人类生精相关基因TSARG4的cDNA克隆

被引:5
作者
邢晓为
李麓芸
傅俊江
朱文兵
刘刚
刘上峰
卢光琇
机构
[1] 中南大学湘雅医学院人类生殖工程研究室
关键词
基因克隆; 间隙填充法; 逆转录聚合酶反应; 睾丸; 组织表达谱;
D O I
暂无
中图分类号
Q987 [人类遗传学];
学科分类号
071007 ;
摘要
为了探索精子生成的分子机制 ,从人精子外部致密纤维蛋白相关基因SPAG4(spermantigen 4)和小鼠精母细胞中表达的AK0 0 62 2 5基因出发 ,找到两个人类EST ,BG72 0 5 64和AI70 0 45 4,其中BG72 0 5 64在人睾丸中表达。运用“间隙填充法”填平这两个EST之间的间隙 ,从人睾丸文库中快速克隆了同源于SPAG4和AK0 0 62 2 5基因的人类TSARG4基因 (testisandspermatogenesisrelatedgene 4) (GenBank登录号为AF40 13 5 0 ) ,并用RT PCR对该基因阅读框进行验证。TSARG4基因全长 12 5 2bp ,开放阅读框为 94~ 12 3 3bp ,定位于 2 0q11.2 ,推定编码 3 79个氨基酸 ,预计分子量为 43 0 81.45 ,等电点为 8.61,该基因与小鼠精母细胞基因AK0 0 62 2 5编码的氨基酸序列同源性 74% ,与人类SPAG4基因编码的氨基酸序列同源性 45 %。RT PCR表明人类TSARG4基因在多个组织中均有表达 ,而同源的小鼠AK0 0 62 2 5基因仅在睾丸中表达
引用
收藏
页码:283 / 288
页数:6
相关论文
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