Positive Regulation of cdc2 Gene Activity by Protein Phosphatase Type 2A
Several lines of evidence indicate that serine/threonine protein phosphatases may act as negative regulators of cellular growth. For example, treatment of cells with the tumor-promoter okadaic acid, an inhibitor of certain types of these phosphatases, resulted in the increased expression of several...
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Published in: | The Journal of biological chemistry Vol. 271; no. 11; pp. 5988 - 5992 |
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Main Authors: | , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
American Society for Biochemistry and Molecular Biology
15-03-1996
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Subjects: | |
Online Access: | Get full text |
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Summary: | Several lines of evidence indicate that serine/threonine protein phosphatases may act as negative regulators of cellular growth.
For example, treatment of cells with the tumor-promoter okadaic acid, an inhibitor of certain types of these phosphatases,
resulted in the increased expression of several proto-oncogenes, indicating a negative role of the respective phosphatases
in gene regulation. However, it was puzzling to find that okadaic acid-treated cells, even in the presence of highly expressed
proto-oncogenes, did not proliferate, but were arrested at certain points of the cell cycle. To further analyze this discrepancy,
we investigated the involvement of protein phosphatases in the control of other cell cycle regulatory genes, such as cdc2 , which encodes an essential cell cycle regulatory kinase. We found that cdc2 gene expression was blocked by okadaic acid, but stimulated by protein phosphatase 2A. Protein phosphatase 2A is shown to
be a positive regulator of cdc2 gene activity and to be required for cdc2 expression. Thus, our findings identify protein phosphatase 2A as a positive regulator of a major cell cycle regulatory gene
and therefore suggest a stimulatory role of this enzyme in this aspect of cellular growth control. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.271.11.5988 |