Citation

  • Authors: Capp, J. P., Boudsocq, F., Bertrand, P., Laroche-Clary, A., Pourquier, P., Lopez, B. S., Cazaux, C., Hoffmann, J. S., Canitrot, Y.
  • Year: 2006
  • Journal: Nucleic Acids Res 34 2998-3007
  • Applications: in vitro / DNA / jetPEI
  • Cell type: CHO-DRA10

Abstract

DNA polymerase lambda (pollambda) is a recently identified DNA polymerase whose cellular function remains elusive. Here we show, that pollambda participates at the molecular level in a chromosomal context, in the repair of DNA double strand breaks (DSB) via non-homologous end joining (NHEJ) in mammalian cells. The expression of a catalytically inactive form of pollambda (pollambdaDN) decreases the frequency of NHEJ events in response to I-Sce-I-induced DSB whereas inactivated forms of its homologues polbeta and polmu do not. Only events requiring DNA end processing before ligation are affected; this defect is associated with large deletions arising in the vicinity of the induced DSB. Furthermore, pollambdaDN-expressing cells exhibit increased sensitization and genomic instability in response to ionizing radiation similar to that of NHEJ-defective cells. Our data support a requirement for pollambda in repairing a subset of DSB in genomic DNA, thereby contributing to the maintenance of genetic stability mediated by the NHEJ pathway.

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