analysis.&lt;br /&gt;
&lt;br /&gt;
Segregation of seven RFLP and two RAPD markers in the 62 F2 plants did not deviate from the expected 1:2:1 ratio or 1:3 ratio. The result indicated no apparent segregation distortion in the chromosomal region covering the Bph9 locus, despite the observed high sterility in this cross combination. Recombination values were calculated by MAPMAKER Version 2.0 with LOD scores greater than 3.0. These markers and Bph9 were located in the 53 cM segment, which was delimited by two RFLP markers (R617 and 1709) on the long arm of chromosome 12 (Fig. 1). A RAPD marker (OPR04) was found to be closest, with a map distance of 8.8 cM from the Bph9 locus. The map distance between the two RFLP markers (G2140 and S2545), however, was much greater than the corresponding distance on the standard Nipponbare/Kasalath map. This might be ascribed either to the use of different mapping populations or to the smaller population size and high sterility in the present cross.&lt;br /&gt;
&lt;br /&gt;
== Map position ==&lt;br /&gt;
&lt;br /&gt;
[[File:QQ图片20140608222722.jpg]]&lt;br /&gt;
&lt;br /&gt;
== 【Reference】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål, in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181711</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181711"/>
				<updated>2014-06-09T04:08:53Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* 【The discovery of Bph9 map position】 */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
== Background ==&lt;br /&gt;
&lt;br /&gt;
Genetic and breeding research on the natural resistance system against a serious insect pest of rice, brown planthopper (BPH), Nilaparvata lugens Stal, begun in the mid-1960s. Twelve BPH resistance genes have so far been identified. A BPH resistance gene, Bph10, from Oryza australiensis was first assigned to rice chromosome 12 (Ishii et al. 1994). Later, Bph1from an Indian variety, Mudgo, and bph2 from an IRRI breeding line, IR1154-243, were also mapped on chromosome 12 (Hirabayashi and Ogawa 1995; Murata et al. 1997, 1998).Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000).&lt;br /&gt;
&lt;br /&gt;
==The discovery of Bph9 map position ==&lt;br /&gt;
&lt;br /&gt;
Pokkali, because Norin-PL9 was known to be cross-compatible with indica varieties. Contrary to the expectation, however, this japonica-indica cross resulted in highly sterile F1s and F2s. Ten F3 plants were grown from each of 98 F2 individuals but only 65 F3 families with enough numbers of F4 seeds for bioassay were obtained. Genotypes of 62 F3 families thus 62 F2individuals for BPH resistance/susceptibility were determined by bioassay of F4 families according to the previously described method (Murata et al. 1998). The heterozygous F3s had 70-75 % resistant F4 progenies, agreeing with that Bph9 was dominant. The segregation ratio in 62 F2s was 12 RR:33 RS:17 SS, which did not deviate from the expected single gene control of resistance. &lt;br /&gt;
&lt;br /&gt;
DNA was extracted from an equal amount (8 g) of leaves of 10 F3 plants derived from each F2 individual. DNA bulks were further prepared by combining four F3 families (each with 10 F3 plants) with RR and SS genotypes, respectively. A total of 106 RFLP markers and eight restriction enzymes were used for the bulked segregant analysis. In addition, a total of 240 random 10-mer primers (Operon Technologies) were surveyed in RAPD-PCR analysis.&lt;br /&gt;
&lt;br /&gt;
Segregation of seven RFLP and two RAPD markers in the 62 F2 plants did not deviate from the expected 1:2:1 ratio or 1:3 ratio. The result indicated no apparent segregation distortion in the chromosomal region covering the Bph9 locus, despite the observed high sterility in this cross combination. Recombination values were calculated by MAPMAKER Version 2.0 with LOD scores greater than 3.0. These markers and Bph9 were located in the 53 cM segment, which was delimited by two RFLP markers (R617 and 1709) on the long arm of chromosome 12 (Fig. 1). A RAPD marker (OPR04) was found to be closest, with a map distance of 8.8 cM from the Bph9 locus. The map distance between the two RFLP markers (G2140 and S2545), however, was much greater than the corresponding distance on the standard Nipponbare/Kasalath map. This might be ascribed either to the use of different mapping populations or to the smaller population size and high sterility in the present cross.&lt;br /&gt;
&lt;br /&gt;
== 【Map position】 ==&lt;br /&gt;
&lt;br /&gt;
[[File:QQ图片20140608222722.jpg]]&lt;br /&gt;
&lt;br /&gt;
