ROLE OF THE PROTEIN CHAPERONE YDJ1 IN ESTABLISHING HSP90-MEDIATED SIGNAL-TRANSDUCTION PATHWAYS

被引:216
作者
KIMURA, Y
YAHARA, I
LINDQUIST, S
机构
[1] UNIV CHICAGO, DEPT MOLEC GENET & CELL BIOL, CHICAGO, IL 60637 USA
[2] UNIV CHICAGO, HOWARD HUGHES MED INST, CHICAGO, IL 60637 USA
[3] TOKYO METROPOLITAN INST MED SCI, TOKYO 113, JAPAN
关键词
D O I
10.1126/science.7761857
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
The substrate-specific protein chaperone Hsp90 (heat shock protein 90) from Saccharomyces cerevisiae functions in diverse signal transduction pathways. A mutation in YDJ1, a member of the DnaJ chaperone family, was recovered in a synthetic-lethal screen with Hsp90 mutants. in an otherwise wild-type background, the ydj1 mutation exerted strong and specific effects an three Hsp90 substrates, derepressing two (the estrogen and glucocorticoid receptors) and reducing the function of the third (the tyrosine kinase p60(v-src)). Analysis of one of these substrates, the glucocorticoid receptor, indicated that Ydj1 exerts its effects through physical interaction with Hsp90 substrates.
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页码:1362 / 1365
页数:4
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