大豆吡哆醇生物合成蛋白基因(PDX)的电子克隆和进化分析  

In Silico Cloning of Pyridoxine Biosynthesis Protein Gene from Soybean and Evolution Analysis

作　　者：李蕊[1] 孟宪萍[1] 胡英考[1] 蔡民华[1] 李雅轩[1] 

机构地区：[1]首都师范大学生命科学学院,北京100037

出　　处：《华北农学报》2007年第1期64-68,共5页Acta Agriculturae Boreali-Sinica

基　　金：北京市教委科技发展计划项目基金资助(200310028112)

摘　　要：电子克隆（In silicocloning）是随着基因组计划和EST计划实施而发展起来的利用生物信息学手段进行基因克隆的新方法。根据物种间同源基因相对保守的特点,以拟南芥（Arabidopsis thaliana）吡哆醇生物合成蛋白cDNA序列为信息探针,对大豆（Glycine max）EST数据库进行同源搜索和序列拼接,获得了1 280 bp长的大豆吡哆醇生物合成蛋白的基因序列（GenBank登陆号为DQ139265）。经过RT-PCR扩增、基因组PCR扩增、分子克隆和序列分析验证,结果表明与电子克隆序列完全一致。该基因具有完整的开放阅读框架（ORF,20~955 bp）,编码311个氨基酸。通过与水稻、日本百脉根、烟草、截形苜蓿等物种的吡哆醇生物合成蛋白序列比对,发现该基因具有高度的保守性。表明根据物种间同源基因序列,对跨物种间EST数据库进行同源检索、筛选、拼接,是克隆基因的有效途径。In silico cloning is developing with the project of genomic and EST. It is a new method of gene-cloning through bioinformatics. A query probe from the eDNA sequence of Arabidopsis thaliana pyridoxine biosynthesis protein was designed to blast Glycine max EST database according to the relative conservation of homologous genes and a soybean PDX gene eDNA of 1 280 bp was obtained （GenBank Accession, DQ139265）. This sequence was confirmed by RT- PCR, genomic PCR, molecular cloned and sequenced. It contained a complete ORF, from 20 to 955 bp, encoded 311amino acids, and conserved with Arabidopsis thaliana, Oryza sativa, Lotus corniculatus var. tabacum, Medicago truncatula and Triticum aestivum. The results showed that it was an efficient genes by searching EST database with homologous gene of model species japonicus , Nicotiana technique to clone new genes by searching EST database with homologous gene of model species.

关 键 词：电子克隆 EST数据库 RT-PCR 基因组PCR 大豆 吡哆醇生物合成蛋白 

分 类 号：S565.1[农业科学—作物学]