Natural pathways towards polyploidy in animals: the Squalius alburnoides fish complex as a model system to study genome size and genome reorganization in polyploids
- PMID: 23796598
- DOI: 10.1159/000351729
Natural pathways towards polyploidy in animals: the Squalius alburnoides fish complex as a model system to study genome size and genome reorganization in polyploids
Abstract
When comparing the known picture of polyploidy in animals and in plants, it is possible to recognize some similarities, namely: (i) multiple and recurrent origins in several well-established taxonomic groups; (ii) a strong and regular association with hybridization events; (iii) the production of genotypic diversity; (iv) a rapid genomic reshuffling; (v) a very active role of transposable elements in allopolyploids; (vi) a comparatively privileged occurrence in harsher environments when compared with their diploid relatives, and (vii) gene silencing and divergence of duplicated genes without disruption of duplicated loci. Research on polyploidy was highly biased towards plants during the last century because polyploidy in animals was for long time considered rare, occasional and irrelevant from an evolutionary perspective. However, as empirically observed in plants, genome rediploidization starts in polyploid organisms immediately after the polyploid shock. Given the speed and dynamicity of this process, evidence of genome multiplication is completely erased over time, and hence, only the most recent events are likely to be acknowledged. Although varying in expression between and within taxonomic groups, polyploidy and hybridization are ubiquitous in animals and may be recurrent, fostering evolution. Since evolutionary allopolyploid genomes behave as biologically diploid, zoologists have to challenge the old paradigm of an irrelevant evolutionary role in animals using current genomic and cytogenomic tools. These methods are most likely to reveal the role of polyploid mechanisms in producing evolutionary novelties. Nonsexual complexes are the perfect models to bridge the gap between empirical and theoretical research, while the evolutionary process is in action. Such animal complexes represent a transient stage that, in general, moves towards a polyploid stage, where bisexuality might be recovered, ultimately giving rise to a new gonochoric species. These pathways are herein illustrated by the Iberian allopolyploid Squalius alburnoides. Some general aspects on this fish's complex are updated and reviewed, namely the reproductive modes of the distinct genomotypes, since variable ploidies and genomic combinations occur in natural populations. Most recent data on the mechanisms of gene expression regulation and the importance of the genomic context in driving allelic expression are also included. It was first demonstrated that a regulatory mechanism involving dosage compensation by gene-copy silencing exists in allotriploid females and that allelic expression patterns differed either between genomically equivalent individuals or within the same individual (between tissues and genes). Thus, instead of a whole haplome inactivation, a biased silencing towards repression of a specific allele was observed as well as a reduction of the transcript levels to the diploid state. See also sister article focusing on plants by Tayalé and Parisod in this themed issue.
Copyright © 2013 S. Karger AG, Basel.
Similar articles
-
Dosage compensation by gene-copy silencing in a triploid hybrid fish.Curr Biol. 2008 Sep 9;18(17):1344-8. doi: 10.1016/j.cub.2008.07.096. Curr Biol. 2008. PMID: 18771921
-
Natural pathways to polyploidy in plants and consequences for genome reorganization.Cytogenet Genome Res. 2013;140(2-4):79-96. doi: 10.1159/000351318. Epub 2013 Jun 8. Cytogenet Genome Res. 2013. PMID: 23751271 Review.
-
Gene copy silencing and DNA methylation in natural and artificially produced allopolyploid fish.J Exp Biol. 2016 Oct 1;219(Pt 19):3072-3081. doi: 10.1242/jeb.140418. Epub 2016 Jul 21. J Exp Biol. 2016. PMID: 27445349
-
Genetic and genomic interactions of animals with different ploidy levels.Cytogenet Genome Res. 2013;140(2-4):117-36. doi: 10.1159/000351593. Epub 2013 Jun 8. Cytogenet Genome Res. 2013. PMID: 23751376 Review.
-
Gene expression dosage regulation in an allopolyploid fish.PLoS One. 2015 Mar 19;10(3):e0116309. doi: 10.1371/journal.pone.0116309. eCollection 2015. PLoS One. 2015. PMID: 25789776 Free PMC article.
Cited by
-
Uniparental Genome Elimination in Australian Carp Gudgeons.Genome Biol Evol. 2021 Jun 8;13(6):evab030. doi: 10.1093/gbe/evab030. Genome Biol Evol. 2021. PMID: 33591327 Free PMC article.
-
Epigenetic control of mobile DNA as an interface between experience and genome change.Front Genet. 2014 Apr 25;5:87. doi: 10.3389/fgene.2014.00087. eCollection 2014. Front Genet. 2014. PMID: 24795749 Free PMC article. Review.
-
Mobile Elements in Ray-Finned Fish Genomes.Life (Basel). 2020 Sep 25;10(10):221. doi: 10.3390/life10100221. Life (Basel). 2020. PMID: 32992841 Free PMC article. Review.
-
Clonal reproduction assured by sister chromosome pairing in dojo loach, a teleost fish.Chromosome Res. 2018 Dec;26(4):243-253. doi: 10.1007/s10577-018-9581-4. Epub 2018 Jun 7. Chromosome Res. 2018. PMID: 29882067
-
Profound genetic divergence and asymmetric parental genome contributions as hallmarks of hybrid speciation in polyploid toads.Proc Biol Sci. 2018 Feb 14;285(1872):20172667. doi: 10.1098/rspb.2017.2667. Epub 2018 Feb 7. Proc Biol Sci. 2018. PMID: 29436499 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous