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		<id>http://192.168.164.12:81/ricewiki/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Yuelvwaer</id>
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		<updated>2026-10-12T05:37:31Z</updated>
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	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=LOC_Os08g30910&amp;diff=175716</id>
		<title>LOC Os08g30910</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=LOC_Os08g30910&amp;diff=175716"/>
				<updated>2014-06-01T14:55:52Z</updated>
		
		<summary type="html">&lt;p&gt;Yuelvwaer: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Introduction：&lt;br /&gt;
&lt;br /&gt;
Histone lysine methylation plays an important role in heterochromatin formation and reprogramming of gene expression. SET-domain-containing proteins are shown to have histone lysine methyltransferase activities. A large number of SET-domain genes are identified in plant genomes. The function of most SET-domain genes is not known. In this work, we studied the 12 rice (Oryza sativa) homologs of Su(var)3–9, the histone H3 lysine 9 (H3K9) methyltransferase identified in Drosophila. Several rice SUVHs (i.e. SDG714, SDG727, and SDG710) were found to have an antagonistic function to the histone H3K9 demethylase JMJ706, as down-regulation of these genes could partially complement the jmj706 phenotype and reduced histone H3K9 methylation. Down-regulation of a rice Su(var)3–9 homolog (SUVH), namely SDG728, decreased H3K9 methylation and altered seed morphology. Overexpression of the gene increased H3K9 methylation. SDG728 and other SUVH genes were found to be involved in the repression of retrotransposons such as Tos17 and a Ty1-copia element. Analysis of histone methylation suggested that SDG728-mediated H3K9 methylation may play an important role in retrotransposon repression.&lt;br /&gt;
&lt;br /&gt;
Gene      	Clone      	Chr	Locn	Hit  	Dir	FromTo   	Type&lt;br /&gt;
______________________________________________________________________________________________&lt;br /&gt;
&lt;br /&gt;
Os08g30910	PFG_3B-00273.L	chr08	W/19082792-19086784	1000-Promotor	C	19081650-19081877	PFG T-DNA&lt;br /&gt;
Os08g30910	GCAGAGCTGTACCGTGC	chr08	W/19082792-19086784	1000-Promotor	W	19081897-19081913	smRNA MPSS&lt;br /&gt;
Os08g30910	CTGTACCGTGCAGGCAC	chr08	W/19082792-19086784	1000-Promotor	W	19081903-19081919	smRNA MPSS&lt;br /&gt;
Os08g30910	smRNA90883_1x	chr08	W/19082792-19086784	1000-Promotor	W	19082129-19082152	smRNA CSRDB&lt;br /&gt;
Os08g30910	AGAAATGGGCTCGAGTT	chr08	W/19082792-19086784	1000-Promotor	C	19082140-19082156	smRNA MPSS&lt;br /&gt;
Os08g30910	CGGCTCGAGTTGGTGCC	chr08	W/19082792-19086784	1000-Promotor	W	19082190-19082206	smRNA MPSS&lt;br /&gt;
Os08g30910	FL039956	chr08	W/19082792-19086784	Exon	C	19085021-19085620	RTIM Tos17&lt;br /&gt;
Os08g30910	RMD_TTosR-04Z11HS51_TosRS	chr08	W/19082792-19086784	Exon	C	19085209-19085359	RMD T-DNA&lt;br /&gt;
Os08g30910	RMD_TTosR-04Z11HT27_TosRS	chr08	W/19082792-19086784	Exon	C	19085216-19085790	RMD T-DNA&lt;br /&gt;
Os08g30910	PFG_4A-00775.R	chr08	W/19082792-19086784	Exon	W	19085272-19086009	PFG T-DNA&lt;br /&gt;
Os08g30910	RMD_04Z11AA68	chr08	W/19082792-19086784	Exon	W	19085355-19085620	RMD T-DNA&lt;br /&gt;
