Evolutionary Rate Heterogeneity and Functional Divergence of Orthologous Genes in Pyrus

Biomolecules. 2019 Sep 16;9(9):490. doi: 10.3390/biom9090490.

Abstract

Negatively selected genes (NSGs) and positively selected genes (PSGs) are the two types of most nuclear protein-coding genes in organisms. However, the evolutionary rates and characteristics of different types of genes have been rarely understood. In the present study, we investigate the rates of synonymous substitution (Ks) and the rates of non-synonymous substitution (Ka) by comparing the orthologous genes of two sequenced Pyrus species, Pyrus bretschneideri and Pyrus communis. Subsequently, we compared the evolutionary rates, gene structures, and expression profiles during different fruit development between PSGs and NSGs. Compared with the NSGs, the PSGs have fewer exons, shorter gene length, lower synonymous substitution rates and have higher evolutionary rates. Remarkably, gene expression patterns between two Pyrus species fruit indicated functional divergence for most of the orthologous genes derived from a common ancestor, and subfunctionalization for some of them. Overall, the present study shows that PSGs differs from NSGs not only under environmental selective pressure (Ka/Ks), but also in their structural, functional, and evolutionary properties. Additionally, our resulting data provides important insights for the evolution and highlights the diversification of orthologous genes in two Pyrus species.

Keywords: Pyrus; expression pattern; functional divergence; positive selection; selective modes.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Evolution, Molecular
  • Gene Expression Profiling / methods*
  • Gene Expression Regulation, Developmental
  • Gene Expression Regulation, Plant
  • Multigene Family*
  • Mutation Rate
  • Phylogeny
  • Plant Proteins / genetics
  • Plant Proteins / metabolism
  • Pyrus / classification
  • Pyrus / genetics
  • Pyrus / growth & development*
  • Selection, Genetic
  • Sequence Analysis, DNA / methods*
  • Silent Mutation

Substances

  • Plant Proteins