Low-fidelity DNA synthesis by human DNA polymerase theta

被引:119
作者
Arana, Mercedes E. [1 ,2 ]
Seki, Mineaki [3 ]
Wood, Richard D. [3 ]
Rogozin, Igor B. [4 ]
Kunkel, Thomas A. [1 ,2 ]
机构
[1] NIEHS, Mol Genet Lab, Natl Inst Hlth, Dept Hlth & Human Serv, Res Triangle Pk, NC 27709 USA
[2] NIEHS, Struct Biol Lab, Natl Inst Hlth, Dept Hlth & Human Serv, Res Triangle Pk, NC 27709 USA
[3] Univ Pittsburgh, Sch Med, Hillman Canc Ctr, Dept Pharmacol, Pittsburgh, PA 15213 USA
[4] Natl Lib Med, Natl Ctr Biotechnol Informat, Natl Inst Hlth, Dept Hlth & Human Serv, Bethesda, MD 20894 USA
关键词
D O I
10.1093/nar/gkn310
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human DNA polymerase theta (pol theta or POLQ) is a proofreading-deficient family A enzyme implicated in translesion synthesis (TLS) and perhaps in somatic hypermutation (SHM) of immunoglobulin genes. These proposed functions and kinetic studies imply that pol theta may synthesize DNA with low fidelity. Here, we show that when copying undamaged DNA, pol theta generates single base errors at rates 10- to more than 100-fold higher than for other family A members. Pol theta adds single nucleotides to homopolymeric runs at particularly high rates, exceeding 1% in certain sequence contexts, and generates single base substitutions at an average rate of 2.4 x 10(-3), comparable to inaccurate family Y human pol kappa (5.8 x 10(-3)) also implicated in TLS. Like pol kappa, pol theta is processive, implying that it may be tightly regulated to avoid deleterious mutagenesis. Pol theta also generates certain base substitutions at high rates within sequence contexts similar to those inferred to be copied by pol theta during SHM of immunoglobulin genes in mice. Thus, pol theta is an exception among family A polymerases, and its low fidelity is consistent with its proposed roles in TLS and SHM.
引用
收藏
页码:3847 / 3856
页数:10
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