Modes of gene duplication contribute differently to genetic novelty and redundancy, but show parallels across divergent angiosperms

PLoS One. 2011;6(12):e28150. doi: 10.1371/journal.pone.0028150. Epub 2011 Dec 2.

Abstract

Background: Both single gene and whole genome duplications (WGD) have recurred in angiosperm evolution. However, the evolutionary effects of different modes of gene duplication, especially regarding their contributions to genetic novelty or redundancy, have been inadequately explored.

Results: In Arabidopsis thaliana and Oryza sativa (rice), species that deeply sample botanical diversity and for which expression data are available from a wide range of tissues and physiological conditions, we have compared expression divergence between genes duplicated by six different mechanisms (WGD, tandem, proximal, DNA based transposed, retrotransposed and dispersed), and between positional orthologs. Both neo-functionalization and genetic redundancy appear to contribute to retention of duplicate genes. Genes resulting from WGD and tandem duplications diverge slowest in both coding sequences and gene expression, and contribute most to genetic redundancy, while other duplication modes contribute more to evolutionary novelty. WGD duplicates may more frequently be retained due to dosage amplification, while inferred transposon mediated gene duplications tend to reduce gene expression levels. The extent of expression divergence between duplicates is discernibly related to duplication modes, different WGD events, amino acid divergence, and putatively neutral divergence (time), but the contribution of each factor is heterogeneous among duplication modes. Gene loss may retard inter-species expression divergence. Members of different gene families may have non-random patterns of origin that are similar in Arabidopsis and rice, suggesting the action of pan-taxon principles of molecular evolution.

Conclusion: Gene duplication modes differ in contribution to genetic novelty and redundancy, but show some parallels in taxa separated by hundreds of millions of years of evolution.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Algorithms
  • Arabidopsis / genetics
  • Biological Evolution
  • Conserved Sequence
  • DNA Methylation
  • Gene Duplication*
  • Gene Expression Regulation, Plant*
  • Genes, Plant
  • Genetic Variation
  • Magnoliopsida / genetics*
  • Magnoliopsida / physiology
  • Models, Genetic
  • Oryza / genetics
  • Plant Physiological Phenomena
  • Promoter Regions, Genetic
  • Regression Analysis
  • Sequence Analysis, DNA