Modulation of Ras and a-factor function by carboxyl-terminal proteolysis

被引:300
作者
Boyartchuk, VL
Ashby, MN
Rine, J
机构
[1] UNIV CALIF BERKELEY, DEPT MOL & CELL BIOL, BERKELEY, CA 94720 USA
[2] ACACIA BIOSCI INC, RICHMOND, CA 94806 USA
关键词
D O I
10.1126/science.275.5307.1796
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
Prenylated proteins contain a covalently linked cholesterol intermediate near their carboxyl-termini. Maturation of most prenylated proteins involves proteolytic removal of the last three amino acids. Two genes in Saccharomyces cerevisiae, RCE1 and AFC1, were identified that appear to be responsible for this processing, The Afc1 protein is a zinc protease that participates in the processing of yeast a-factor mating pheromone. The Reel protein contributes to the processing of both Ras protein and a-factor. Deletion of both AFC1 and RCE1 resulted in the loss of proteolytic processing of prenylated proteins. Disruption of RCE1 led to defects in Ras localization and signaling and suppressed the activated phenotype associated with the allele RAS2(val19).
引用
收藏
页码:1796 / 1800
页数:5
相关论文
共 51 条
  • [51] WHISTLER JL, 1996, THESIS U CALIFORNIA