DNA Copy Number Variations as Markers of Mutagenic Impact

Int J Mol Sci. 2019 Sep 24;20(19):4723. doi: 10.3390/ijms20194723.

Abstract

DNA copy number variation (CNV) occurs due to deletion or duplication of DNA segments resulting in a different number of copies of a specific DNA-stretch on homologous chromosomes. Implications of CNVs in evolution and development of different diseases have been demonstrated although contribution of environmental factors, such as mutagens, in the origin of CNVs, is poorly understood. In this review, we summarize current knowledge about mutagen-induced CNVs in human, animal and plant cells. Differences in CNV frequencies induced by radiation and chemical mutagens, distribution of CNVs in the genome, as well as adaptive effects in plants, are discussed. Currently available information concerning impact of mutagens in induction of CNVs in germ cells is presented. Moreover, the potential of CNVs as a new endpoint in mutagenicity test-systems is discussed.

Keywords: animal and plant cells; chemical mutagens; copy number variation; human; radiation.

Publication types

  • Review

MeSH terms

  • Animals
  • Breeding
  • DNA Copy Number Variations* / drug effects
  • DNA Copy Number Variations* / radiation effects
  • Evolution, Molecular
  • Germ-Line Mutation / drug effects
  • Germ-Line Mutation / radiation effects
  • Humans
  • Mutagenesis* / drug effects
  • Mutagenesis* / radiation effects
  • Mutagens / pharmacology
  • Mutagens / toxicity
  • Plants / genetics
  • Radiation, Ionizing

Substances

  • Mutagens