PCNA: structure, functions and interactions (original) (raw)

Oncogene volume 14, pages 629–640 (1997)Cite this article

Abstract

Proliferating cell nuclear antigen (PCNA) plays an essential role in nucleic acid metabolism as a component of the replication and repair machinery. This toroidal-shaped protein encircles DNA and can slide bi-directionally along the duplex. One of the well-established functions for PCNA is its role as the processivity factor for DNA polymerase δ and ε. PCNA tethers the polymerase catalytic unit to the DNA template for rapid and processive DNA synthesis. In the last several years it has become apparent that PCNA interacts with proteins involved in cell-cycle progression which are not a part of the DNA polymerase apparatus. Some of these interactions have a direct effect on DNA synthesis while the roles of several other interactions are not fully understood. This review summarizes the structural features of PCNA and describes the diverse functions played by the protein in DNA replication and repair as well as its possible role in chromatin assembly and gene transcription. The PCNA interactions with different cellular proteins and the importance of these interactions are also discussed.

This is a preview of subscription content, access via your institution

Access options

Subscribe to this journal

Receive 50 print issues and online access

$259.00 per year

only $5.18 per issue

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Additional access options:

Similar content being viewed by others

Author information

Authors and Affiliations

  1. Department of Molecular Biology and Genetics, Johns Hopkins School of Medicine, 725 N Wolfe Street, Baltimore, Maryland, 21205, USA
    Zvi Kelman

Authors

  1. Zvi Kelman
    You can also search for this author inPubMed Google Scholar

Rights and permissions

About this article

Cite this article

Kelman, Z. PCNA: structure, functions and interactions.Oncogene 14, 629–640 (1997). https://doi.org/10.1038/sj.onc.1200886

Download citation

Keywords

This article is cited by