Role of Sst2 in modulating G protein-coupled receptor signaling

被引:33
|
作者
Shah, A [1 ]
Marsh, L [1 ]
机构
[1] ALBERT EINSTEIN COLL MED,DEPT CELL BIOL,BRONX,NY 10461
关键词
D O I
10.1006/bbrc.1996.1340
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
Sst2 formally acts as an inhibitor of G protein-coupled receptor signaling in yeast perhaps stabilizing a G protein/unactivated receptor complex. desTrp1, Ala3 alpha-factor (dTA-alpha f), normally a competitive antagonist, activated responses in an sst2 strain. The antagonist to agonist switch was consistent with an Sst2 effect on receptor/G protein coupling, but not with an Sst2 role in global reduction of signaling, Response to alpha-factor, assayed by growth arrest, was independent of level of expressed surface receptor over a 40-fold range in an SST2(+) strain, consistent with coupling of only a subset of receptors to G protein. In contrast, in an sst2 strain, response to alpha-factor was proportional to receptor expression, consistent with participation of all receptors in signaling. The wt alpha-factor receptor inhibited signaling in response to dTA-alpha f when introduced into a CKC4 chimeric receptor strain. The dominant-negative effect of the receptor might reflect sequestration of G protein. (C) 1996 Academic Press, Inc.
引用
收藏
页码:242 / 246
页数:5
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