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Pin1 stabilizes Emi1 during G2 phase by preventing its association with SCF(betatrcp).
- Source :
-
EMBO reports [EMBO Rep] 2007 Jan; Vol. 8 (1), pp. 91-8. Date of Electronic Publication: 2006 Dec 08. - Publication Year :
- 2007
-
Abstract
- The anaphase-promoting complex (APC) early mitotic inhibitor 1 (Emi1) is required to induce S- and M-phase entries by stimulating the accumulation of cyclin A and cyclin B through APC(Cdh1/cdc20) inhibition. In this report, we show that Emi1 proteolysis can be induced by cyclin A/cdk (cdk for cyclin-dependent kinase). Paradoxically, Emi1 is stable during G2 phase, when cyclin A/cdk, Plx1 and SCF(betatrcp) (SCF for Skp1-Cul1-Fbox protein)--which play a role in its degradation--are active. Here, we identify Pin1 as a new regulator of Emi1 that induces Emi1 stabilization by preventing its association with SCF(betatrcp). We show that Pin1 binds to Emi1 and prevents its association with betatrcp in an isomerization-dependent pathway. We also show that Emi1-Pin1 binding is present in vivo in XL2 cells during G2 phase and that this association protects Emi1 from being degraded during this phase of the cell cycle. We propose that S- and M-phase entries are mediated by the accumulation of cyclin A and cyclin B through a Pin1-dependent stabilization of Emi1 during G2.
- Subjects :
- Animals
Cell Cycle Proteins analysis
Cell Cycle Proteins genetics
Cell Extracts chemistry
Cyclin A metabolism
Cyclin A pharmacology
Cyclin B metabolism
Cyclin B pharmacology
Cyclin-Dependent Kinases pharmacology
G2 Phase
Humans
Immunoprecipitation
Mitosis
NIMA-Interacting Peptidylprolyl Isomerase
Xenopus
Xenopus Proteins analysis
Xenopus Proteins genetics
Cell Cycle Proteins metabolism
Peptidylprolyl Isomerase metabolism
Xenopus Proteins metabolism
beta-Transducin Repeat-Containing Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1469-221X
- Volume :
- 8
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- EMBO reports
- Publication Type :
- Academic Journal
- Accession number :
- 17159919
- Full Text :
- https://doi.org/10.1038/sj.embor.7400853