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重瓣榆叶梅PrtSHP的基因克隆与序列结构分析
引用本文:刘志雄,于先泥.重瓣榆叶梅PrtSHP的基因克隆与序列结构分析[J].湖北农业科学,2012,51(10):2124-2127.
作者姓名:刘志雄  于先泥
作者单位:长江大学园艺园林学院,湖北荆州,434025
基金项目:国家自然科学基金项目(31101202);长江大学博士启动基金项目
摘    要:采用同源克隆法结合3′-RACE技术从重瓣榆叶梅(Prunus triloba var.Plena)中分离得到了1个雌蕊和果实发育调控基因SHP的同源基因PrtSHP的全长cDNA(GenBank登录号:JF911701).其cDNA全长970 bp,包括1个编码244个氨基酸的735 bp的完整开放阅读框.蛋白质序列比对和分子系统发生分析表明,PrtSHP是拟南芥的SHP的同源基因,其编码的蛋白质的C末端结构域具有2个高度保守的模体(AG Ⅰ模体和AG Ⅱ模体),属C类转录因子中PLE进化系.

关 键 词:重瓣榆叶梅(Prunus  triloba  var.Plena)  雌蕊和果实发育  基因克隆  序列分析

Gene Clone and Sequence Analysis of PrtSHP from Prunus triloba var. Plena
LIU Zhi-xiong , YU Xian-ni.Gene Clone and Sequence Analysis of PrtSHP from Prunus triloba var. Plena[J].Hubei Agricultural Sciences,2012,51(10):2124-2127.
Authors:LIU Zhi-xiong  YU Xian-ni
Affiliation:(College of Horticulture and Gardening,Yangtze University,Jingzhou 434025,Hubei,China)
Abstract:The total cDNA sequence of PrtSHP(GenBank accession code,JF911701) of Prunus triloba var.Plena,the homologous gene of pistil and fruit developmentally regulated gene SHP,was obtained by homology cloning combined with 3′-RACE.The full length of PrtSHP cDNA was 970 bp,including an open reading frame(ORF) of 735 bp which code a polypeptide of 244 amino acids.Sequence comparison and phylogenetic analysis revealed that PrtSHP was highly homologous to protein SHP in Arabidopsis and belonged to the PLE clade of class C.The C-terminal domain of the predicted amino acid sequence of PrtSHP harbored two highly conserved motifs(AG Ⅰand AG Ⅱ).
Keywords:Prunus triloba var  Plena  pistil and fruit development  gene clone  sequence analysis
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