首页 | 本学科首页   官方微博 | 高级检索  
     检索      

绵羊regakine-1基因的克隆与序列分析
引用本文:乔新安,杨国宇,王艳玲,王月影,韩立强,都军霞.绵羊regakine-1基因的克隆与序列分析[J].中国农学通报,2007,23(8):40-40.
作者姓名:乔新安  杨国宇  王艳玲  王月影  韩立强  都军霞
作者单位:河南农业大学动物生理生化实验室,郑州,450002
基金项目:河南省重点科技攻关项目"乳汁体细胞分子生物学技术平台的建立与应用"(0523010500).
摘    要:【研究目的】克隆并分析绵羊regakine-1基因;【方法】肠系膜淋巴结组织提取总RNA,利用设计的引物进行RT-PCR,PCR产物与pMD-19T载体连接后转化JM109感受态细胞,筛选阳性克隆、测序,并进行序列分析;【结果】克隆的绵羊regakine-1基因与牛的同源性为91%,推测的氨基酸序列信号肽为1~21aa,SCY结构域为29~87aa,结构特征与牛的相一致。【结论】克隆了绵羊regakine-1基因的ORF,并注册GenBank (AccessionEF617337)

关 键 词:陕北农牧交错带  陕北农牧交错带  粮食安全  植物性产品  动物性产品  
修稿时间:2007-05-262007-06-07

Molecular Cloning and Sequence Analysis of Ovine Regakine-1
Qiao Xinan,Yang Guoyu,Wang Yanling,Wang Yueying,Han Liqiang,Du Junxia.Molecular Cloning and Sequence Analysis of Ovine Regakine-1[J].Chinese Agricultural Science Bulletin,2007,23(8):40-40.
Authors:Qiao Xinan  Yang Guoyu  Wang Yanling  Wang Yueying  Han Liqiang  Du Junxia
Institution:(Lab of Animal Physiology & Biochemistry Henan Agricultural University, Zhengzhou 450002)
Abstract:OBJECTIVE]To clone and analysis the ovine regakine-1.METHOD]Total RNA was extracted from mesenteric lymph node and mRNA sequence of gene were amplified by RT-PCR with designed primers. The PCR products were ligated into the pMD-19T vector, and then transformed into competent cells of JM109. The recombinant plasmid was identified and the sequence was analyzed.RESULTS]Identity analysis showed that the regakine-1 nucleotide sequence shared 91% homology with that of cattle. The signal peptide of predicted amino acid sequence is 1~21aa and the structural domain SCY is 29~87aa, revealing that the structural feature is consistent with cattle regakine-1.CONCHUSION]The ovine ORF of regakine-1 gene was successfully cloned in present study and the sequence has been submitted to GenBank(Accession. EF617337).
Keywords:Ovine  Regakine-1  Molecular Cloning  Sequence Analysis
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《中国农学通报》浏览原始摘要信息
点击此处可从《中国农学通报》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号