MOLECULAR-CLONING AND SEQUENCING OF GENOMIC DNA ENCODING YEAST VACUOLAR CARBOXYPEPTIDASE YSCS

被引:13
|
作者
BORDALLO, J [1 ]
BORDALLO, C [1 ]
GASCON, S [1 ]
SUAREZRENDUELES, P [1 ]
机构
[1] UNIV OVIEDO, DEPT BIOL FUNC, AREA BIOQUIM & BIOL MOLEC, E-33071 OVIEDO, SPAIN
来源
FEBS LETTERS | 1991年 / 283卷 / 01期
关键词
CARBOXYPEPTIDASE; MOLECULAR CLONING; VACUOLE; YEAST;
D O I
10.1016/0014-5793(91)80546-F
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A Saccharomyces cerevisiae genomic DNA encoding vacuolar carboxypeptidase yscS was cloned from a yeast YEp13 library by complementation of the previously characterized mutation cps1-1 [(1981) J. Bacteriol. 147, 418-426], by means of staining carboxypeptidase activity in yeast colonies. The nucleotide sequence of the cloned gene was determined. The open reading frame of CPS1 consists of 576 codons and therefore encodes a protein of 64961 molecular weight. A stretch of 19 residues near the N-terminus of the deduced polypeptide sequence contains characteristics common to known hydrophobic leader sequences. CPS1 was determined by DNA blot analysis to be a single copy gene located on chromosome X. The cloned fragment was used to identify a 2.1 kb mRNA. A transcriptional activation of CPS1 occurs when cells grow on a substrate of carboxypeptidase yscS as sole nitrogen source.
引用
收藏
页码:27 / 32
页数:6
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