| Literature DB >> 29139326 |
Igor B Rogozin1, Alexander Goncearenco1, Artem G Lada2, Subhajyoti De3, Vyacheslav Yurchenko4, German Nudelman5, Anna R Panchenko1, David N Cooper6, Youri I Pavlov7,8,9,10.
Abstract
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.Entities:
Keywords: DNA lesion bypass; Hypermutation; POLH; gene expression profiles; mutable motif; skin cancer; sloppy DNA polymerase
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Year: 2018 PMID: 29139326 PMCID: PMC5914734 DOI: 10.1080/15384101.2017.1404208
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534