A cyclin without cyclin-dependent kinases: cyclin F controls genome stability through ubiquitin-mediated proteolysis.

Abstract:

:Cell cycle transitions are driven by the periodic oscillations of cyclins, which bind and activate cyclin-dependent kinases (CDKs) to phosphorylate target substrates. Cyclin F uses a substrate recruitment strategy similar to that of the other cyclins, but its associated catalytic activity is substantially different. Indeed, cyclin F is the founding member of the F-box family of proteins, which are the substrate recognition subunits of Skp1-Cul1-F-box protein (SCF) ubiquitin ligase complexes. Here, we discuss cyclin F function and recently identified substrates of SCF(cyclin)(F) involved in deoxyribonucleotide triphosphate (dNTP) production, centrosome duplication, and spindle formation. We highlight the relevance of cyclin F in controlling genome stability through ubiquitin-mediated proteolysis and the implications for cancer development.

journal_name

Trends Cell Biol

journal_title

Trends in cell biology

authors

D'Angiolella V,Esencay M,Pagano M

doi

10.1016/j.tcb.2012.10.011

subject

Has Abstract

pub_date

2013-03-01 00:00:00

pages

135-40

issue

3

eissn

0962-8924

issn

1879-3088

pii

S0962-8924(12)00203-6

journal_volume

23

pub_type

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