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PMID: 9572732 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

The biochemical basis of an all-or-none cell fate switch in Xenopus oocytes.

Science (New York, N.Y.) ·Vol. 280 ·No. 5365 ·1998-05-08 ·Pages 895-8

Ferrell JE, Machleder EM

Abstract

Xenopus oocytes convert a continuously variable stimulus, the concentration of the maturation-inducing hormone progesterone, into an all-or-none biological response-oocyte maturation. Here evidence is presented that the all-or-none character of the response is generated by the mitogen-activated protein kinase (MAPK) cascade. Analysis of individual oocytes showed that the response of MAPK to progesterone or Mos was equivalent to that of a cooperative enzyme with a Hill coefficient of at least 35, more than 10 times the Hill coefficient for the binding of oxygen to hemoglobin. The response can be accounted for by the intrinsic ultrasensitivity of the oocyte's MAPK cascade and a positive feedback loop in which the cascade is embedded. These findings provide a biochemical rationale for the all-or-none character of this cell fate switch.

MeSH Terms
Animals Carrier Proteins/pharmacology Cell Cycle Cycloheximide/pharmacology Enzyme Activation Feedback Kinetics Maltose-Binding Proteins Mitogen-Activated Protein Kinase 1/metabolism Oocytes/cytology,drug effects,enzymology,metabolism Phosphorylation Progesterone/pharmacology Protein Synthesis Inhibitors/pharmacology Proto-Oncogene Proteins c-mos/pharmacology Recombinant Fusion Proteins/pharmacology
Chemicals
Carrier Proteins Maltose-Binding Proteins Protein Synthesis Inhibitors Recombinant Fusion Proteins Progesterone Cycloheximide Proto-Oncogene Proteins c-mos Mitogen-Activated Protein Kinase 1
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Ferrell J E
Department of Molecular Pharmacology, Stanford University School of Medicine, Stanford, CA 94305-5332, USA. [email protected]
Machleder E M
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1998-05-08
Pages
895-8
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NCI NIH HHS · CA09302 · United States
NIGMS NIH HHS · GM56383 · United States
Corrections
CommentIn
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