DEPENDENCE OF YPT1 AND SEC4 MEMBRANE ATTACHMENT ON BET2

被引:102
作者
ROSSI, G [1 ]
JIANG, Y [1 ]
NEWMAN, AP [1 ]
FERRONOVICK, S [1 ]
机构
[1] YALE UNIV,SCH MED,DEPT CELL BIOL,333 CEDAR ST,NEW HAVEN,CT 06510
关键词
D O I
10.1038/351158a0
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
MANY small GTP-binding proteins are synthesized as soluble proteins that are post-translationally modified as a prerequisite for membrane attachment 1. Ypt1 and Sec4 are homologous Raslike GTP-binding proteins that have been proposed to regulate the specificity of vesicular traffic at different stages of the secretory pathway by cycling on and off membranes 2-6. Here we show that BET2, initially identified as a gene required for transport from endoplasmic reticulum to Golgi apparatus in yeast 7, encodes a factor that is needed for the membrane attachment of Ypt1 and Sec4. DNA sequence analysis has revealed that Bet2 is homologous to Dpr1 (Ram1), an essential component of a protein prenyltransferase that modifies Ras 8, enabling it to attach to membranes 9,10. We propose that Bet2 modifies Ypt1 and Sec4 in an analogous manner.
引用
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页码:158 / 161
页数:4
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