== 【Reference】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål, in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181710</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181710"/>
				<updated>2014-06-09T04:08:29Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* 【Background】 */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
== Background ==&lt;br /&gt;
&lt;br /&gt;
Genetic and breeding research on the natural resistance system against a serious insect pest of rice, brown planthopper (BPH), Nilaparvata lugens Stal, begun in the mid-1960s. Twelve BPH resistance genes have so far been identified. A BPH resistance gene, Bph10, from Oryza australiensis was first assigned to rice chromosome 12 (Ishii et al. 1994). Later, Bph1from an Indian variety, Mudgo, and bph2 from an IRRI breeding line, IR1154-243, were also mapped on chromosome 12 (Hirabayashi and Ogawa 1995; Murata et al. 1997, 1998).Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000).&lt;br /&gt;
&lt;br /&gt;
==【The discovery of Bph9 map position】 ==&lt;br /&gt;
&lt;br /&gt;
Pokkali, because Norin-PL9 was known to be cross-compatible with indica varieties. Contrary to the expectation, however, this japonica-indica cross resulted in highly sterile F1s and F2s. Ten F3 plants were grown from each of 98 F2 individuals but only 65 F3 families with enough numbers of F4 seeds for bioassay were obtained. Genotypes of 62 F3 families thus 62 F2individuals for BPH resistance/susceptibility were determined by bioassay of F4 families according to the previously described method (Murata et al. 1998). The heterozygous F3s had 70-75 % resistant F4 progenies, agreeing with that Bph9 was dominant. The segregation ratio in 62 F2s was 12 RR:33 RS:17 SS, which did not deviate from the expected single gene control of resistance. &lt;br /&gt;
&lt;br /&gt;
DNA was extracted from an equal amount (8 g) of leaves of 10 F3 plants derived from each F2 individual. DNA bulks were further prepared by combining four F3 families (each with 10 F3 plants) with RR and SS genotypes, respectively. A total of 106 RFLP markers and eight restriction enzymes were used for the bulked segregant analysis. In addition, a total of 240 random 10-mer primers (Operon Technologies) were surveyed in RAPD-PCR analysis.&lt;br /&gt;
&lt;br /&gt;
Segregation of seven RFLP and two RAPD markers in the 62 F2 plants did not deviate from the expected 1:2:1 ratio or 1:3 ratio. The result indicated no apparent segregation distortion in the chromosomal region covering the Bph9 locus, despite the observed high sterility in this cross combination. Recombination values were calculated by MAPMAKER Version 2.0 with LOD scores greater than 3.0. These markers and Bph9 were located in the 53 cM segment, which was delimited by two RFLP markers (R617 and 1709) on the long arm of chromosome 12 (Fig. 1). A RAPD marker (OPR04) was found to be closest, with a map distance of 8.8 cM from the Bph9 locus. The map distance between the two RFLP markers (G2140 and S2545), however, was much greater than the corresponding distance on the standard Nipponbare/Kasalath map. This might be ascribed either to the use of different mapping populations or to the smaller population size and high sterility in the present cross.&lt;br /&gt;
&lt;br /&gt;
== 【Map position】 ==&lt;br /&gt;
&lt;br /&gt;
[[File:QQ图片20140608222722.jpg]]&lt;br /&gt;
&lt;br /&gt;
== 【Reference】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål, in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181709</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181709"/>
				<updated>2014-06-09T04:07:55Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* 【The discovery of Bph9 map position】 */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
== 【Background】 ==&lt;br /&gt;
&lt;br /&gt;
Genetic and breeding research on the natural resistance system against a serious insect pest of rice, brown planthopper (BPH), Nilaparvata lugens Stal, begun in the mid-1960s. Twelve BPH resistance genes have so far been identified. A BPH resistance gene, Bph10, from Oryza australiensis was first assigned to rice chromosome 12 (Ishii et al. 1994). Later, Bph1from an Indian variety, Mudgo, and bph2 from an IRRI breeding line, IR1154-243, were also mapped on chromosome 12 (Hirabayashi and Ogawa 1995; Murata et al. 1997, 1998).Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000).&lt;br /&gt;
&lt;br /&gt;
== &lt;br /&gt;
==【The discovery of Bph9 map position】 ==&lt;br /&gt;
&lt;br /&gt;
