节点文献

新疆盐生植物猪毛菜逆向运输蛋白基因SaNHX1 3’-RACE的克隆及序列分析

Clone and Sequence Analysis of 3’RACE of Antiporter Protein Gene SaNHX1 in Xinjiang Halophytes Plant Salsola collina Pall.

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 张雨良罗淑萍杨峰山魏岩袁辉郭长奎

【Author】 ZHANG Yu-liang1,LUO Shu-ping1,YANG Feng-shan2,WEI Yan1,YUAN Hui1,GUO Chang-kui1(1.College of Agronomy,Xinjiang Agricultural University ,Urumqi 830052,China;2.College of Life Science Department,Heilongjiang University,Harbin 150080,China)

【机构】 新疆农业大学黑龙江大学生命科学学院新疆农业大学 乌鲁木齐830052乌鲁木齐830052哈尔滨150080

【摘要】 以新疆盐生植物猪毛菜(Salsola collina Pall.)为材料提取总RNA,根据NHX1家族同源序列保守区设计1对简并引物,进行RT-PCR扩增,得到猪毛菜逆向运输蛋白基因cDNA中间一段619 bp序列。再用快速扩增cDNA 3’末端(3’RACE)方法,得到约1 000 bp 3’末端序列。将两段序列进行拼接,得到猪毛菜长为1 585bp(Gen Bank登陆号为EU072932)的逆向运输蛋白基因(SaNHX1)cDNA序列,编码370个氨基酸,其编码序列、氨基酸序列与同科耐盐植物盐角草相应序列同源性为85%和87%,研究为进一步克隆猪毛菜NHX1全基因序列和研究其功能打下基础。

【Abstract】 Total RNA in this experiment was extracted from Xinjiang halophytes plant Salsola affinis(Salsola collina Pall.).According to NHX1 family homologous sequence conservative region,.one pair of degenerate primers was used for RT-PCR amplification.The results showed that a partial middle 619 bp fragment of SaNHX1 antiporter protein was obtained.The 3’ end sequence was obtained by 3’ RACE method.These two fragments were overlapped,getting SaNHX1 3’terminal fragment 1 585 bp sequence encoding 370 amino acid residues.The codon sequence and amino acid sequence of the 3’ends of SaNHX1 gene were shared by 85% and 87% identity with those of the same family halophytes SeNHX1 gene respectively.This research provided a basic foundation to clone the whole NHX1 sequence and study its structure and function.

【基金】 国家自然科学基金项目(30660033);新疆高校创新研究群体基金项目(XJEDU2004G07)
  • 【文献出处】 新疆农业科学 ,Xinjiang Agricultural Sciences , 编辑部邮箱 ,2008年03期
  • 【分类号】Q943.2
  • 【被引频次】11
  • 【下载频次】423
节点文献中: 

本文链接的文献网络图示:

本文的引文网络