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PMID: 1809377 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Involvement of wild-type p53 protein in the cell cycle requires nuclear localization.

Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research ·Vol. 2 ·No. 12 ·1991-12-00 ·Pages 661-7

Shaulsky G, Goldfinger N, Peled A, Rotter V

Abstract

Transfection of wild-type p53 into a pre-B, p53 nonproducer cell line yielded the generation of stable clones. Although constitutively expressing the growth-suppressor wild-type p53 protein, these cells proliferate continuously in vitro. However, expression of wild-type p53 in these cells altered their cell cycle pattern and reduced their growth in vivo. When the same parental cells were transfected with a plasmid coding for a wild-type p53 lacking nuclear localization signals, a wild-type cytoplasmic p53 protein was expressed. Expression of this cytoplasmic p53 product did not exert any changes in the growth of the parental cells, suggesting that wild-type p53 affects the cell cycle only when localized in the nuclear cell compartment.

MeSH Terms
Animals Cell Cycle/physiology Cell Division/physiology Cell Fractionation Cell Line Cell Nucleus/chemistry Male Mice Mice, Inbred C57BL Neoplasm Transplantation/physiology Neoplasms, Experimental/physiopathology Precipitin Tests Transfection/genetics Tumor Suppressor Protein p53/analysis,physiology
Chemicals
Tumor Suppressor Protein p53
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Shaulsky G
Department of Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Goldfinger N
Peled A
Rotter V
Article Info
Journal
Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research
Abbr.
Cell Growth Differ
ISSN
1044-9523
Published
1991-12-00
Pages
661-7
Language
English
Region
United States
NLM ID
9100024
Subset
IM
External Links
PubMed source
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