Pokkali, because Norin-PL9 was known to be cross-compatible with indica varieties. Contrary to the expectation, however, this japonica-indica cross resulted in highly sterile F1s and F2s. Ten F3 plants were grown from each of 98 F2 individuals but only 65 F3 families with enough numbers of F4 seeds for bioassay were obtained. Genotypes of 62 F3 families thus 62 F2individuals for BPH resistance/susceptibility were determined by bioassay of F4 families according to the previously described method (Murata et al. 1998). The heterozygous F3s had 70-75 % resistant F4 progenies, agreeing with that Bph9 was dominant. The segregation ratio in 62 F2s was 12 RR:33 RS:17 SS, which did not deviate from the expected single gene control of resistance. &lt;br /&gt;
&lt;br /&gt;
DNA was extracted from an equal amount (8 g) of leaves of 10 F3 plants derived from each F2 individual. DNA bulks were further prepared by combining four F3 families (each with 10 F3 plants) with RR and SS genotypes, respectively. A total of 106 RFLP markers and eight restriction enzymes were used for the bulked segregant analysis. In addition, a total of 240 random 10-mer primers (Operon Technologies) were surveyed in RAPD-PCR analysis.&lt;br /&gt;
&lt;br /&gt;
Segregation of seven RFLP and two RAPD markers in the 62 F2 plants did not deviate from the expected 1:2:1 ratio or 1:3 ratio. The result indicated no apparent segregation distortion in the chromosomal region covering the Bph9 locus, despite the observed high sterility in this cross combination. Recombination values were calculated by MAPMAKER Version 2.0 with LOD scores greater than 3.0. These markers and Bph9 were located in the 53 cM segment, which was delimited by two RFLP markers (R617 and 1709) on the long arm of chromosome 12 (Fig. 1). A RAPD marker (OPR04) was found to be closest, with a map distance of 8.8 cM from the Bph9 locus. The map distance between the two RFLP markers (G2140 and S2545), however, was much greater than the corresponding distance on the standard Nipponbare/Kasalath map. This might be ascribed either to the use of different mapping populations or to the smaller population size and high sterility in the present cross.&lt;br /&gt;
&lt;br /&gt;
== 【Map position】 ==&lt;br /&gt;
&lt;br /&gt;
[[File:QQ图片20140608222722.jpg]]&lt;br /&gt;
&lt;br /&gt;
== 【Reference】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål, in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181708</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181708"/>
				<updated>2014-06-09T04:07:41Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* Background */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
== 【Background】 ==&lt;br /&gt;
&lt;br /&gt;
Genetic and breeding research on the natural resistance system against a serious insect pest of rice, brown planthopper (BPH), Nilaparvata lugens Stal, begun in the mid-1960s. Twelve BPH resistance genes have so far been identified. A BPH resistance gene, Bph10, from Oryza australiensis was first assigned to rice chromosome 12 (Ishii et al. 1994). Later, Bph1from an Indian variety, Mudgo, and bph2 from an IRRI breeding line, IR1154-243, were also mapped on chromosome 12 (Hirabayashi and Ogawa 1995; Murata et al. 1997, 1998).Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000).&lt;br /&gt;
&lt;br /&gt;
== &lt;br /&gt;
==【The discovery of Bph9 map position】 ==&lt;br /&gt;
 ==&lt;br /&gt;
Pokkali, because Norin-PL9 was known to be cross-compatible with indica varieties. Contrary to the expectation, however, this japonica-indica cross resulted in highly sterile F1s and F2s. Ten F3 plants were grown from each of 98 F2 individuals but only 65 F3 families with enough numbers of F4 seeds for bioassay were obtained. Genotypes of 62 F3 families thus 62 F2individuals for BPH resistance/susceptibility were determined by bioassay of F4 families according to the previously described method (Murata et al. 1998). The heterozygous F3s had 70-75 % resistant F4 progenies, agreeing with that Bph9 was dominant. The segregation ratio in 62 F2s was 12 RR:33 RS:17 SS, which did not deviate from the expected single gene control of resistance. &lt;br /&gt;
&lt;br /&gt;
DNA was extracted from an equal amount (8 g) of leaves of 10 F3 plants derived from each F2 individual. DNA bulks were further prepared by combining four F3 families (each with 10 F3 plants) with RR and SS genotypes, respectively. A total of 106 RFLP markers and eight restriction enzymes were used for the bulked segregant analysis. In addition, a total of 240 random 10-mer primers (Operon Technologies) were surveyed in RAPD-PCR analysis.&lt;br /&gt;
&lt;br /&gt;
