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酵母DNA聚合酶ζ介导的核糖核苷酸掺入

Ribonucleotide incorporation by yeast DNA polymerase ζ.

作者信息

Makarova Alena V, Nick McElhinny Stephanie A, Watts Brian E, Kunkel Thomas A, Burgers Peter M

机构信息

Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, MO 63110, USA.

Laboratory of Molecular Genetics and Laboratory of Structural Biology, National Institute of Environmental Health Sciences, National Institutes of Health, Department of Health and Human Services, Research Triangle Park, NC 27709, USA.

出版信息

DNA Repair (Amst). 2014 Jun;18:63-7. doi: 10.1016/j.dnarep.2014.02.017. Epub 2014 Mar 24.

Abstract

During replication in yeast, the three B family DNA replicases frequently incorporate ribonucleotides (rNMPs) into DNA, and their presence in the nuclear genome can affect genome stability. This prompted us to examine ribonucleotide incorporation by the fourth B family member, Pol ζ, the enzyme responsible for the majority of damage-induced mutagenesis in eukaryotes. We first show that Pol ζ inserts rNMPs into DNA and can extend primer termini containing 3'-ribonucleotides. We then measure rNMP incorporation by Pol ζ in the presence of its cofactors, RPA, RFC and PCNA and at normal cellular dNTP and rNTP concentrations that exist under unstressed conditions. Under these conditions, Pol ζ stably incorporates one rNMP for every 200-300 dNMPs incorporated, a frequency that is slightly higher than for the high fidelity replicative DNA polymerases. Under damage-induced conditions wherein cellular dNTP concentrations are elevated 5-fold, Pol ζ only incorporates one rNMP per 1300 dNMPs. Functional interaction of Pol ζ with the mutasome assembly factor Rev1 gives comparable rNMP incorporation frequencies. These results suggest that ribonucleotide incorporation into DNA during Pol ζ-mediated mutagenesis in vivo may be rare.

摘要

在酵母复制过程中,三种B家族DNA复制酶经常将核糖核苷酸(rNMPs)掺入DNA,它们在核基因组中的存在会影响基因组稳定性。这促使我们研究第四个B家族成员Pol ζ的核糖核苷酸掺入情况,该酶负责真核生物中大部分损伤诱导的诱变。我们首先表明,Pol ζ将rNMPs插入DNA,并能延伸含有3'-核糖核苷酸的引物末端。然后,我们在其辅因子RPA、RFC和PCNA存在的情况下,以及在未受应激条件下正常细胞dNTP和rNTP浓度下,测量Pol ζ的rNMP掺入情况。在这些条件下,Pol ζ每掺入200 - 300个dNMPs就稳定地掺入一个rNMP,这一频率略高于高保真复制性DNA聚合酶。在损伤诱导条件下,细胞dNTP浓度升高5倍,Pol ζ每掺入1300个dNMPs才掺入一个rNMP。Pol ζ与诱变体组装因子Rev1的功能相互作用产生了相当的rNMP掺入频率。这些结果表明,在体内Pol ζ介导的诱变过程中,核糖核苷酸掺入DNA的情况可能很少见。

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