alexa The molecular chaperone Hsp90 plays a role in the assembly and maintenance of the 26S proteasome.
Microbiology

Microbiology

Journal of Antivirals & Antiretrovirals

Author(s): Imai J, Maruya M, Yashiroda H, Yahara I, Tanaka K

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Abstract Hsp90 has a diverse array of cellular roles including protein folding, stress response and signal transduction. Herein we report a novel function for Hsp90 in the ATP-dependent assembly of the 26S proteasome. Functional loss of Hsp90 using a temperature-sensitive mutant in yeast caused dissociation of the 26S proteasome. Conversely, these dissociated constituents reassembled in Hsp90-dependent fashion both in vivo and in vitro; the process required ATP-hydrolysis and was suppressed by the Hsp90 inhibitor geldanamycin. We also found genetic interactions between Hsp90 and several proteasomal Rpn (Regulatory particle non-ATPase subunit) genes, emphasizing the importance of Hsp90 to the integrity of the 26S proteasome. Our results indicate that Hsp90 interacts with the 26S proteasome and plays a principal role in the assembly and maintenance of the 26S proteasome.
This article was published in EMBO J and referenced in Journal of Antivirals & Antiretrovirals

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