PLoS Biology (Nov 2006)

A role for PCNA ubiquitination in immunoglobulin hypermutation.

  • Hiroshi Arakawa,
  • George-Lucian Moldovan,
  • Huseyin Saribasak,
  • Nesibe Nur Saribasak,
  • Stefan Jentsch,
  • Jean-Marie Buerstedde

DOI
https://doi.org/10.1371/journal.pbio.0040366
Journal volume & issue
Vol. 4, no. 11
p. e366

Abstract

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Proliferating cell nuclear antigen (PCNA) is a DNA polymerase cofactor and regulator of replication-linked functions. Upon DNA damage, yeast and vertebrate PCNA is modified at the conserved lysine K164 by ubiquitin, which mediates error-prone replication across lesions via translesion polymerases. We investigated the role of PCNA ubiquitination in variants of the DT40 B cell line that are mutant in K164 of PCNA or in Rad18, which is involved in PCNA ubiquitination. Remarkably, the PCNA(K164R) mutation not only renders cells sensitive to DNA-damaging agents, but also strongly reduces activation induced deaminase-dependent single-nucleotide substitutions in the immunoglobulin light-chain locus. This is the first evidence, to our knowledge, that vertebrates exploit the PCNA-ubiquitin pathway for immunoglobulin hypermutation, most likely through the recruitment of error-prone DNA polymerases.