DNA polymerase POLQ and cellular defense against DNA damage

Matthew J. Yousefzadeh, Richard D. Wood

Research output: Contribution to journalReview articlepeer-review

79 Scopus citations


In mammalian cells, POLQ (pol θ) is an unusual specialized DNA polymerase whose in vivo function is under active investigation. POLQ has been implicated by different experiments to play a role in resistance to ionizing radiation and defense against genomic instability, in base excision repair, and in immunological diversification. The protein is formed by an N-terminal helicase-like domain, a C-terminal DNA polymerase domain, and a large central domain that spans between the two. This arrangement is also found in the Drosophila Mus308 protein, which functions in resistance to DNA interstrand crosslinking agents. Homologs of POLQ and Mus308 are found in multicellular eukaryotes, including plants, but a comparison of phenotypes suggests that not all of these genes are functional orthologs. Flies defective in Mus308 are sensitive to DNA interstrand crosslinking agents, while mammalian cells defective in POLQ are primarily sensitive to DNA double-strand breaking agents. Cells from Polq-/- mice are hypersensitive to radiation and peripheral blood cells display increased spontaneous and ionizing radiation-induced levels of micronuclei (a hallmark of gross chromosomal aberrations), though mice apparently develop normally. Loss of POLQ in human and mouse cells causes sensitivity to ionizing radiation and other double strand breaking agents and increased DNA damage signaling. Retrospective studies of clinical samples show that higher levels of POLQ gene expression in breast and colorectal cancer are correlated with poorer outcomes for patients. A clear understanding of the mechanism of action and physiologic function of POLQ in the cell is likely to bear clinical relevance.

Original languageEnglish (US)
Pages (from-to)1-9
Number of pages9
JournalDNA Repair
Issue number1
StatePublished - Jan 1 2013
Externally publishedYes

Bibliographical note

Funding Information:
We thank Kei-ichi Takata, Francesca Cole, and Sylvie Doublié for helpful comments on the manuscript. This research was supported by NIH Training Grant T32 CA09480 , Grant P01 CA09717 from the National Cancer Institute and by NIH Cancer Center Support Grant P30-CA016672 (University of Texas M.D. Anderson Cancer Center).


  • Abasic site
  • DNA polymerase
  • Genomic instability
  • Ionizing radiation
  • POLQ
  • Thymine glycol
  • Translesion synthesis


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