共 100 条
Emerging functions of the VCP/p97 AAA-ATPase in the ubiquitin system
被引:655
作者:

Meyer, Hemmo
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机构:
Univ Duisburg Essen, Fac Biol, Ctr Med Biotechnol, D-45117 Essen, Germany Univ Duisburg Essen, Fac Biol, Ctr Med Biotechnol, D-45117 Essen, Germany

Bug, Monika
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机构:
Univ Duisburg Essen, Fac Biol, Ctr Med Biotechnol, D-45117 Essen, Germany Univ Duisburg Essen, Fac Biol, Ctr Med Biotechnol, D-45117 Essen, Germany

Bremer, Sebastian
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h-index: 0
机构:
Univ Duisburg Essen, Fac Biol, Ctr Med Biotechnol, D-45117 Essen, Germany Univ Duisburg Essen, Fac Biol, Ctr Med Biotechnol, D-45117 Essen, Germany
机构:
[1] Univ Duisburg Essen, Fac Biol, Ctr Med Biotechnol, D-45117 Essen, Germany
关键词:
VALOSIN-CONTAINING PROTEIN;
RETICULUM-ASSOCIATED DEGRADATION;
MITOTIC GOLGI FRAGMENTS;
FRONTOTEMPORAL DEMENTIA;
DEUBIQUITINATING ENZYME;
DNA-REPLICATION;
MEMBRANE-FUSION;
PAGET-DISEASE;
VCP DISEASE;
AURORA-B;
D O I:
10.1038/ncb2407
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The ATP-driven chaperone valosin-containing protein (VCP)/p97 governs critical steps in ubiquitin-dependent protein quality control and intracellular signalling pathways. It cooperates with diverse partner proteins to help process ubiquitin-labelled proteins for recycling or degradation by the proteasome in many cellular contexts. Recent studies have uncovered unexpected cellular functions for p97 in autophagy, endosomal sorting and regulating protein degradation at the outer mitochondrial membrane, and elucidated a role for p97 in key chromatin-associated processes. These findings extend the functional relevance of p97 to lysosomal degradation and reveal a surprising dual role in protecting cells from protein stress and ensuring genome stability during proliferation.
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页码:117 / 123
页数:7
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