Disassembly of transcriptional regulatory complexes by molecular chaperones.

Article Details

Citation

Freeman BC, Yamamoto KR

Disassembly of transcriptional regulatory complexes by molecular chaperones.

Science. 2002 Jun 21;296(5576):2232-5.

PubMed ID
12077419 [ View in PubMed
]
Abstract

Many biological processes are initiated by cooperative assembly of large multicomponent complexes; however, mechanisms for modulating or terminating the actions of these complexes are not well understood. For example, hormone-bound intracellular receptors (IRs) nucleate formation of transcriptional regulatory complexes whose actions cease promptly upon hormone withdrawal. Here, we show that the p23 molecular chaperone localizes in vivo to genomic response elements in a hormone-dependent manner, disrupting receptor-mediated transcriptional activation in vivo and in vitro; Hsp90 weakly displayed similar activities. Indeed, p23 and Hsp90 also disrupted the activities of some non-IR-containing transcriptional regulatory complexes. We suggest that molecular chaperones promote disassembly of transcriptional regulatory complexes, thus enabling regulatory machineries to detect and respond to signaling changes.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Prostaglandin E synthase 3Q15185Details