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Mammalian cell-cycle regulation: Several cdks, numerous cyclins and diverse compensatory mechanisms

*Corresponding author for this work
  • National Institutes of Health
    ,
  • Agency for Science, Technology and Research, Singapore
Scholary Output:
Contribution to journal
Review article
Peer-review

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

After a decade of extensive work on gene knockout mouse models of cell-cycle regulators, the classical model of cell-cycle regulation was seriously challenged. Several unexpected compensatory mechanisms were uncovered among cyclins and Cdks in these studies. The most astonishing observation is that Cdk2 is dispensable for the regulation of the mitotic cell cycle with both Cdk4 and Cdk1 covering for Cdk2's functions. Similar to yeast, it was recently discovered that Cdk1 alone can drive the mammalian cell cycle, indicating that the regulation of the mammalian cell cycle is highly conserved. Nevertheless, cell-cycle-independent functions of Cdks and cyclins such as in DNA damage repair are still under investigation. Here we review the compensatory mechanisms among major cyclins and Cdks in mammalian cell-cycle regulation.

Publication Information

Output type

Scholary Output:
Contribution to journal
Review article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 2925-2939 (15 pages)

Journal (Volume, Issue Number)

Oncogene (Volume 28, Issue 33)

Publication milestones

  • Published - 08/20/2009

Publication status

Published - 08/20/2009

ISSN

0950-9232

Publication IDs

  • Scopus: 69249230769
  • PubMed: 19561645

Publication metrics

Metrics

SciVal
FWCI
5.44
SciVal
Author count
2
SciVal
citations
474
SciVal
Paper percentile
99
SciVal
Top percentile
1
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
1
Scopus
citations

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Captures
798
Mentions
7
Citation count
680

Funding Details

We thank Kaldis lab members for discussions and support. This research was supported by A*STAR of Singapore (PK) and the Intramural Research Program of the NIH, National Cancer Institute, Center for Cancer Research (AS).
FundersFunding numbers
NIH
-
NCI
-
A*STAR
-