A YEAST SYSTEM FOR EXPRESSION OF HUMAN CYSTATHIONINE BETA-SYNTHASE - STRUCTURAL AND FUNCTIONAL CONSERVATION OF THE HUMAN AND YEAST GENES

被引:70
作者
KRUGER, WD
COX, DR
机构
[1] Department of Psychiatry, Univ. of California at San Francisco, San Francisco
[2] Department of Genetics, School of Medicine, Stanford University, Stanford
关键词
HOMOCYSTINURIA; INHERITED METABOLIC DISORDER; SACCHAROMYCES CEREVISIAE; CYS4;
D O I
10.1073/pnas.91.14.6614
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Human cystathionine beta-synthase (CBS; EC 4.2.1.22) deficiency results in a recessive genetic disorder whose clinical and biochemical manifestations vary greatly among affected individuals. In an effort to identify and analyze mutations in the human CBS gene, we have developed a yeast expression system for human CBS. We have cloned and sequenced a human cDNA that codes for CBS and have expressed the human CBS protein in yeast cells lacking endogenous CBS. The human enzyme produced in yeast is functional both in vitro and in vivo. We have also cloned and sequenced the yeast gene, CYS4, that codes for CBS. The predicted human and yeast CBS proteins are 38% identical and 72% similar to each other, as well as sharing significant similarity with bacterial cysteine synthase. These results demonstrate the evolutionary conservation of CBS and establish the utility of a yeast expression system for studying human CBS.
引用
收藏
页码:6614 / 6618
页数:5
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