Role of the Protein Chaperone YDJ1 in Establishing Hsp90-Mediated Signal Transduction Pathways
- 2 June 1995
- journal article
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 268 (5215) , 1362-1365
- https://doi.org/10.1126/science.7761857
Abstract
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 on 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.Keywords
This publication has 23 references indexed in Scilit:
- Mutations in Hsp83 and cdc37 impair signaling by the sevenless receptor tyrosine kinase in DrosophilaCell, 1994
- Assisting spontaneity: the role of Hsp90 and small Hsps as molecular chaperonesTrends in Biochemical Sciences, 1994
- Dynamics of heat shock protein 90-progesterone receptor binding and the disactivation loop model for steroid receptor complexesMolecular Endocrinology, 1993
- Torso, a receptor tyrosine kinase required for embryonic pattern formation, shares substrates with the sevenless and EGF-R pathways in Drosophila.Genes & Development, 1993
- Steroid receptors and their associated proteinsMolecular Endocrinology, 1993
- Characterization of SIS1, a Saccharomyces cerevisiae homologue of bacterial dnaJ proteins.The Journal of cell biology, 1991
- Characterization of YDJ1: a yeast homologue of the bacterial dnaJ protein.The Journal of cell biology, 1991
- Reduced levels of hsp90 compromise steroid receptor action in vivoNature, 1990
- A movable and regulable inactivation function within the steroid binding domain of the glucocorticoid receptorCell, 1988
- Mammalian Glucocorticoid Receptor Derivatives Enhance Transcription in YeastScience, 1988