Os04g0504000 - Revision history

192.168.72.52: /* Structured Information */

2015-06-12T07:07:05Z

‎Structured Information

Liuxianju: /* Expression */

2014-06-07T08:02:00Z

‎Expression

Liuxianju: /* Function */

2014-06-07T08:00:38Z

‎Function

Liuxianju: /* Evolution */

2014-06-07T07:55:53Z

‎Evolution

Liuxianju: /* References */

2014-06-07T07:52:51Z

‎References

Liuxianju: /* Structured Information */

2014-06-07T07:52:22Z

‎Structured Information

Penny: /* References */

2014-06-07T07:47:48Z

‎References

Penny: /* References */

2014-06-07T07:47:04Z

‎References

Penny: /* Labs working on this gene */

2014-06-07T07:38:05Z

‎Labs working on this gene

Penny: /* Expression */

2014-06-07T07:32:35Z

‎Expression

@@ Line 64: / Line 64: @@
 ==Structured Information==
 [[Category:Genes]]
 [[Category:Japonica mRNA]]

← Older revision		Revision as of 08:02, 7 June 2014
Line 9:		Line 9:

	the gene, ''Os04g0504000'' encodes a putative a putative adenine phosphoribosyl transgerase (APRT). In plants, adenine phosphoribosyl transferase (APRT) is the primary enzyme that converts adenine into adenosine-5'-monophosphate( AMP) in the salvage metabolism pathway. The balance of adenosine triphosphate( ATP) in the cell is maintained by two biosynthetic pathways: ''de novo'' adenine biosynthesis and purine salvage pathway, adenine may be converted to AMP via two possible pathways" a single step pathway involving APRT activity and a two-step pathway involving the sequential action of adenosine phosphorylase and adenosine kinase( ADK). the single step APRT pathway is the predominant pathway for the salvaging of adenine in plants under stress conditions.In contrast to the ''de novo'' purine biosynthetic pathway, purine salvage is more efficient due to its ability to convert adenine, a byproduct of many biochemical reactions, into AMP.The mutant of the gene ''Os04g0504000'' is male sterile due to abortion of pollen development after the meiotic division of the pollen mother cell.and it is likely to be involved in TGMS in the rice line 'Annong S-1'.		the gene, ''Os04g0504000'' encodes a putative a putative adenine phosphoribosyl transgerase (APRT). In plants, adenine phosphoribosyl transferase (APRT) is the primary enzyme that converts adenine into adenosine-5'-monophosphate( AMP) in the salvage metabolism pathway. The balance of adenosine triphosphate( ATP) in the cell is maintained by two biosynthetic pathways: ''de novo'' adenine biosynthesis and purine salvage pathway, adenine may be converted to AMP via two possible pathways" a single step pathway involving APRT activity and a two-step pathway involving the sequential action of adenosine phosphorylase and adenosine kinase( ADK). the single step APRT pathway is the predominant pathway for the salvaging of adenine in plants under stress conditions.In contrast to the ''de novo'' purine biosynthetic pathway, purine salvage is more efficient due to its ability to convert adenine, a byproduct of many biochemical reactions, into AMP.The mutant of the gene ''Os04g0504000'' is male sterile due to abortion of pollen development after the meiotic division of the pollen mother cell.and it is likely to be involved in TGMS in the rice line 'Annong S-1'.
		+	Xa-21 is the first important functions has been cloned from wild rice gene. Khush reported their resistant donor for West Africa long medicine wild rice (Oryza LONGISTAMINATA), in rice late tillering stage anti when Philippines all 6 races. The hybrid IR24 gene by backcross, self access, BC4F2 group, F2 group of two to 1, 2 Philippines, 4 and 6 of the genetics of resistance, showed that the resistance was controlled by a dominant gene, is different from the 17 resistance genes have been identified, named Xa-21, later further breeding with near isogenic line IRBB21 Xa-21. Ronald Xa-21 on the eleventh chromosome, genetic map and RAPD818, RAPD248 and RG103 marker distance not exceeding 1.2cM. Then the gene cloning by Song Wenyuan etc., and widely used in domestic and foreign rice bacterial leaf blight of transgenic breeding

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

@@ Line 4: / Line 4: @@
 ===Function===
 the rice gene, ''Os04g0504000'',or named ''OsAPT2'',contains seven exons and six introns.And it encodes a putative adenine phosphoribosyl transferase( APRT).The deduced amino acid sequence of ''Os04g0504000''is highly homologous to those of previously isolated APRTs.The observed heat-induced change in the ''Os04g0504000''expression pattern in young panicles may mediate, at least in part, thermo-sensitive genic male sterility( TGMS)in 'Annong S-1'.the ''Os04g0504000''is likely to be involved in TGMS in the rice line 'Annong S-1'.
 ===Expression===

← Older revision		Revision as of 07:55, 7 June 2014
Line 13:		Line 13:

	You can also add sub-section(s) at will.		You can also add sub-section(s) at will.
		+	in Chromosomes 11

	==Labs working on this gene==		==Labs working on this gene==

@@ Line 20: / Line 20: @@
 #  Chun-Jiang Zhou, Jun Li and Ji-Cheng Zou.2006.Cloning and characterization of a second form of the rice adenine phosphoribosyl transferase gene (''OsAPT2'') and its association with TGMS.Plant Molecular Biology (2006) 60:365–376
 #  WENG Man-li,WANG Wang and ZHOU Chun-jiang.Cloning and genetic transformation of a novel rice gene OsAPT2.Journal of Hunan Agricultural University (Natural Sciences)(2007)33.
 ==Structured Information==

@@ Line 34: / Line 34: @@
              Spermatophyta; Magnoliophyta; Liliopsida; Poales; Poaceae; BEP
              clade; Ehrhartoideae; Oryzeae; Oryza.
+. 闫成业;刘艳;牟同敏
 Chromosome = [[:category:Japonica Chromosome 4|Chromosome 4]]|
 AP = Chromosome 4:25564488..25569281|

@@ Line 18: / Line 18: @@
 ==References==
-# one Chun-Jiang Zhou, Jun Li and Ji-Cheng Zou.2006.Cloning and characterization of a second form of the rice adenine phosphoribosyl transferase gene (''OsAPT2'') and its association with TGMS.Plant Molecular Biology (2006) 60:365–376
+#  Chun-Jiang Zhou, Jun Li and Ji-Cheng Zou.2006.Cloning and characterization of a second form of the rice adenine phosphoribosyl transferase gene (''OsAPT2'') and its association with TGMS.Plant Molecular Biology (2006) 60:365–376
-# two WENG Man-li,WANG Wang and ZHOU Chun-jiang.Cloning and genetic transformation of a novel rice gene OsAPT2.Journal of Hunan Agricultural University (Natural Sciences)(2007)33.
+#  WENG Man-li,WANG Wang and ZHOU Chun-jiang.Cloning and genetic transformation of a novel rice gene OsAPT2.Journal of Hunan Agricultural University (Natural Sciences)(2007)33.
 ==Structured Information==

@@ Line 15: / Line 15: @@
 ==Labs working on this gene==
-Please input related labs here.
+The State Key Laboratory of Plant Genomics,Institute of Genetics and Developmental Biology,CAS.
 ==References==

@@ Line 6: / Line 6: @@
 ===Expression===
-Please input expression information here.
 ===Evolution===