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新牧1号苜蓿MvDREB基因的克隆和序列分析
引用本文:帕尔哈提·阿布都克日木,许磊,朱超,努尔凯麦尔·木拉提,张桦.新牧1号苜蓿MvDREB基因的克隆和序列分析[J].喀什师范学院学报,2014(3):20-23.
作者姓名:帕尔哈提·阿布都克日木  许磊  朱超  努尔凯麦尔·木拉提  张桦
作者单位:[1]新疆农业大学农学院,乌鲁木齐830052 [2]喀什师范学院生物与地理科学系,新疆喀什844008
基金项目:新疆高技术研究发展项目(201211105)
摘    要:以新牧1号苜蓿为研究材料,采用RT-PCR方法,设计特异引物,从新牧1号苜蓿中克隆获得MvDREB基因cDNA,测序结果该片段全长为651 bp,Genbank登录号为GU073286.生物信息学分析结果表明,该基因序列与紫花苜蓿核苷酸序列相似度达99%,编码216个氨基酸,MvDREB蛋白氨基酸序列分析比对显示该蛋白属于AP2/ERF家族的亲水性核蛋白,蛋白质分子量为24873.1,理论等电点pI为5.90,不稳定参数为45.07.

关 键 词:新牧1号苜蓿  MvDREB  序列分析

Cloning and Sequence Analysis of MvDREB Gene in Medicago Varia Xinmu No.1
Paerhati Abudukerimu,XU Lei,ZHU Chao,Nuerkaimaier Mulati,ZHANG Hua.Cloning and Sequence Analysis of MvDREB Gene in Medicago Varia Xinmu No.1[J].Journal of Kashgar Teachers College,2014(3):20-23.
Authors:Paerhati Abudukerimu  XU Lei  ZHU Chao  Nuerkaimaier Mulati  ZHANG Hua
Institution:1.College of agriculture, Xinjiang Agricultural University, Urumqi 830052,Xinjiang, China; 2. Departement of Biologic and Geographic Scienees,Kashgar Teachers Cortege, Kashgar 844008,Xinjing, China )
Abstract:Using RT-PCR method and designing specific primers, we cloned the cDNA of MvDREB gene in Med-icago.varia.xinmu No.1. the MvDREB(GU073286)is 651 bp long. Bioinformatics analysis results show that, The i-dentity of the nucleotide sequence with Medicago sativa up to 99%, Can encode 216 amino acids. The analysis of the amino acid sequence of MvDREB protein shows that the protein belonging to the family of AP2 / ERF hy-drophilic nucleoprotein. The molecular weight is 24873.1, and theory pI is 5.90, instability parameter is 45.07.
Keywords:Medicago  varia  xinmu-1  MvDREB  Sequence analysis
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