期刊
NATURE COMMUNICATIONS
卷 6, 期 -, 页码 -出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms7533
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资金
- Danish Council for Independent Research [FSS: 12-126108, FNU: 12-127136]
- EMBO Young Investigator programme
- Novo Nordisk Foundation
- CRUK project grant
- Royal Society Dorothy Hodgkin Fellowship
- MRC Senior Research Fellowship
- EMBO Young Investigator Award
- European Research Council [ERC2011StG, 281,765]
- Danish National Research Foundation [DNRF82]
- Lundbeck Foundation
- Danish Cancer Society
- Danish Medical Research Council
- Villum Kann Rasmussen Foundation
- European Research Council (ERCStG) [242905]
- Carlsberg Foundation
- Fundacao para a Ciencia e a Tecnologia
- Novo Nordisk Foundation Center for Protein Research [PI Chunaram Choudhary] Funding Source: researchfish
- European Research Council (ERC) [242905] Funding Source: European Research Council (ERC)
DNA replication stress is a source of genomic instability. Here we identify changed mutation rate 1 (Cmr1) as a factor involved in the response to DNA replication stress in Saccharomyces cerevisiae and show that Cmr1-together with Mrc1/Claspin, Pph3, the chaperonin containing TCP1 (CCT) and 25 other proteins-define a novel intranuclear quality control compartment (INQ) that sequesters misfolded, ubiquitylated and sumoylated proteins in response to genotoxic stress. The diversity of proteins that localize to INQ indicates that other biological processes such as cell cycle progression, chromatin and mitotic spindle organization may also be regulated through INQ. Similar to Cmr1, its human orthologue WDR76 responds to proteasome inhibition and DNA damage by relocalizing to nuclear foci and physically associating with CCT, suggesting an evolutionarily conserved biological function. We propose that Cmr1/WDR76 plays a role in the recovery from genotoxic stress through regulation of the turnover of sumoylated and phosphorylated proteins.
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