| Literature DB >> 11599922 |
K J Cheung1, G Li.
Abstract
The regulation of Chk1, a critical protein kinase involved in G(2) phase arrest, has been a subject of recent research. Chk1 phosphorylates tumor suppressor p53 at multiple sites, while p53 has been shown to downregulate Chk1 expression under stress conditions in vitro, suggesting negative feedback between the two checkpoint proteins. Using the p53 knockout mouse model, we demonstrate by Western blot and immunohistochemistry that mChk1 expression is induced in spleen, thymus, and dermal fibroblasts and is reduced in lung and testis in p53(-/-) mice compared to p53(+/+) controls. The mChk1 protein was undetectable in heart, kidney, and skin, whereas abundant expression was observed in brain and liver in both p53(+/+) and p53(-/-) mice. These data indicate that p53 regulates Chk1 expression in a tissue-specific manner. Copyright 2001 Academic Press.Entities:
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Year: 2001 PMID: 11599922 DOI: 10.1006/exmp.2001.2398
Source DB: PubMed Journal: Exp Mol Pathol ISSN: 0014-4800 Impact factor: 3.362