摘要
利用微量全血直接进行PCR扩增,克隆到了猴与人的GDNF基因,经全序列分析证实人GDNF (hGDNF)基因全部正确,猴 GDNF(RhGDNF GenBank AF106678)基因与人 GDNF基因高度同源,在 DNA的 成熟蛋白编码区中二者有7个核苷酸不同,而蛋白中仅有两个氨基酸差异.该研究为GDNF的重组表达及进 一步研究GDNF蛋白的结构与生物学功能打下基础.简要探讨了全血量对PCR扩增结果的影响,并对脊椎动 物进化中GDNF的保守性作了比较.
By direct PCR from whole blood, the RhGDNF gene and hGDNF gene were cloned and sequenced. We investigated the best blood volume for PCR amplification. The sequence data of chinese hGDNF gene showed no polymorphism among different races. The sequence data of RhGCNF gene showed seven bases' difference from hGDNF gene, but only two amino acids were different.
出处
《云南大学学报(自然科学版)》
CAS
CSCD
1998年第S4期499-501,504,共4页
Journal of Yunnan University(Natural Sciences Edition)