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Updated: May 16, 2026

Studying Proteolysis of Cyclin B at the Single Cell Level in Whole Cell Populations
Published on: September 17, 2012
A cyclin without cyclin-dependent kinases: cyclin F controls genome stability through ubiquitin-mediated proteolysis
Vincenzo D'Angiolella1, Mine Esencay, Michele Pagano
1Department of Pathology, NYU Cancer Institute, New York University School of Medicine, New York, NY 10016, USA. vincenzo.d'angiolella@nyumc.org
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.
Insights
Cyclin F controls genome stability by targeting key proteins for degradation. This ubiquitin-mediated proteolysis is crucial for cell cycle regulation and has implications for cancer development.
Area of Science:
- Molecular Biology
- Cell Biology
- Biochemistry
Background:
- Cell cycle progression relies on cyclin-dependent kinases (CDKs) and their cyclin partners.
- Cyclin F, a unique cyclin, functions as a substrate recognition subunit in SCF ubiquitin ligase complexes.
- The F-box protein family, including Cyclin F, plays a critical role in protein degradation pathways.
Purpose of the Study:
- To elucidate the distinct catalytic activity and substrate recruitment strategy of Cyclin F.
- To identify novel substrates targeted by the SCF(Cyclin F) complex.
- To highlight the role of Cyclin F in maintaining genome stability and its link to cancer.
Main Methods:
- Analysis of Cyclin F's unique substrate recruitment mechanism.
- Identification of SCF(Cyclin F) substrates involved in essential cellular processes.
- Investigation of ubiquitin-mediated proteolysis regulated by Cyclin F.
Main Results:
- Cyclin F targets substrates involved in deoxyribonucleotide triphosphate (dNTP) production.
- SCF(Cyclin F) regulates centrosome duplication and spindle formation.
- Cyclin F's function is critical for controlling genome stability.
Conclusions:
- Cyclin F's role as an F-box protein is central to its function in ubiquitin-mediated proteolysis.
- Dysregulation of Cyclin F substrates impacts genome stability and cancer development.
- Understanding Cyclin F pathways offers insights into potential cancer therapeutics.
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