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小麦TaCIPK31基因的克隆及生物信息学分析

韩玲玲 江行玉 李海霞 董中东 陈锋 崔党群 许海霞

河南农业大学学报2013,Vol.47Issue(3):262-267,6.
河南农业大学学报2013,Vol.47Issue(3):262-267,6.

小麦TaCIPK31基因的克隆及生物信息学分析

Full-length cloning and bioinformatics analysis of TaCIPK31 gene in wheat

韩玲玲 1江行玉 2李海霞 1董中东 1陈锋 1崔党群 1许海霞1

作者信息

  • 1. 河南农业大学河南省粮食作物生理生态与遗传改良国家重点实验室培育基地,河南 郑州 450002
  • 2. 海南大学农学院,海南 海口 570228
  • 折叠

摘要

Abstract

Based on the wheat CIPK EST sequence of TC95390,we got the 3'-end and 5'-end using RACE (rapid-amplification of cDNA ends) method from wheat cultivar Shi 4185 which has higherdrought-resistance and salt-resistance.The whole sequence of gene was analyzed and named as TaCIPK31 by sequence homology and deposited in GenBank database of accession number JX625142.1.Bioinformatics analysis was undergone meanwhile.The results showed that the ORF length of TaCIPK31 was 1 350 bp and encoded 449 amino acids.The pI and Mw of TaCIPK31 were 8.27 and 50.9 kD,respectively.TaCIPK31 was a hydrophilic stable protein while there was only one significant hydrophobic peak and one transmembrane peptide.The TaCIPK31 protein contained a catalytic Ser/Thr protein domain in its N-terminal region and a regulatory domain with NAF motif at its C-terminus,which is in line with the typical CIPK structural characteristics.The amino acids sequence analysis showed that TaCIPK31 has higher homology with HvCIPK31,OsCIPK3 and ZmCIPK31.

关键词

小麦/TaCIPK31/cDNA末端快速扩增技术/基因克隆/生物信息学分析

Key words

wheat (Triticum aestivum) / TaCIPK31 / rapid-amplification of cDNA ends / gene clone /bioinformatics analysis

分类

农业科技

引用本文复制引用

韩玲玲,江行玉,李海霞,董中东,陈锋,崔党群,许海霞..小麦TaCIPK31基因的克隆及生物信息学分析[J].河南农业大学学报,2013,47(3):262-267,6.

基金项目

国家自然科学基金项目(31101207 ()

31160185) ()

河南农业大学学报

OA北大核心CSCDCSTPCD

1000-2340

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