doi:10.1016/S0169-5347(99)01638-9
Copyright © 1999 Elsevier Science Ltd. All rights reserved.
Review
Polyploidy: recurrent formation and genome evolution
Douglas E. Soltis
and Pamela S. Soltis
Dept of Botany, Washington State University, Pullman, WA 99164, USA
Available online 17 August 1999.
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Abstract
Polyploidy has played a major role in the evolution of many eukaryotes. Recent studies have dramatically reshaped views of polyploid evolution, demonstrating that most polyploid species examined, both plant and animal, have formed recurrently from different populations of their progenitors. Populations of independent origin can subsequently come into contact and hybridize, generating new genotypes. Because of the frequency of polyploidy in plants, many recognized species are probably polyphyletic. Extensive and rapid genome restructuring can occur after polyploidization. Such changes can be mediated by transposons. Polyploidization could represent a period of transilience, during which genomic changes occur, potentially producing new gene complexes and facilitating rapid evolution.
Author Keywords: Polyploidy; Recurrent species formation; Genome restructuring; Transilience; Transposable elements; Diploidizationa
Subject-index terms: Evolution; Genetics
Fig. 1. Comparison of (a) traditional view of polyploid formation with (b) new or revised view. The traditional view envisioned each polyploid species forming only once, resulting in a new species that was genetically uniform (or nearly so). The new view suggests that each polyploid species forms over and over again from different parental genotypes generating a diverse array of polyploid genotypes. Subsequent hybridization among these polyploid genotypes and recombination result in additional genetic variability.
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Fig .2. Comparison of (a) traditional view of genomic evolution subsequent to polyploid formation with (b) new or revised view. The classic view of genome evolution suggested that interactions between the parental genomes of an allopolyploid were minimal. Recently, it has become apparent that both intra- as well as inter-genomic rearrangements occur. (b) In this example, arrows indicate genomic rearrangements – intragenomic rearrangements are represented by hatched areas on chromosomes from ‘diploid B’; intergenomic rearrangements are represented by translocation of ‘black’ or ‘white’ chromosomal segments between the genomes of ‘diploid A’ and ‘diploid B’. The degree of genomic change can also be influenced by cytoplasmic–nuclear interactions. In a newly formed allopolyploid, there are adverse interactions between the nuclear genome contributed by the male parental diploid and both the nuclear and cytoplasmic genomes of the female parental diploid; genome adjustments must occur to restore nuclear–cytoplasmic compatibility. Available data suggest that the nuclear genome of maternal origin experiences less change than does the paternal nuclear genome. Other evidence implicates transposable elements in the genome reorganization that has been detected in polyploids.