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牛Pbx-1基因的电子克隆及生物信息学分析
引用本文:刘卉玲,崔群维,吴国良,范睿,蔡亚非,王根林.牛Pbx-1基因的电子克隆及生物信息学分析[J].激光生物学报,2009,18(1).
作者姓名:刘卉玲  崔群维  吴国良  范睿  蔡亚非  王根林
作者单位:1. 安徽师范大学生物环境与生态安全安徽省高校重点实验室,安徽,芜湖,241000;安徽师范大学生物重要生物资源保护与利用研究重点实验室,安徽,芜湖,241000
2. 南京农业大学动物科技学院,江苏,南京,210095
基金项目:国家科技支撑计划,芜湖市科技计划重点项目,安徽省自然科学基金 
摘    要:新基因全长cDNA序列很难获得,但电子克隆却提供了基因克隆的一种策略.利用小鼠Pbx-1基因编码序列(NM_183355)为种子序列进行电子克隆获得牛Pbx-1基因完整编码序列.然后,用生物信息学方法分析了牛的Pbx-1基因的结构,密码子偏性和氨基酸的同源性等.结果表明:该基因cDNA全长1 754 bp,无内含子,最大开放阅读框1 305 bp.编码434个氨基酸.预测其编码的蛋白分子量为47 189.5 Da,与小鼠的同源性为81%.

关 键 词:牛Pbx-1基因  电子克隆  生物信息学

In Silico Cloning and Bioinformatics Analysis of the Cattle Pbx-1 Gene
LIU Hui-ling,CUI Qun-wei,WU Guo-liang,FAN Rui,CAI Ya-fei,WANG Gen-lin.In Silico Cloning and Bioinformatics Analysis of the Cattle Pbx-1 Gene[J].ACTA Laser Biology Sinica,2009,18(1).
Authors:LIU Hui-ling  CUI Qun-wei  WU Guo-liang  FAN Rui  CAI Ya-fei  WANG Gen-lin
Institution:1.Anhui Normal University a.Key Laboratory of Biotic Environment and Ecological Safety in Anhui Province;b.Provincial Key Laboratory of Conservation and Exploitation of Biological Resources;Wuhu 241000;Anhui;China;2.Animal Science and Technology;College of Nanjing Agricultural University;Nanjing 210095;Jiangsu;China
Abstract:It is not easy to obtain the full-length cDNA sequence of a novel gene,however,in silico cloning provides a strategy for gene cloning.The complete coding sequence of cattle Pbx-1 gene was obtained by using mouse Pbx-1 gene coding sequence(NM_183355) as seeded sequence in silico cloning.Afterwards,the structure and codon adaptation of Pbx-1,and amino acid homology of Pbx-1 protein in cattle was analyzed by using bioinformatics methods.The results show that the cDNA of cattle Pbx-1 gene is 1 754 bp with no in...
Keywords:cattle Pbx-1 gene  in silico cloning  bioinformatics  
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