a National Center for Biotechnology Information, National Library of Medicine , National Institutes of Health , Bethesda , MD , USA.
b Department Microbiology and Molecular Genetics , University of California , Davis , CA , USA.
Cell Cycle. 2018;17(3):348-355. doi: 10.1080/15384101.2017.1404208. Epub 2018 Feb 15.
DNA polymerase (pol) η is a specialized error-prone polymerase with at least two quite different and contrasting cellular roles: to mitigate the genetic consequences of solar UV irradiation, and promote somatic hypermutation in the variable regions of immunoglobulin genes. Misregulation and mistargeting of pol η can compromise genome integrity. We explored whether the mutational signature of pol η could be found in datasets of human somatic mutations derived from normal and cancer cells. A substantial excess of single and tandem somatic mutations within known pol η mutable motifs was noted in skin cancer as well as in many other types of human cancer, suggesting that somatic mutations in A:T bases generated by DNA polymerase η are a common feature of tumorigenesis. Another peculiarity of pol ηmutational signatures, mutations in YCG motifs, led us to speculate that error-prone DNA synthesis opposite methylated CpG dinucleotides by misregulated pol η in tumors might constitute an additional mechanism of cytosine demethylation in this hypermutable dinucleotide.
DNA 聚合酶(pol)η 是一种具有至少两种截然不同和对比鲜明的细胞作用的专门易错聚合酶:减轻太阳紫外线照射的遗传后果,并促进免疫球蛋白基因可变区的体细胞超突变。pol η 的失调和靶向错误会损害基因组完整性。我们探讨了 pol η 的突变特征是否可以在源自正常和癌细胞的人类体细胞突变数据集。在皮肤癌以及许多其他类型的人类癌症中,在已知的 pol η 易变基序内的单碱基和串联体细胞突变明显过多,这表明由 DNA 聚合酶 η 产生的 A:T 碱基的体细胞突变是肿瘤发生的一个常见特征。pol η 突变特征的另一个特殊性,即 YCG 基序中的突变,使我们推测,在肿瘤中,错误调节的 pol η 对甲基化 CpG 二核苷酸进行易错 DNA 合成可能构成这种超突变二核苷酸中胞嘧啶去甲基化的另一种机制。