Os08g30910	RMD_TTosL-04Z11AA68_TosRS	chr08	W/19082792-19086784	Exon	W	19085355-19085620	RMD T-DNA&lt;br /&gt;
Os08g30910	BT068011	chr08	W/19082792-19086784	Exon	W	19085819-19086838	Maize cDNA&lt;br /&gt;
Os08g30910	FL047512	chr08	W/19082792-19086784	Exon	C	19086009-19086608	RTIM Tos17&lt;br /&gt;
Os08g30910	FL047532	chr08	W/19082792-19086784	Exon	C	19086009-19086608	RTIM Tos17&lt;br /&gt;
Os08g30910	FL051969	chr08	W/19082792-19086784	Exon	C	19086009-19086608	RTIM Tos17&lt;br /&gt;
Os08g30910	NC0178_0_103_1A	chr08	W/19082792-19086784	Exon	C	19086009-19086521	RTIM Tos17&lt;br /&gt;
Os08g30910	BT055122	chr08	W/19082792-19086784	Exon	W	19086071-19086832	Maize cDNA&lt;br /&gt;
Os08g30910	FL012413	chr08	W/19082792-19086784	Exon	W	19086112-19086502	RTIM Tos17&lt;br /&gt;
Os08g30910	FL049049	chr08	W/19082792-19086784	Exon	W	19086151-19086735	RTIM Tos17&lt;br /&gt;
Os08g30910	NE9001_0_502_1A	chr08	W/19082792-19086784	Exon	C	19086155-19086411	RTIM Tos17&lt;br /&gt;
Os08g30910	BT055367	chr08	W/19082792-19086784	Exon	W	19086176-19086638	Maize cDNA&lt;br /&gt;
Os08g30910	BT068432	chr08	W/19082792-19086784	Exon	W	19086176-19086638	Maize cDNA&lt;br /&gt;
Os08g30910	AY187719	chr08	W/19082792-19086784	Exon	W	19086185-19086562	Maize cDNA&lt;br /&gt;
Os08g30910	At2g23740	chr08	W/19082792-19086784	Exon	W	19086185-19086564	Arabidopsis cDNA&lt;br /&gt;
Os08g30910	At5g43990	chr08	W/19082792-19086784	Exon	W	19086185-19086638	Arabidopsis cDNA&lt;br /&gt;
Os08g30910	EU970110	chr08	W/19082792-19086784	Exon	W	19086191-19086537	Maize cDNA&lt;br /&gt;
Os08g30910	At3g03750	chr08	W/19082792-19086784	Exon	W	19086191-19086537	Arabidopsis cDNA&lt;br /&gt;
Os08g30910	FL049037	chr08	W/19082792-19086784	300-UTR3	C	19086206-19086805	RTIM Tos17&lt;br /&gt;
Os08g30910	EU968739	chr08	W/19082792-19086784	Exon	W	19086317-19086560	Maize cDNA&lt;br /&gt;
Os08g30910	FL048039	chr08	W/19082792-19086784	Exon	W	19086347-19086946	RTIM Tos17&lt;br /&gt;
Os08g30910	FL048371	chr08	W/19082792-19086784	Exon	W	19086347-19086946	RTIM Tos17&lt;br /&gt;
Os08g30910	FL048640	chr08	W/19082792-19086784	Exon	W	19086347-19086946	RTIM Tos17&lt;br /&gt;
Os08g30910	T36759T	chr08	W/19082792-19086784	Exon	W	19086347-19086798	RTIM Tos17&lt;br /&gt;
Os08g30910	T36794T	chr08	W/19082792-19086784	Exon	W	19086347-19086802	RTIM Tos17&lt;br /&gt;
Os08g30910	NE4522_0_502_1A	chr08	W/19082792-19086784	300-UTR3	C	19086386-19087072	RTIM Tos17&lt;br /&gt;
Os08g30910	FL028481	chr08	W/19082792-19086784	Exon	W	19086407-19087006	RTIM Tos17&lt;br /&gt;
Os08g30910	NC2294_0_502_1A	chr08	W/19082792-19086784	300-UTR3	C	19086528-19087036	RTIM Tos17&lt;br /&gt;
Os08g30910	FL039835	chr08	W/19082792-19086784	Exon	W	19086674-19087269	RTIM Tos17&lt;br /&gt;
Os08g30910	FL039883	chr08	W/19082792-19086784	Exon	W	19086674-19087273	RTIM Tos17&lt;br /&gt;
Os08g30910	FL040227	chr08	W/19082792-19086784	Exon	W	19086674-19087273	RTIM Tos17&lt;br /&gt;
Os08g30910	FL040231	chr08	W/19082792-19086784	Exon	W	19086674-19087273	RTIM Tos17&lt;br /&gt;
Os08g30910	FL040245	chr08	W/19082792-19086784	Exon	W	19086674-19087207	RTIM Tos17&lt;br /&gt;
Os08g30910	FL040441	chr08	W/19082792-19086784	Exon	W	19086674-19086918	RTIM Tos17&lt;br /&gt;
Os08g30910	FL040529	chr08	W/19082792-19086784	Exon	W	19086674-19087167	RTIM Tos17&lt;br /&gt;
