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The mammalian CHORD-containing protein melusin is a stress response protein interacting with Hsp90 and Sgt1.
- Source :
-
FEBS letters [FEBS Lett] 2008 Jun 11; Vol. 582 (13), pp. 1788-94. Date of Electronic Publication: 2008 May 12. - Publication Year :
- 2008
-
Abstract
- Melusin is a mammalian muscle specific CHORD containing protein capable of activating signal transduction pathways leading to cardiomyocytes hypertrophy in response to mechanical stress. To define melusin function we searched for molecular partners possibly involved in melusin dependent signal transduction. Here we show that melusin and heat shock proteins are co-regulated. Moreover, melusin directly binds to Hsp90, a ubiquitous chaperone involved in regulating several signaling pathways. In addition, melusin interacts with Sgt1, an Hsp90 binding molecule. Melusin does not behave as an Hsp90 substrate but rather as a chaperone capable to protect citrate synthase from heat induced aggregation. These results describe melusin as a new component of the Hsp90 chaperone machinery.
- Subjects :
- Adaptor Proteins, Signal Transducing
Animals
Cell Cycle Proteins genetics
Cytoskeletal Proteins genetics
Gene Expression Profiling
Gene Expression Regulation
HSP90 Heat-Shock Proteins genetics
Immunoprecipitation
Mice
Molecular Chaperones genetics
Muscle Proteins genetics
Protein Structure, Tertiary
Cell Cycle Proteins metabolism
Cytoskeletal Proteins metabolism
HSP90 Heat-Shock Proteins metabolism
Molecular Chaperones metabolism
Muscle Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0014-5793
- Volume :
- 582
- Issue :
- 13
- Database :
- MEDLINE
- Journal :
- FEBS letters
- Publication Type :
- Academic Journal
- Accession number :
- 18474241
- Full Text :
- https://doi.org/10.1016/j.febslet.2008.04.058