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通过筛选酵母中的互补作用分离人糖原分支酶cDNA

Isolation of human glycogen branching enzyme cDNAs by screening complementation in yeast.

作者信息

Thon V J, Khalil M, Cannon J F

机构信息

Department of Molecular Microbiology and Immunology, School of Medicine, University of Missouri, Columbia 65212.

出版信息

J Biol Chem. 1993 Apr 5;268(10):7509-13.

PMID:8463281
Abstract

Functional complementation of the Saccharomyces cerevisiae glycogen branching enzyme deficiency was screened to isolate human cDNAs that encode this enzyme. Human hepatoma cell line HepG2-derived cDNA libraries using the pAB23BXN yeast expression vector yielded four cDNAs capable of complementing the glc3::TRP1 glycogen branching enzyme mutation. Complementation was recognized by an altered iodine-staining trait. This illustrates that interspecies complementation can be used to isolate rare plasmids from libraries by screening if there is sufficient resolution. The human and yeast glycogen branching enzymes have a 67% identical amino acid sequence over a major portion of their length. The human gene is on chromosome 3.

摘要

通过对酿酒酵母糖原分支酶缺陷进行功能互补筛选,以分离编码该酶的人类cDNA。使用pAB23BXN酵母表达载体构建人肝癌细胞系HepG2来源的cDNA文库,得到了四个能够互补glc3::TRP1糖原分支酶突变的cDNA。通过碘染色特性的改变来识别互补作用。这表明,如果有足够的分辨率,种间互补可用于通过筛选从文库中分离稀有质粒。人类和酵母糖原分支酶在其大部分长度上具有67%相同的氨基酸序列。人类基因位于3号染色体上。

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