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Proteomic analysis of the response to cell cycle arrests in human myeloid leukemia cells
被引:34
|作者:
Ly, Tony
[1
]
Endo, Aki
[1
]
Lamond, Angus I.
[1
]
机构:
[1] Univ Dundee, Coll Life Sci, Ctr Gene Regulat & Express, Dundee, Scotland
来源:
ELIFE
|
2015年
/
4卷
基金:
英国生物技术与生命科学研究理事会;
欧洲研究理事会;
英国惠康基金;
关键词:
REPLICATION;
QUIESCENCE;
HYDROXYUREA;
EXPRESSION;
G2;
D O I:
10.7554/eLife.04534
中图分类号:
Q [生物科学];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Previously, we analyzed protein abundance changes across a 'minimally perturbed' cell cycle by using centrifugal elutriation to differentially enrich distinct cell cycle phases in human NB4 cells (Ly et al., 2014). In this study, we compare data from elutriated cells with NB4 cells arrested at comparable phases using serum starvation, hydroxyurea, or RO-3306. While elutriated and arrested cells have similar patterns of DNA content and cyclin expression, a large fraction of the proteome changes detected in arrested cells are found to reflect arrest-specific responses (i.e., starvation, DNA damage, CDK1 inhibition), rather than physiological cell cycle regulation. For example, we show most cells arrested in G2 by CDK1 inhibition express abnormally high levels of replication and origin licensing factors and are likely poised for genome re-replication. The protein data are available in the Encyclopedia of Proteome Dynamics (http://www.peptracker.com/epd/), an online, searchable resource.
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页数:15
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