1. APOBEC mutagenesis is low in most types of non-B DNA structures, unlike other types of cancer mutagenesis
- Author
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Nina-Vicky Landik, Ruslan Abasov, Mikhail S. Gelfand, Bulat Fatykhov, Alexandra A. Denisova, Almira Chervova, Gennady V. Ponomarev, Vladimir A. Nazarov, Evgeny Shvarov, and Marat D. Kazanov
- Subjects
Genetics ,APOBEC ,chemistry.chemical_compound ,Mutation ,Chemistry ,Inverted repeat ,Mutagenesis ,medicine ,Direct repeat ,medicine.disease_cause ,Genome ,Cytosine ,DNA - Abstract
While somatic mutations are known to be enriched in genome regions with non-canonical DNA secondary structure, the impact of particular mutagens still needs to be elucidated. Here, we demonstrate that in human cancers, the APOBEC mutagenesis is not enriched in direct repeats, mirror repeats, short tandem repeats, and G-quadruplexes, and even decreased below its level in B-DNA for cancer samples with very high APOBEC activity. In contrast, we observe that the APOBEC-induced mutational density is positively associated with APOBEC activity in inverted repeats (cruciform structures), where the impact of cytosine at the 3’-end of the hairpin loop is substantial. Surprisingly, the APOBEC-signature mutation density per TC motif in the single-stranded DNA of a G-quadruplex (G4) is lower than in the four-stranded part of G4 and in B-DNA. The APOBEC mutagenesis, as well as the UV-mutagenesis in melanoma samples are absent in Z-DNA regions, due to depletion of their mutational signature motifs.
- Published
- 2021