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PMID: 7871434 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A p53-dependent mouse spindle checkpoint.

Science (New York, N.Y.) ·Vol. 267 ·No. 5202 ·1995-03-03 ·Pages 1353-6

Cross SM, Sanchez CA, Morgan CA, Schimke MK, Ramel S, Idzerda RL, Raskind WH, Reid BJ

Abstract

Cell cycle checkpoints enhance genetic fidelity by causing arrest at specific stages of the cell cycle when previous events have not been completed. The tumor suppressor p53 has been implicated in a G1 checkpoint. To investigate whether p53 also participates in a mitotic checkpoint, cultured fibroblasts from p53-deficient mouse embryos were exposed to spindle inhibitors. The fibroblasts underwent multiple rounds of DNA synthesis without completing chromosome segregation, thus forming tetraploid and octaploid cells. Deficiency of p53 was also associated with the development of tetraploidy in vivo. These results suggest that murine p53 is a component of a spindle checkpoint that ensures the maintenance of diploidy.

Related Genes
p53
MeSH Terms
Animals Cell Cycle Cells, Cultured DNA/biosynthesis Demecolcine/pharmacology Diploidy Female Genes, p53 Male Mice Mitosis Nocodazole/pharmacology Ploidies Spindle Apparatus/physiology Tumor Suppressor Protein p53/physiology
Chemicals
Tumor Suppressor Protein p53 DNA Nocodazole Demecolcine
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Cross S M
Department of Medicine, University of Washington, Seattle 98195.
Sanchez C A
Morgan C A
Schimke M K
Ramel S
Idzerda R L
Raskind W H
Reid B J
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1995-03-03
Pages
1353-6
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NCI NIH HHS · R01CA55814 · United States
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