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酿酒酵母rig基因的结构测定及其产物鉴定为核糖体蛋白S21

Structural determination of Saccharomyces cerevisiae rig gene and identification of its product as ribosomal protein S21.

作者信息

Takasawa S, Tohgo A, Unno M, Yonekura H, Okamoto H

机构信息

Department of Biochemistry, Tohoku University School of Medicine, Miyagi, Japan.

出版信息

FEBS Lett. 1992 Aug 3;307(3):318-23. doi: 10.1016/0014-5793(92)80704-k.

Abstract

rig was originally isolated from a rat insulinoma-derived cDNA library. The 145 amino acid sequence of the rig protein is invariant in mammalian cDNAs. In this paper, we have isolated the cDNA and genomic clones for yeast (Saccharomyces cerevisiae) rig, determined their nucleotide sequences, and identified the gene product. The gene and the mRNA encode a basic protein of 142 amino acids which has 61.3% amino acid identity with mammalian rig protein. On two-dimensional gel electrophoresis, the in vitro transcription/translation product of yeast rig cDNA co-migrated with yeast ribosomal protein S21. These results led to the conclusion that yeast rig ribosomal protein S21 and to the determination of the previously unknown primary structure of yeast S21 protein. Unlike most ribosomal protein genes of S. cerevisiae, the gene exists as a single copy in a haploid set of the yeast genome and has no intron, locating at chromosome VII or XV.

摘要

rig最初是从大鼠胰岛素瘤衍生的cDNA文库中分离出来的。rig蛋白的145个氨基酸序列在哺乳动物cDNA中是不变的。在本文中,我们分离了酵母(酿酒酵母)rig的cDNA和基因组克隆,确定了它们的核苷酸序列,并鉴定了基因产物。该基因和mRNA编码一种142个氨基酸的碱性蛋白,与哺乳动物rig蛋白具有61.3%的氨基酸同一性。在二维凝胶电泳上,酵母rig cDNA的体外转录/翻译产物与酵母核糖体蛋白S21共迁移。这些结果得出结论,酵母rig为核糖体蛋白S21,并确定了酵母S21蛋白以前未知的一级结构。与酿酒酵母的大多数核糖体蛋白基因不同,该基因在酵母基因组的单倍体组中以单拷贝形式存在,没有内含子,位于染色体VII或XV上。

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