4.6 Article

Speedy/RINGO regulation of CDKs in cell cycle, checkpoint activation and apoptosis

Journal

CELL CYCLE
Volume 6, Issue 10, Pages 1188-1193

Publisher

LANDES BIOSCIENCE
DOI: 10.4161/cc.6.10.4252

Keywords

cyclin-dependent kinase; speedy; RINGO; CDK2; Cdc2; cell cycle; checkpoints; apoptosis; cancer

Categories

Funding

  1. NCI NIH HHS [R01 CA090900, T32 CA009523] Funding Source: Medline

Ask authors/readers for more resources

Speedy/RINGO family members bind and activate cyclin dependent kinases (CDKs), although these proteins have no homology to known cyclin proteins. Members of this family are required for and enhance meiotic maturation, in addition to having novel roles in regulating the mitotic mammalian cell cycle and the DNA damage response. Here we discuss how the specialized functions of these proteins differ from classical cyclin-mediated activation of CDKs. Through atypical activation of CDKs, bypass of conventional inhibitory mechanisms, and unique substrate selection, Speedy/RINGO proteins contribute to cell cycle, checkpoint, and apoptotic regulation. Furthermore, we address the recently established correlation between Spy1 and cancer in terms of the specialized functions of the Speedy/RINGO family.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available