Inactivation of E2F3 results in centrosome amplification.

Abstract:

:The E2F family of transcription factors is critical for the control of cell cycle progression. We now show that the specific inactivation of E2F3 in mouse embryo fibroblasts (MEFs) results in a disruption of the centrosome duplication cycle. Loss of E2F3, but not E2F1, E2F2, E2F4, or E2F5 results in unregulated cyclin E-dependent kinase activity, defects in nucleophosmin B association with centrosomes, and premature centriole separation and duplication. Consequently, this defect leads to centrosome amplification, mitotic spindle defects, and aneuploidy. Our findings implicate the E2F3 transcription factor as an important link that orchestrates DNA and centrosome duplication cycles, ensuring the faithful transmission of genetic material to daughter cells.

journal_name

Cancer Cell

journal_title

Cancer cell

authors

Saavedra HI,Maiti B,Timmers C,Altura R,Tokuyama Y,Fukasawa K,Leone G

doi

10.1016/s1535-6108(03)00083-7

keywords:

subject

Has Abstract

pub_date

2003-04-01 00:00:00

pages

333-46

issue

4

eissn

1535-6108

issn

1878-3686

pii

S1535610803000837

journal_volume

3

pub_type

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