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‘津田’芜菁Transparent Testa Glabra 1(BrTTG1)基因的克隆及表达分析
引用本文:闫海芳,李玉花,刘振华,闵远琴.‘津田’芜菁Transparent Testa Glabra 1(BrTTG1)基因的克隆及表达分析[J].植物生理学通讯,2011(4):373-378.
作者姓名:闫海芳  李玉花  刘振华  闵远琴
作者单位:东北林业大学生命科学学院;
基金项目:国家自然科学基金重点项目(30730078); 中央高校基本科研业务费专项资金(DL09BA09)
摘    要:TTG1(Transparent Testa Glabra 1)蛋白是一种WD40类蛋白,参与植物的生长和发育。采用RT-PCR方法从芜菁品种‘津田'中克隆了BrTTG1 cDNA序列(GenBank登录号HM208590)。该基因cDNA开放阅读框长度为1 014 bp,编码一个由337个氨基酸残基组成的蛋白,该蛋白分子量为37.28 kDa,理论等电点为4.66。与其他植物中的TTG1蛋白进行同源性比对结果显示,BrTTG1与甘蓝型油菜的TTG1同源性最高。BrTTG1蛋白在31~337位氨基酸处含有WD40超家族的保守结构域。荧光定量PCR检测BrTTG1在‘津田'芜菁不同组织中的表达结果表明,该基因在有花青素合成的红色‘津田'芜菁根皮中表达量最高。

关 键 词:‘津田’芜菁  TTG1  基因克隆  表达分析

Cloning and Expression Analysis of Transparent Testa Glabra 1(BrTTG1) in Brassica rapa L.cv.'Tsuda'
YAN Hai-Fang,LI Yu-Hua,LIU Zhen-Hua,MIN Yuan-Qin College of Life Sciences,Northeast Forestry University,Harbin ,China.Cloning and Expression Analysis of Transparent Testa Glabra 1(BrTTG1) in Brassica rapa L.cv.'Tsuda'[J].Plant Physiology Communications,2011(4):373-378.
Authors:YAN Hai-Fang  LI Yu-Hua  LIU Zhen-Hua  MIN Yuan-Qin College of Life Sciences  Northeast Forestry University  Harbin  China
Institution:YAN Hai-Fang,LI Yu-Hua~*,LIU Zhen-Hua,MIN Yuan-Qin College of Life Sciences,Northeast Forestry University,Harbin 150040,China
Abstract:TTG1(transparent testa glabra 1) is a WD40 protein that is involved in plant growth and development. Here,a homologue of transparent testa glabra 1 gene,designated BrTTG1,was isolated from 'Tsuda' (Brassica rapa L.) by RT-PCR(GenBank accession number HM208590).The ORF of the BrTTG1 was 1 014 bp long and encoded a putative protein of 337 amino acids with a molecular weight of 37.28 kDa and a theoretical pI of 4.66.BrTTG1 protein contained a WD40 superfamily conserved domain and had a high identity with TTG1 ...
Keywords:Brassica rapa L  cv  'Tsuda'  TTG1  gene cloning  expressing analysis  
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