| First Author | Pryor JM | Year | 2015 |
| Journal | Proc Natl Acad Sci U S A | Volume | 112 |
| Issue | 33 | Pages | E4537-45 |
| PubMed ID | 26240371 | Mgi Jnum | J:226560 |
| Mgi Id | MGI:5697760 | Doi | 10.1073/pnas.1505805112 |
| Citation | Pryor JM, et al. (2015) Essential role for polymerase specialization in cellular nonhomologous end joining. Proc Natl Acad Sci U S A 112(33):E4537-45 |
| abstractText | Nonhomologous end joining (NHEJ) repairs chromosome breaks and must remain effective in the face of extensive diversity in broken end structures. We show here that this flexibility is often reliant on the ability to direct DNA synthesis across strand breaks, and that polymerase (Pol) mu and Pol lambda are the only mammalian DNA polymerases that have this activity. By systematically varying substrate in cells, we show each polymerase is uniquely proficient in different contexts. The templating nucleotide is also selected differently, with Pol mu using the unpaired base adjacent to the downstream 5' phosphate even when there are available template sites further upstream of this position; this makes Pol mu more flexible but also less accurate than Pol lambda. Loss of either polymerase alone consequently has clear and distinguishable effects on the fidelity of repair, but end remodeling by cellular nucleases and the remaining polymerase helps mitigate the effects on overall repair efficiency. Accordingly, when cells are deficient in both polymerases there is synergistic impact on NHEJ efficiency, both in terms of repair of defined substrates and cellular resistance to ionizing radiation. Pol mu and Pol lambda thus provide distinct solutions to a problem for DNA synthesis that is unique to this pathway and play a key role in conferring on NHEJ the flexibility required for accurate and efficient repair. |
