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通过在酿酒酵母中对ade2 - 101突变体进行互补作用克隆和测序编码嘌呤途径多功能多肽的人类cDNA。

Cloning and sequencing of a human cDNA coding for a multifunctional polypeptide of the purine pathway by complementation of the ade2-101 mutant in Saccharomyces cerevisiae.

作者信息

Minet M, Lacroute F

机构信息

Centre de Génétique Moléculaire, C.N.R.S., Gif sur Yvette, France.

出版信息

Curr Genet. 1990 Nov;18(4):287-91. doi: 10.1007/BF00318209.

DOI:10.1007/BF00318209
PMID:2253271
Abstract

A HeLa cell cDNA library on a yeast expression vector was used to complement auxotrophic markers of Saccharomyces cerevisiae. Clones complementing the ade2-101 mutation harbor a 1.5 kb poly(A)+ tailed insert with a 425 amino acid open reading frame hybridizing with two human mRNAs of 1.5 kb and 3.1 kb. Its 5' half is homologous to Bacillus subtilis SAICAR synthetase (E.C.6.3.2.6.) and its 3' terminal half corresponds to the catalytic subunit of Escherichia coli and B. subtilis AIR carboxylase (E.C.4.1.1.21). In agreement with these homologies, pADE2H1 clones complement both ade1 and ade2 mutants of S. cerevisiae, as was also recently reported for a 3.1 kb cDNA isolated from human hepatocytes.

摘要

利用酵母表达载体上的HeLa细胞cDNA文库来互补酿酒酵母的营养缺陷型标记。互补ade2-101突变的克隆含有一个1.5 kb的聚腺苷酸加尾插入片段,其开放阅读框为425个氨基酸,可与两条分别为1.5 kb和3.1 kb的人mRNA杂交。其5'端一半与枯草芽孢杆菌SAICAR合成酶(E.C.6.3.2.6.)同源,3'端一半与大肠杆菌和枯草芽孢杆菌AIR羧化酶的催化亚基(E.C.4.1.1.21)对应。与这些同源性一致,pADE2H1克隆可互补酿酒酵母的ade1和ade2突变体,最近从人肝细胞中分离出的一个3.1 kb cDNA也有此报道。

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Cloning and sequencing of a human cDNA coding for a multifunctional polypeptide of the purine pathway by complementation of the ade2-101 mutant in Saccharomyces cerevisiae.通过在酿酒酵母中对ade2 - 101突变体进行互补作用克隆和测序编码嘌呤途径多功能多肽的人类cDNA。
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