The impact of local genomic properties on the evolutionary fate of genes

Elife. 2023 May 24:12:e82290. doi: 10.7554/eLife.82290.

Abstract

Functionally indispensable genes are likely to be retained and otherwise to be lost during evolution. This evolutionary fate of a gene can also be affected by factors independent of gene dispensability, including the mutability of genomic positions, but such features have not been examined well. To uncover the genomic features associated with gene loss, we investigated the characteristics of genomic regions where genes have been independently lost in multiple lineages. With a comprehensive scan of gene phylogenies of vertebrates with a careful inspection of evolutionary gene losses, we identified 813 human genes whose orthologs were lost in multiple mammalian lineages: designated 'elusive genes.' These elusive genes were located in genomic regions with rapid nucleotide substitution, high GC content, and high gene density. A comparison of the orthologous regions of such elusive genes across vertebrates revealed that these features had been established before the radiation of the extant vertebrates approximately 500 million years ago. The association of human elusive genes with transcriptomic and epigenomic characteristics illuminated that the genomic regions containing such genes were subject to repressive transcriptional regulation. Thus, the heterogeneous genomic features driving gene fates toward loss have been in place and may sometimes have relaxed the functional indispensability of such genes. This study sheds light on the complex interplay between gene function and local genomic properties in shaping gene evolution that has persisted since the vertebrate ancestor.

Keywords: LAD; bamboo shark; central bearded dragon; chicken; chimpanzee; coelacanth; elusive gene; evolutionary biology; gene fate; gene loss; genetics; genomics; human; late replication timing; mouse; spotted gar; synonymous substitutions; tropical clawed flog.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Epigenomics*
  • Evolution, Molecular
  • Gene Expression Profiling
  • Genomics*
  • Humans
  • Mammals
  • Nucleotides

Substances

  • Nucleotides

Grants and funding

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.