The adaptive potential of circular DNA accumulation in ageing cells.

Curr Genet

Epigenetics Programme, The Babraham Institute, Cambridge, UK.

Published: October 2020

AI Article Synopsis

  • The stability of chromosomal DNA allows for long-term genetic consistency, but eukaryotic cells facing environmental stress can benefit from unstable circular DNA types, which lead to varied genetic traits.
  • Circular DNA, including forms like extrachromosomal circular DNA (eccDNA) and microDNA, is linked to drug resistance in cancer and pathogenic eukaryotes due to its non-Mendelian inheritance and high copy number variability.
  • In aging yeast, both ribosomal DNA-derived circular DNA and other protein-coding circular DNAs accumulate, enabling rapid adaptation to environmental changes while minimizing negative effects on younger populations.

Article Abstract

Carefully maintained and precisely inherited chromosomal DNA provides long-term genetic stability, but eukaryotic cells facing environmental challenges can benefit from the accumulation of less stable DNA species. Circular DNA molecules lacking centromeres segregate randomly or asymmetrically during cell division, following non-Mendelian inheritance patterns that result in high copy number instability and massive heterogeneity across populations. Such circular DNA species, variously known as extrachromosomal circular DNA (eccDNA), microDNA, double minutes or extrachromosomal DNA (ecDNA), are becoming recognised as a major source of the genetic variation exploited by cancer cells and pathogenic eukaryotes to acquire drug resistance. In budding yeast, circular DNA molecules derived from the ribosomal DNA (ERCs) have been long known to accumulate with age, but it is now clear that aged yeast also accumulate other high-copy protein-coding circular DNAs acquired through both random and environmentally-stimulated recombination processes. Here, we argue that accumulation of circular DNA provides a reservoir of heterogeneous genetic material that can allow rapid adaptation of aged cells to environmental insults, but avoids the negative fitness impacts on normal growth of unsolicited gene amplification in the young population.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7497353PMC
http://dx.doi.org/10.1007/s00294-020-01069-9DOI Listing

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