Os01g0580500 - Revision history

Guangyi at 09:38, 19 August 2016

2016-08-19T09:38:51Z

Guangyi: /* Function */

2016-08-19T09:35:17Z

‎Function

Guangyi: /* Annotated Information */

2016-08-19T09:33:55Z

‎Annotated Information

Guangyi: /* Expression */

2016-08-19T09:17:39Z

‎Expression

Guangyi: /* Function */

2016-08-19T09:12:57Z

‎Function

Guangyi at 09:11, 19 August 2016

2016-08-19T09:11:36Z

Guangyi: /* Function */

2016-08-19T09:11:01Z

‎Function

Guangyi: /* Expression */

2016-08-19T09:02:46Z

‎Expression

Guangyi: /* Function */

2016-08-19T08:54:51Z

‎Function

Guangyi: /* References */

2016-08-08T09:41:40Z

‎References

@@ Line 10: / Line 10: @@
 ===Expression===
-Compared with control plants, which include wild-type IL7 and transgenic IL7 lines expressing only an empty vector, ethylene emissions via blast infection during this period were reduced (Fig. 2A) as well as the transcript levels of OsACO5, OsACO7, and OsACS2 (Fig. 2, B and C) in the IRACO10, IRACO101, and IRACS/ACO13 lines.
+*Compared with control plants, which include wild-type IL7 and transgenic IL7 lines expressing only an empty vector, ethylene emissions via blast infection during this period were reduced (Fig. 2A) as well as the transcript levels of OsACO5, OsACO7, and OsACS2 (Fig. 2, B and C) in the IRACO10, IRACO101, and IRACS/ACO13 lines.
 [[File:17-f2.png |center |thumb |10000px |''''''Figure 2. Breakdown of Pi-i-originated blast resistance in ACO/ACS knockdown rice plants. A,Ethylene emission from leaves. Ethylene concentrations emitted from leaves at 36 to 60 hpi were
 normalized with the amount of fungal DNA extracted from the inoculated leaves at 60 hpi.B and C, Relative transcript levels of OsACO5 (B),OsACO7 (B), and OsACS2 (C) genes in leaves at 48 hpi, which were normalized with fungal DNA levels. For A to C, the values are means 6 SE(n = 12). D, Distinct lesion types were apparent in leaves at 8 dpi. Numbers of ELs with an area

@@ Line 5: / Line 5: @@
 *ACO and/or ACS knockdown IL7 rice lines to reveal that HRassociated cyanide/ethylene biosynthesis is required for the resistance to blast fungus.
 *The HR-inducible rice ACS and ACO genes, OsACS2, OsACO5, and OsACO7 (Iwai et al., 2006), were silenced in IL7 line using inverted repeat (IR) constructs that included portions of the corresponding cDNAs (Fig. 1A).
-[[File:17-f1.png |center |thumb |10000px |'''''']]
+[[File:17-f1.png |center |thumb |10000px |''''''Figure 1. Generation of ACO- and ACS/ACO-silenced plants. A, Structure of the OsACS2, OsACO5, and OsACO7 genes and schematic representation of the constructs used to transform rice plants. Boxes below individual cDNAs indicate the regions used for construction. B, Emission of ethylene from leaves after wounding.
 <br>

@@ Line 10: / Line 10: @@
 ===Expression===
 Compared with control plants, which include wild-type IL7 and transgenic IL7 lines expressing only an empty vector, ethylene emissions via blast infection during this period were reduced (Fig. 2A) as well as the transcript levels of OsACO5, OsACO7, and OsACS2 (Fig. 2, B and C) in the IRACO10, IRACO101, and IRACS/ACO13 lines.
-[[File:17-f2.png |center |thumb |10000px |'''''']]
+[[File:17-f2.png |center |thumb |10000px |''''''Figure 2. Breakdown of Pi-i-originated blast resistance in ACO/ACS knockdown rice plants. A,Ethylene emission from leaves. Ethylene concentrations emitted from leaves at 36 to 60 hpi were
+normalized with the amount of fungal DNA extracted from the inoculated leaves at 60 hpi.B and C, Relative transcript levels of OsACO5 (B),OsACO7 (B), and OsACS2 (C) genes in leaves at 48 hpi, which were normalized with fungal DNA levels. For A to C, the values are means 6 SE(n = 12). D, Distinct lesion types were apparent in leaves at 8 dpi. Numbers of ELs with an area
-===Evolution===
+greater than 0.5 mm2 per leaf and their mean areas were determined using 11 leaves for wild-type(WT) Nipponbare, 30 leaves for wild-type IL7, 12 leaves for IRACO10, 19 leaves for IRACO101, and three leaves for IRACS/ACO13. Values given are means 6 SE. One leaf per plant was used. White arrowheads indicate typical ELs in whitish brown.E, Phenotypes of ACO-silenced and control IL7 plants grown in a greenhouse. Left, 50 dpi; right, 70 dpi. For A to E, similar results to wild-type IL7 were obtained by transgenic IL7 plants transformed with the vector alone.'''''']]
-Please input evolution information here.
+<br>
 ==Labs working on this gene==

@@ Line 10: / Line 10: @@
 ===Expression===
 Compared with control plants, which include wild-type IL7 and transgenic IL7 lines expressing only an empty vector, ethylene emissions via blast infection during this period were reduced (Fig. 2A) as well as the transcript levels of OsACO5, OsACO7, and OsACS2 (Fig. 2, B and C) in the IRACO10, IRACO101, and IRACS/ACO13 lines.
 ===Evolution===

@@ Line 5: / Line 5: @@
 *ACO and/or ACS knockdown IL7 rice lines to reveal that HRassociated cyanide/ethylene biosynthesis is required for the resistance to blast fungus.
 *The HR-inducible rice ACS and ACO genes, OsACS2, OsACO5, and OsACO7 (Iwai et al., 2006), were silenced in IL7 line using inverted repeat (IR) constructs that included portions of the corresponding cDNAs (Fig. 1A).
 ===Expression===

← Older revision		Revision as of 09:11, 19 August 2016
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−	~~Please input one-sentence summary here~~.	+	*ACO and/or ACS knockdown IL7 rice lines to reveal that HRassociated cyanide/ethylene biosynthesis is required for the resistance to blast fungus..

	==Annotated Information==		==Annotated Information==

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 ==Annotated Information==
 ===Function===
-Please input function information here.
+The HR-inducible rice ACS and ACO genes, OsACS2, OsACO5, and OsACO7 (Iwai et al., 2006), were silenced in IL7 line using inverted repeat (IR) constructs that included portions of the corresponding cDNAs (Fig. 1A).
 ===Expression===

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 ==References==
-Please input cited references here.
+*'''Bleecker AB, Kende H'''(2000) Ethylene: a gaseous signal molecule in plants. Annu Rev Cell Dev Biol 16: 1–18
 ==Structured Information==
       [[Category:Genes]][[Category:Oryza Sativa Japonica Group]][[Category:Japonica Chromosome 1]]