Compared to other NHEJ factors, DNA-PK protein and RNA levels are markedly increased in all higher primates, but not in prosimians or other mammals

DNA Repair (Amst). 2024 Oct:142:103737. doi: 10.1016/j.dnarep.2024.103737. Epub 2024 Aug 8.

Abstract

The DNA dependent protein kinase (DNA-PK) initiates non-homologous recombination (NHEJ), the predominate DNA double-strand break (DSBR) pathway in higher vertebrates. It has been known for decades that the enzymatic activity of DNA-PK [that requires its three component polypeptides, Ku70, Ku80 (that comprise the DNA-end binding Ku heterodimer), and the catalytic subunit (DNA-PKcs)] is present in humans at 10-50 times the level observed in other mammals. Here, we show that the high level of DNA-PKcs protein expression appears evolutionarily in mammals between prosimians and higher primates. Moreover, the RNAs encoding the three component polypeptides of DNA-PK are present at similarly high levels in hominids, new-, and old-world monkeys, but expression of these RNAs in prosimians is ∼5-50 fold less, analogous to the levels observed in other non-primate species. This is reminiscent of the appearance of Alu repeats in primate genomes -- abundant in higher primates, but present at much lower density in prosimians. Alu repeats are well-known for their capacity to promote non-allelic homologous recombination (NAHR) a process known to be inhibited by DNA-PK. Nanopore sequence analyses of cultured cells proficient or deficient in DNA-PK revealed an increase of inter-chromosomal translocations caused by NAHR. Although the high levels of DNA-PK in primates may have many functions, we posit that high levels of DNA-PK may function to restrain deleterious NAHR events between Alu elements.

Keywords: DNA dependent protein kinase (DNA-PK); DNA-PK catalytic subunit (DNA-PKcs); Non-allelic homologous recombination (NAHR); Non-homologous end joining (NHEJ).

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • DNA Breaks, Double-Stranded
  • DNA End-Joining Repair*
  • DNA-Activated Protein Kinase* / genetics
  • DNA-Activated Protein Kinase* / metabolism
  • Evolution, Molecular
  • Humans
  • Ku Autoantigen / genetics
  • Ku Autoantigen / metabolism
  • Mammals / genetics
  • Mammals / metabolism
  • Primates* / genetics
  • Primates* / metabolism
  • RNA / metabolism

Substances

  • DNA-Activated Protein Kinase
  • Ku Autoantigen
  • RNA