Os05g0429900 - Revision history

192.168.72.52: /* Structured Information */

2015-06-12T07:39:05Z

‎Structured Information

Zhangamanda: /* References */

2014-05-25T07:19:49Z

‎References

Zhangamanda: /* Labs working on this gene */

2014-05-25T07:16:59Z

‎Labs working on this gene

Zhangamanda: /* Expression */

2014-05-25T07:16:07Z

‎Expression

Zhangamanda: /* Function */

2014-05-25T07:11:41Z

‎Function

Zhangamanda: /* Labs working on this gene */

2014-05-25T06:37:50Z

‎Labs working on this gene

Zhangamanda: /* Expression */

2014-05-25T06:37:21Z

‎Expression

Zhangamanda: /* Function */

2014-05-25T06:36:59Z

‎Function

Zhangamanda: /* Expression */

2014-05-25T02:53:37Z

‎Expression

Zhangamanda: /* Function */

2014-05-25T02:50:13Z

‎Function

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 ==Structured Information==
 [[Category:Genes]]
 [[Category:Japonica mRNA]]

@@ Line 19: / Line 19: @@
 ==References==
-Chang-Jie Jiang,1 Masaki Shimono,1 Satoru Maeda,1 Haruhiko Inoue,1 Masaki Mori,1Morifumi Hasegawa,2 Shoji Sugano,1 and Hiroshi Takatsuji1.Suppression of the Rice Fatty-Acid Desaturase Gene OsSSI2 Enhances Resistance to Blast and Leaf Blight Diseases in Rice.MPMI 2009,22(7): 820–829.
+Xianwen Zhang , Wirat Rerksiri, Ailing Liu , Xiaoyun Zhou , Hairong Xiong , Jianhua Xiang ,Xinbo Chen , Xingyao Xiong.Transcriptome profile reveals heat response mechanism at molecular and metabolic levels in rice flag leaf.Gene, 2013,530: 185–192.
 ==Structured Information==

← Older revision		Revision as of 07:16, 25 May 2014
Line 14:		Line 14:

	==Labs working on this gene==		==Labs working on this gene==
		+	Key Laboratory for Crop Germplasm Innovation and Utilization of Hunan Province, Hunan Agricultural University, Changsha, China
		+	College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha, China
		+	Center of Analysis and Testing, Hunan Agricultural University, Changsha, China

	==References==		==References==

← Older revision		Revision as of 07:16, 25 May 2014
Line 6:		Line 6:

	===Expression===		===Expression===
		+	MYBS3 activated cold signaling pathway in rice. Some research showed that, among 27 HR Myb genes, 17 genes were early activated, two (Os02g0624300 and Os05g0429900)were continuously up-regulated.

	===Evolution===		===Evolution===

@@ Line 3: / Line 3: @@
 ==Annotated Information==
 ===Function===
 ===Expression===

← Older revision		Revision as of 06:37, 25 May 2014
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	==Labs working on this gene==		==Labs working on this gene==
−	~~Plant Disease Resistance Research Unit, Division of Plant Science, National Institute of Agrobiological Sciences,~~
−	~~Kannondai , Tsukuba, 305-8602 Japan; College of Agriculture, Ibaraki University, Ami 300-0393, Japan~~
−
−	~~Shanghai Agrobiological Gene Center, Shanghai, P. R. China~~
−	~~CAS Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese~~
−	~~cademy of Sciences, Dalian, P. R. China~~
−	~~National Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University, Wuhan, P. R. China~~

	==References==		==References==

← Older revision		Revision as of 06:37, 25 May 2014
Line 5:		Line 5:

	===Expression===		===Expression===
−	A genomic database search revealed that the rice genome encodes seven SACPD-like proteins that have 46 to 86% amino acid sequence identity with Arabidopsis SSI2Prediction of subcellular targeting by using the TargetP and WoLF PSORT prediction programs suggested that Os01g0919900,Os01g0880800, and Os08g0199400 are localized in the chloplast or mitochondrion, whereas the others are present in chloroplasts.These predictions are consistent with findings that FA synthesis in plants occurs mainly in plastids .
−	~~[[File:zxq1.png\|200px\|thumb\|left\|Fig. 1. RNA blot analysis.]]~~
−
−
−	Fig:Transcripts of OsSSI2, two OsSSI2 homologs,WRKY45, and PR1b were analyzed in wild-type (WT) and OsSSI2 mutant plants. OsSSI2 transcripts were not detected in homozygous Osssi2-Tos17 (NF7039) and OsSSI2-knockdown (kd) plants, whereas the expression of the two closest homologs of OsSSI2 (i.e., Os04g0379900 and
−	~~Os01g0880800) was unaffected in these plants. The arrow indicates a band of fusion transcripts encoding OsSSI2 with the Tos17 insertion. The salicylic~~
−	acid/benzothiadiazole-induced gene WRKY45 and the pathogenesis-related gene OsPR1b were constitutively expressed in the NF7039 and OsSSI2-kd plants. Leaf blades from the fourth leaves of seedlings were used.

	===Evolution===		===Evolution===

@@ Line 6: / Line 6: @@
 ===Expression===
-Prediction
+A genomic database search revealed that the rice genome encodes seven SACPD-like proteins that have 46 to 86% amino acid sequence identity with Arabidopsis SSI2Prediction of subcellular targeting by using the TargetP and WoLF PSORT prediction programs suggested that Os01g0919900,Os01g0880800, and Os08g0199400 are localized in the chloplast or mitochondrion, whereas the others are present in chloroplasts.These predictions are consistent with findings that FA synthesis in plants occurs mainly in plastids .
 [[File:zxq1.png|200px|thumb|left|Fig. 1. RNA blot analysis.]]
-Fig:Transcripts of OsSSI2, two OsSSI2 homologs,
+Fig:Transcripts of OsSSI2, two OsSSI2 homologs,WRKY45, and PR1b were analyzed in wild-type (WT) and OsSSI2 mutant plants. OsSSI2 transcripts were not detected in homozygous Osssi2-Tos17 (NF7039) and OsSSI2-knockdown (kd) plants, whereas the expression of the two closest homologs of OsSSI2 (i.e., Os04g0379900 and
-WRKY45, and PR1b were analyzed in wild-type (WT) and OsSSI2 mutant
+Os01g0880800) was unaffected in these plants. The arrow indicates a band of fusion transcripts encoding OsSSI2 with the Tos17 insertion. The salicylic
-plants. OsSSI2 transcripts were not detected in homozygous Osssi2-Tos17
+acid/benzothiadiazole-induced gene WRKY45 and the pathogenesis-related gene OsPR1b were constitutively expressed in the NF7039 and OsSSI2-kd plants. Leaf blades from the fourth leaves of seedlings were used.
 ===Evolution===