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THE P21 INHIBITOR OF CYCLIN-DEPENDENT KINASES CONTROLS DNA-REPLICATION BY INTERACTION WITH PCNA
Author(s): WAGA S, HANNON GJ, BEACH D, STILLMAN B
Source: NATURE    Volume: 369    Issue: 6481    Pages: 574-578    Published: JUN 16 1994  
Times Cited: 1,317     References: 29     
Abstract: THE p53 tumour-suppressor protein controls the expression of a gene encoding the p21 cyclin-dependent protein kinase (CDK) regulator(1-6). Levels of p21 protein are increased in senescent cells and p21 overexpression blocks the growth of tumour cells(1,3,7). In normal human cells, but not in many tumour cells, p21 exists in a guaternary complex with a cyclin, a CDK, and the proliferating-cell nuclear antigen (PCNA)(5,8). p21 controls CDK activity, thereby affecting cell-cycle control(2-4,6), whereas PCNA functions in both DNA replication(9-12) and repair(13). Here we use simian virus 40 DNA replication in vitro to show that p21 directly inhibits PCNA-dependent DNA replication in the absence of a cyclin/CDK. Furthermore, p21 blocks the ability of PCNA to activate DNA polymerase delta, the principal replicative DNA polymerase. This regulation results from a direct interaction between p21 and PCNA. Thus, during p53-mediated suppression of cell proliferation, p21 and PCNA mag be important for coordinating cell-cycle progression, DNA replication and repair of damaged DNA.
Document Type: Article
Language: English
Reprint Address: WAGA, S (reprint author), COLD SPRING HARBOR LAB, POB 100, BUNGTOWN RD, COLD SPRING HARBOR, NY 11724 USA
Addresses:
1. HOWARD HUGHES MED INST, COLD SPRING HARBOR, NY 11724 USA
Publisher: MACMILLAN MAGAZINES LTD, PORTERS SOUTH, 4 CRINAN ST, LONDON, ENGLAND N1 9XW
Subject Category: Multidisciplinary Sciences
IDS Number: NR294
ISSN: 0028-0836
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