期刊论文详细信息
FEBS Letters
Structural determination of Saccharomyces cerevisiae rig gene and identification of its product as ribosomal protein S21
Yonekura, Hideto1  Unno, Michiaki1  Okamoto, Hiroshi1  Tohgo, Akira1  Takasawa, Shin1 
[1] Deparment of Biochemistry, Tohoku University School of Medicine, Sendai 980, Miyagi, Japan
关键词: rig;    Ribosomal protein S21;    Chromosomal localization;    Yeast;    UASrpg;    upstream activation sequence of ribosomal protein gene(s);   
DOI  :  10.1016/0014-5793(92)80704-K
学科分类:生物化学/生物物理
来源: John Wiley & Sons Ltd.
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【 摘 要 】

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 cerevisae) 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 encodes 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.

【 授权许可】

Unknown   

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