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PMID: 2474853 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

The product of the mos proto-oncogene as a candidate "initiator" for oocyte maturation.

Science (New York, N.Y.) ·Vol. 245 ·No. 4918 ·1989-08-11 ·Pages 643-6

Sagata N, Daar I, Oskarsson M, Showalter SD, Vande Woude GF

Abstract

The endogenous c-mos product, pp39mos, is required for progesterone-induced meiotic maturation in Xenopus oocytes. Treatment of oocytes with progesterone induced a rapid increase in pp39mos that preceded both the activation of maturation promoting factor (MPF) and germinal vesicle breakdown (GVBD). Microinjection of synthetic mos RNA into oocytes activated MPF and induced GVBD in the absence of progesterone. Thus, the mos proto-oncogene product may qualify as a candidate "initiator" protein of MPF and is at least one of the "triggers" for G2 to M transition.

MeSH Terms
Animals Base Sequence Cycloheximide/pharmacology Female Growth Substances/physiology Kinetics Maturation-Promoting Factor Meiosis/drug effects Microinjections Oocytes/physiology Progesterone/pharmacology Protein Biosynthesis Proto-Oncogene Proteins/genetics,physiology Proto-Oncogene Proteins c-mos RNA/genetics Transcription, Genetic Transfection Xenopus
Chemicals
Growth Substances Proto-Oncogene Proteins Progesterone RNA Cycloheximide Proto-Oncogene Proteins c-mos Maturation-Promoting Factor
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Sagata N
BRI-Basic Research Program, National Cancer Institute, Frederick Cancer Research Facility, MD 21701.
Daar I
Oskarsson M
Showalter S D
Vande Woude G F
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1989-08-11
Pages
643-6
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NCI NIH HHS · N01-CO-74101 · United States
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