APOBEC Mutagenesis is Low in Most Types of Non-B DNA Structures
Overview
Authors
Affiliations
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, owing to the depletion of their mutational signature motifs.
Structural underpinnings of mutation rate variations in the human genome.
Liu Z, Hassan Samee M Nucleic Acids Res. 2023; 51(14):7184-7197.
PMID: 37395403 PMC: 10415140. DOI: 10.1093/nar/gkad551.
Inverted repeats in the monkeypox virus genome are hot spots for mutation.
Dobrovolna M, Brazda V, Warner E, Bidula S J Med Virol. 2022; 95(1):e28322.
PMID: 36400742 PMC: 10100261. DOI: 10.1002/jmv.28322.