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Hypermutation in single-stranded DNA. | LitMetric

Hypermutation in single-stranded DNA.

DNA Repair (Amst)

Genome Integrity and Structural Biology Laboratory, National Institute of Environmental Health Sciences, US National Institutes of Health, Research Triangle Park, NC, USA. Electronic address:

Published: March 2021

AI Article Synopsis

  • * Persistent single-stranded DNA can lead to hypermutation, resulting in tightly-spaced clusters of mutations, which have been observed in both experimental models and cancer genomes.
  • * The review aims to summarize recent knowledge and developments regarding the mechanisms and causes of hypermutation in single-stranded DNA, including evidence from RNA viruses and the human germline.

Article Abstract

Regions of genomic DNA can become single-stranded in the course of normal replication and transcription as well as during DNA repair. Abnormal repair and replication intermediates can contain large stretches of persistent single-stranded DNA, which is extremely vulnerable to DNA damaging agents and hypermutation. Since such single-stranded DNA spans only a fraction of the genome at a given instance, hypermutation in these regions leads to tightly-spaced mutation clusters. This phenomenon of hypermutation in single-stranded DNA has been documented in several experimental models as well as in cancer genomes. Recently, hypermutated single-stranded RNA viral genomes also have been documented. Moreover, indications of hypermutation in single-stranded DNA may also be found in the human germline. This review will summarize key current knowledge and the recent developments in understanding the diverse mechanisms and sources of ssDNA hypermutation.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7234795PMC
http://dx.doi.org/10.1016/j.dnarep.2020.102868DOI Listing

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