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PMID: 8035821 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Cellular ras activity is required for passage through multiple points of the G0/G1 phase in BALB/c 3T3 cells.

Molecular and cellular biology ·Vol. 14 ·No. 8 ·1994-08-00 ·Pages 5441-9

Dobrowolski S, Harter M, Stacey DW

Abstract

Microinjection experiments demonstrated a requirement for cellular ras activity late in G1. In this study, we used two separate methods to identify an additional requirement for cellular ras activity early in the G0/G1 phase of the cell cycle. Quiescent BALB/c cells were injected with anti-ras antibody prior to stimulation with serum. The cells would therefore be inhibited in progression through the cell cycle at the earliest point requiring ras function. Alternatively, cells were inhibited in late G1 as in previous studies by injecting anti-ras several hours after serum addition to quiescent cells. The injected cultures were then treated with chemical cell cycle inhibitors known to function in mid-G1. Cells injected with anti-ras prior to serum stimulation were retained at a point of ras requirement prior to the execution point of the chemical inhibitor, while cells injected 3 to 5 h after serum stimulation were retained at a point of ras requirement downstream of the execution point of the chemical inhibitor. To confirm these results, quiescent BALB/c cells were injected with anti-ras antibody prior to or several hours following serum addition. In this case, however, second injections of oncogenic ras or adenoviral E1A protein were performed to overcome the inhibitory effects of the anti-ras antibody. Cells injected prior to serum addition were clearly inhibited at an early point of Ras requirement since they required 5 or 6 h longer to enter S phase than cells injected with anti-ras antibody after serum addition.

MeSH Terms
3T3 Cells Amiloride/pharmacology Animals Bumetanide/pharmacology Butyrates/pharmacology Cell Cycle In Vitro Techniques Mice Mice, Inbred BALB C Proto-Oncogene Proteins p21(ras)/metabolism
Chemicals
Butyrates Bumetanide Amiloride Proto-Oncogene Proteins p21(ras)
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Dobrowolski S
Department of Molecular Biology, Cleveland Clinic Foundation, Ohio 44195.
Harter M
Stacey D W
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42 references, click to expand
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Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1994-08-00
Pages
5441-9
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC359063
Subset
IM
Grants
NCI NIH HHS · CA48662 · United States
NCI NIH HHS · CA53496 · United States
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