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Cited by 698

The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.

The Proliferation-Quiescence Decision Is Controlled by a Bifurcation in CDK2 Activity at Mitotic Exit

Open access
Spencer, Sabrina L., Cappell, Steven D., Tsai, Feng-Chiao, Overton, K. Wesley, Wang, Clifford L., Meyer, Tobias·2013·Cell

Abstract

SUMMARY Tissue homeostasis in metazoans is regulated by transitions of cells between quiescence and proliferation. The hallmark of proliferating populations is progression through the cell cycle, which is driven by cyclin-dependent kinase (CDK) activity. Here, we introduce a live-cell sensor for CDK2 activity and unexpectedly found that proliferating cells bifurcate into two populations as they exit mitosis. Many cells immediately commit to the next cell cycle by building up CDK2 activity from an intermediate level, while other cells lack CDK2 activity and enter a transient state of quiescence. This bifurcation is directly controlled by the CDK inhibitor p21 and is regulated by mitogens during a restriction window at the end of the previous cell cycle. Thus, cells decide at the end of mitosis to either start the next cell cycle by immediately building up CDK2 activity or to enter a transient G0-like state by suppressing CDK2 activity.

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Crossref · 10.1016/j.cell.2013.08.062

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Metadata

Authors
Spencer, S. L., Cappell, S. D., Tsai, F.-C., Overton, K. W., Wang, C. L., & Meyer, T.
Venue
Cell
Publisher
Elsevier BV
Published
2013-10
Volume
155
Issue
2
Pages
369-383
ISSN
0092-8674 (ISSN-L)
OpenAlex
W2065782380
Cited by
698
References
6
FWCI
15.65
Type
journal article
Language
en
Open access
bronze

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.