4.7 Article

DNA Replication-Coupled PCNA Mono-Ubiquitination and Polymerase Switching in a Human In Vitro System

Journal

JOURNAL OF MOLECULAR BIOLOGY
Volume 396, Issue 3, Pages 487-500

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jmb.2010.01.003

Keywords

DNA polymerase switching; DNA replication; PCNA mono-ubiquitination; translesion DNA synthesis

Funding

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan
  2. Health and Labour Science Research Grants
  3. Ministry of Health, Labour and Welfare
  4. Radiation Effects Association
  5. Japan Society for the Promotion of Science

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Translesion DNA synthesis is a mechanism of DNA damage tolerance, and mono-ubiquitination of proliferating cell nuclear antigen (PCNA) is considered to play a key role in regulating the switch from replicative to translesion DNA polymerases (pols). In this study, we analyzed effects of a replicative pol delta on PCNA mono-ubiquitination with the ubiquitin-conjugating enzyme and ligase UBE2A/HHR6A/RAD6A-RAD18. The results revealed that PCNA interacting with pol 8 is a better target for ubiquitination, and PCNA mono-ubiquitination could be coupled with DNA replication. Consequently, we could reconstitute replication-coupled switching between pol delta and a translesion pol, pol eta, on an ultraviolet-light-irradiated template. With this system, we obtained direct evidence that polymerase switching reactions are stimulated by mono-ubiquitination of PCNA, depending on a function of the ubiquitin binding zinc finger domain of pol eta. This study provides a framework for detailed analyses of molecular mechanisms of human pol switching and regulation of translesion DNA synthesis. (C) 2010 Elsevier Ltd. All rights reserved.

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