Os08g30910	FL040652	chr08	W/19082792-19086784	Exon	W	19086674-19087273	RTIM Tos17&lt;br /&gt;
Os08g30910	FL040775	chr08	W/19082792-19086784	Exon	W	19086674-19087273	RTIM Tos17&lt;br /&gt;
Os08g30910	FL041055	chr08	W/19082792-19086784	Exon	W	19086674-19087273	RTIM Tos17&lt;br /&gt;
Os08g30910	FL041071	chr08	W/19082792-19086784	Exon	W	19086674-19087273	RTIM Tos17&lt;br /&gt;
Os08g30910	NF6033_0_401_1A	chr08	W/19082792-19086784	Exon	W	19086674-19087273	RTIM Tos17&lt;br /&gt;
Os08g30910	NF6033_0_405_1A	chr08	W/19082792-19086784	Exon	W	19086674-19087273	RTIM Tos17&lt;br /&gt;
Os08g30910	NF6033_0_501_1A	chr08	W/19082792-19086784	Exon	W	19086674-19087065	RTIM Tos17&lt;br /&gt;
Os08g30910	NF6817_0_404_1A	chr08	W/19082792-19086784	Exon	W	19086674-19087217	RTIM Tos17&lt;br /&gt;
Os08g30910	FL019847	chr08	W/19082792-19086784	300-UTR3	W	19086878-19087171	RTIM Tos17&lt;br /&gt;
Os08g30910	FL019972	chr08	W/19082792-19086784	300-UTR3	W	19086878-19087477	RTIM Tos17&lt;br /&gt;
Os08g30910	FL021193	chr08	W/19082792-19086784	300-UTR3	W	19086878-19087479	RTIM Tos17&lt;/div&gt;</summary>
		<author><name>Yuelvwaer</name></author>	</entry>

	<entry>
		<id>https://ngdc.cncb.ac.cn/ricewiki/index.php?title=LOC_Os08g30910&amp;diff=173716</id>
		<title>LOC Os08g30910</title>
		<link rel="alternate" type="text/html" href="https://ngdc.cncb.ac.cn/ricewiki/index.php?title=LOC_Os08g30910&amp;diff=173716"/>
				<updated>2014-05-28T15:54:31Z</updated>
		
		<summary type="html">&lt;p&gt;Yuelvwaer: Created page with &amp;quot;Plant histone methyltransferases; SET domain; demethylases; DNA methylation; retrotransposon; epigenetic modification; rice chromatin Histone lysine methylation plays an impor...&amp;quot;&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Plant histone methyltransferases; SET domain; demethylases; DNA methylation; retrotransposon; epigenetic modification; rice chromatin&lt;br /&gt;
Histone lysine methylation plays an important role in heterochromatin formation and reprogramming of gene expression. SET-domain-containing proteins are shown to have histone lysine methyltransferase activities. A large number of SET-domain genes are identified in plant genomes. The function of most SET-domain genes is not known. In this work, we studied the 12 rice (Oryza sativa) homologs of Su(var)3–9, the histone H3 lysine 9 (H3K9) methyltransferase identified in Drosophila. Several rice SUVHs (i.e. SDG714, SDG727, and SDG710) were found to have an antagonistic function to the histone H3K9 demethylase JMJ706, as down-regulation of these genes could partially complement the jmj706 phenotype and reduced histone H3K9 methylation. Down-regulation of a rice Su(var)3–9 homolog (SUVH), namely SDG728, decreased H3K9 methylation and altered seed morphology. Overexpression of the gene increased H3K9 methylation. SDG728 and other SUVH genes were found to be involved in the repression of retrotransposons such as Tos17 and a Ty1-copia element. Analysis of histone methylation suggested that SDG728-mediated H3K9 methylation may play an important role in retrotransposon repression.&lt;/div&gt;</summary>
		<author><name>Yuelvwaer</name></author>	</entry>

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