Segregation of seven RFLP and two RAPD markers in the 62 F2 plants did not deviate from the expected 1:2:1 ratio or 1:3 ratio. The result indicated no apparent segregation distortion in the chromosomal region covering the Bph9 locus, despite the observed high sterility in this cross combination. Recombination values were calculated by MAPMAKER Version 2.0 with LOD scores greater than 3.0. These markers and Bph9 were located in the 53 cM segment, which was delimited by two RFLP markers (R617 and 1709) on the long arm of chromosome 12 (Fig. 1). A RAPD marker (OPR04) was found to be closest, with a map distance of 8.8 cM from the Bph9 locus. The map distance between the two RFLP markers (G2140 and S2545), however, was much greater than the corresponding distance on the standard Nipponbare/Kasalath map. This might be ascribed either to the use of different mapping populations or to the smaller population size and high sterility in the present cross.&lt;br /&gt;
&lt;br /&gt;
== 【Map position】 ==&lt;br /&gt;
&lt;br /&gt;
[[File:QQ图片20140608222722.jpg]]&lt;br /&gt;
&lt;br /&gt;
== 【Reference】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål, in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181703</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181703"/>
				<updated>2014-06-09T04:05:41Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* 【Functions】 */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
== Background ==&lt;br /&gt;
&lt;br /&gt;
Genetic and breeding research on the natural resistance system against a serious insect pest of rice, brown planthopper (BPH), Nilaparvata lugens Stal, begun in the mid-1960s. Twelve BPH resistance genes have so far been identified. A BPH resistance gene, Bph10, from Oryza australiensis was first assigned to rice chromosome 12 (Ishii et al. 1994). Later, Bph1from an Indian variety, Mudgo, and bph2 from an IRRI breeding line, IR1154-243, were also mapped on chromosome 12 (Hirabayashi and Ogawa 1995; Murata et al. 1997, 1998).Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000).&lt;br /&gt;
&lt;br /&gt;
== 【Map position】 ==&lt;br /&gt;
&lt;br /&gt;
[[File:QQ图片20140608222722.jpg]]&lt;br /&gt;
&lt;br /&gt;
== 【Reference】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål, in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181693</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181693"/>
				<updated>2014-06-09T03:37:27Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* Map position */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
== 【Functions】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000).&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== 【Map position】 ==&lt;br /&gt;
&lt;br /&gt;
[[File:QQ图片20140608222722.jpg]]&lt;br /&gt;
&lt;br /&gt;
== 【Reference】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål, in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181691</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181691"/>
				<updated>2014-06-09T03:34:18Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* Map position */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
== 【Functions】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000).&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Map position ==&lt;br /&gt;
&lt;br /&gt;
[[File:QQ图片20140608222722.jpg]]&lt;br /&gt;
&lt;br /&gt;
== 【Reference】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål, in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181690</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181690"/>
				<updated>2014-06-09T03:33:53Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* Map position */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
== 【Functions】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000).&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Map position ==&lt;br /&gt;
&lt;br /&gt;
[File:QQ图片20140608222722.jpg]&lt;br /&gt;
&lt;br /&gt;
== 【Reference】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål, in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:QQ%E5%9B%BE%E7%89%8720140608222722.jpg&amp;diff=181687</id>
		<title>File:QQ图片20140608222722.jpg</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=File:QQ%E5%9B%BE%E7%89%8720140608222722.jpg&amp;diff=181687"/>
				<updated>2014-06-09T03:32:48Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: uploaded a new version of &amp;amp;quot;File:QQ图片20140608222722.jpg&amp;amp;quot;&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181683</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181683"/>
				<updated>2014-06-09T03:28:46Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* 【Functions】 */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
