The JAMM motif of human deubiquitinase Poh1 is essential for cell viability

Poh1 deubiquitinase activity is required for proteolytic processing of polyubiquitinated substrates by the 26S proteasome, linking deubiquitination to complete substrate degradation. Poh1 RNA interference (RNAi) in HeLa cells resulted in a reduction in cell viability and an increase in polyubiquitin...

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Vydáno v:Molecular cancer therapeutics Ročník 6; číslo 1; s. 262
Hlavní autoři: Gallery, Melissa, Blank, Jonathan L, Lin, Yinghui, Gutierrez, Juan A, Pulido, Jacqueline C, Rappoli, David, Badola, Sunita, Rolfe, Mark, Macbeth, Kyle J
Médium: Journal Article
Jazyk:angličtina
Vydáno: United States 01.01.2007
Témata:
Amino Acid Motifs
Cell Survival
HeLa Cells
Humans
Mutant Proteins - metabolism
Proteasome Endopeptidase Complex - chemistry
Proteasome Endopeptidase Complex - deficiency
Proteasome Endopeptidase Complex - metabolism
RNA Interference
Trans-Activators - chemistry
Trans-Activators - deficiency
Trans-Activators - metabolism
Ubiquitin - metabolism
ISSN:1535-7163
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Shrnutí:Poh1 deubiquitinase activity is required for proteolytic processing of polyubiquitinated substrates by the 26S proteasome, linking deubiquitination to complete substrate degradation. Poh1 RNA interference (RNAi) in HeLa cells resulted in a reduction in cell viability and an increase in polyubiquitinated protein levels, supporting the link between Poh1 and the ubiquitin proteasome pathway. To more specifically test for any requirement of the zinc metalloproteinase motif of Poh1 to support cell viability and proteasome function, we developed a RNAi complementation strategy. Effects on cell viability and proteasome activity were assessed in cells with RNAi of endogenous Poh1 and induced expression of wild-type Poh1 or a mutant form of Poh1, in which two conserved histidines of the proposed catalytic site were replaced with alanines. We show that an intact zinc metalloproteinase motif is essential for cell viability and 26S proteasome function. As a required enzymatic component of the proteasome, Poh1 is an intriguing therapeutic drug target for cancer.
Bibliografie:ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:1535-7163
DOI:10.1158/1535-7163.mct-06-0542