AI Article Synopsis

  • Somatic mutations in the promoter region of the human telomerase reverse transcriptase gene are common in cancer, with the presence of G-quadruplex (G4) structures linked to higher mutagenicity and genome instability.
  • A bioinformatics analysis of 141 mammalian species revealed that G4 motifs are mostly found near the transcription start site and are prevalent on the non-coding strand, with a notable portion being evolutionarily conserved.
  • Additionally, a significant increase in nucleotide substitutions was observed in conserved G4 motifs compared to surrounding genomic regions, suggesting that G4s may hinder DNA repair and influence evolutionary adaptations.

Article Abstract

Somatic mutations in the promoter region of the human telomerase reverse transcriptase () gene have been identified in many types of cancer. The promoter is known to be enriched with sequences that enable the formation of G-quadruplex (G4) structures, whose presence is associated with elevated mutagenicity and genome instability. Here, we used a bioinformatics tool (QGRS mapper) to search for G4-forming sequences (G4 motifs) in the 1000 bp promoter regions of 141 mammalian species belonging to 20 orders, 5 of which, including primates and predators, contain more than 10 species. Groups of conserved G4 motifs and single-nucleotide variants within these groups were discovered using a block alignment approach (based on the Nucleotide PanGenome explorer). It has been shown that: (i) G4 motifs are predominantly located in the region proximal to the transcription start site (up to 400 bp) and are over-represented on the non-coding strand of the promoters, (ii) 11 to 22% of the G4 motifs found are evolutionarily conserved across the related organisms, and (iii) a statistically significant higher frequency of nucleotide substitutions in the conserved G4 motifs compared to the surrounding regions was confirmed only for the order . These data support the assumption that G4s can interfere with the DNA repair process and affect the evolutionary adaptation of organisms and species.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10381784PMC
http://dx.doi.org/10.3390/life13071478DOI Listing

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