== 【Functions】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000).&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Map position ==&lt;br /&gt;
&lt;br /&gt;
[[File:Example.jpg]]&lt;br /&gt;
&lt;br /&gt;
== 【Reference】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål, in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181659</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181659"/>
				<updated>2014-06-09T03:13:11Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /*  */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
== 【Functions】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000). &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== 【Reference】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål, in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181657</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181657"/>
				<updated>2014-06-09T03:12:41Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /*  */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
== 【Functions】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000). &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== == &lt;br /&gt;
'''【Reference】''' &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål, in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181653</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181653"/>
				<updated>2014-06-09T03:12:03Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /*  */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
== 【Functions】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000). &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== == &lt;br /&gt;
【Reference】 &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål, in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181651</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181651"/>
				<updated>2014-06-09T03:11:46Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: /* 【Functions】 */&lt;/p&gt;
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== 【Functions】 ==&lt;br /&gt;
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Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000). &lt;br /&gt;
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== == &lt;br /&gt;
【Reference】 == ==&lt;br /&gt;
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1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål, in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181649</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181649"/>
				<updated>2014-06-09T03:11:31Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
== 【Functions】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000). &lt;br /&gt;
&lt;br /&gt;
== &lt;br /&gt;
【Reference】 ==&lt;br /&gt;
&lt;br /&gt;
1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål, in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181647</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181647"/>
				<updated>2014-06-09T03:10:49Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
== 【Functions】 ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000). &lt;br /&gt;
&lt;br /&gt;
== &lt;br /&gt;
Reference ==&lt;br /&gt;
&lt;br /&gt;
1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål, in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181641</id>
		<title>Bph9</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=Bph9&amp;diff=181641"/>
				<updated>2014-06-09T03:09:07Z</updated>
		
		<summary type="html">&lt;p&gt;Liye: Created page with &amp;quot;Functions Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (N...&amp;quot;&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Functions&lt;br /&gt;
Bph9, is a dominant brown planthopper resistance gene, locating on the long arm of rice chromosome 12. Bph9 was first identified in a Sri Lankan variety by Nemoto (Nemoto et al. 1989). Then map position of BPH turned out to be on the long arm of rice chromosome 12, which is discovered by Murata in 2000 ( Murata et al. 2000). &lt;br /&gt;
Expression&lt;br /&gt;
Reference&lt;br /&gt;
1.	K. MURATA, M. FUJIWARA, H. MURAI, S. TAKUMI, N. MORI and C. NAKAMURA. Bph9, a dominant brown planthopper resistance gene, is located on the long arm of rice chromosome 12, Rice Genetics Newsletters, 2000, 17(0): 84-86&lt;br /&gt;
2.	Hiroshi Nemoto, Ryoichi Ikeda and Chukichi Kaneda, New genes for resistance to brown planthopper, Nilaparvata lugens Stål, in rice.  Japanese Journal of Breeding, 1989, 39(0): 23-28&lt;/div&gt;</summary>
		<author><name>Liye</name></author>	</entry>

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