Essential Roles for Polymerase θ-Mediated End Joining in the Repair of Chromosome Breaks.

ABSTRACT: DNA polymerase theta (Pol θ)-mediated end joining (TMEJ) has been implicated in the repair of chromosome breaks, but its cellular mechanism and role relative to canonical repair pathways are poorly understood. We show that it accounts for most repairs associated with microhomologies and is made efficient by coupling a microhomology search to removal of non-homologous tails and microhomology-primed synthesis across broken ends. In contrast to non-homologous end joining (NHEJ), TMEJ efficiently repairs end structures expected after aborted homology-directed repair (5' to 3' resected ends) or replication fork collapse. It typically does not compete with canonical repair pathways but, in NHEJ-deficient cells, is engaged more frequently and protects against translocation. Cell viability is also

SUBMITTER: Wyatt DW 

PROVIDER: S-EPMC4992412 | biostudies-literature | 2016 Aug

REPOSITORIES: biostudies-literature