» Articles » PMID: 24958924

Polyploidy and Novelty: Gottlieb's Legacy

Overview
Specialty Biology
Date 2014 Jun 25
PMID 24958924
Citations 63
Authors
Affiliations
Soon will be listed here.
Abstract

Nearly four decades ago, Roose & Gottlieb (Roose & Gottlieb 1976 Evolution 30, 818-830. (doi:10.2307/2407821)) showed that the recently derived allotetraploids Tragopogon mirus and T. miscellus combined the allozyme profiles of their diploid parents (T. dubius and T. porrifolius, and T. dubius and T. pratensis, respectively). This classic paper addressed the link between genotype and biochemical phenotype and documented enzyme additivity in allopolyploids. Perhaps more important than their model of additivity, however, was their demonstration of novelty at the biochemical level. Enzyme multiplicity-the production of novel enzyme forms in the allopolyploids-can provide an extensive array of polymorphism for a polyploid individual and may explain, for example, the expanded ranges of polyploids relative to their diploid progenitors. In this paper, we extend the concept of evolutionary novelty in allopolyploids to a range of genetic and ecological features. We observe that the dynamic nature of polyploid genomes-with alterations in gene content, gene number, gene arrangement, gene expression and transposon activity-may generate sufficient novelty that every individual in a polyploid population or species may be unique. Whereas certain combinations of these features will undoubtedly be maladaptive, some unique combinations of newly generated variation may provide tremendous evolutionary potential and adaptive capabilities.

Citing Articles

When Genetic Diversity Is Low: The Effects of Ploidy Level on Plant Functional Trait Expression in Under Global Change.

Granse D, Wendt P, Suchrow S, Hanelt D, Fromm J, Milin M Ecol Evol. 2025; 15(3):e71022.

PMID: 40027418 PMC: 11872210. DOI: 10.1002/ece3.71022.


Differential Gene Expression and Unbalanced Homeolog Expression Bias in 4 Million-Year-Old Allopolyploids of Nicotiana Section Repandae.

Ostovar T, Landis J, McCarthy E, Sierro N, Litt A Genome Biol Evol. 2025; 17(3).

PMID: 39973064 PMC: 11890095. DOI: 10.1093/gbe/evaf029.


Natural neopolyploids: a stimulus for novel research.

Edger P, Soltis D, Yoshioka S, Vallejo-Marin M, Shimizu-Inatsugi R, Shimizu K New Phytol. 2025; 246(1):78-93.

PMID: 39953679 PMC: 11883059. DOI: 10.1111/nph.20437.


Every Gain Comes With Loss: Ecological and Physiological Shifts Associated With Polyploidization in a Pygmy Frog.

Chen Q, Zhu W, Chang L, Zhang M, Wang S, Liu J Mol Biol Evol. 2025; 42(2).

PMID: 39918026 PMC: 11840752. DOI: 10.1093/molbev/msaf037.


Accurate Inference of the Polyploid Continuum Using Forward-Time Simulations.

Dunn T, Sethuraman A Mol Biol Evol. 2024; 41(12).

PMID: 39549274 PMC: 11669724. DOI: 10.1093/molbev/msae241.


References
1.
Hodgson J, Sharafi M, Jalili A, Diaz S, Montserrat-Marti G, Palmer C . Stomatal vs. genome size in angiosperms: the somatic tail wagging the genomic dog?. Ann Bot. 2010; 105(4):573-84. PMC: 2850795. DOI: 10.1093/aob/mcq011. View

2.
Tate J, Symonds V, Doust A, Buggs R, Mavrodiev E, Majure L . Synthetic polyploids of Tragopogon miscellus and T. mirus (Asteraceae): 60 Years after Ownbey's discovery. Am J Bot. 2011; 96(5):979-88. DOI: 10.3732/ajb.0800299. View

3.
Garsmeur O, Schnable J, Almeida A, Jourda C, DHont A, Freeling M . Two evolutionarily distinct classes of paleopolyploidy. Mol Biol Evol. 2013; 31(2):448-54. DOI: 10.1093/molbev/mst230. View

4.
Golding G, Strobeck C . INCREASED NUMBER OF ALLELES FOUND IN HYBRID POPULATIONS DUE TO INTRAGENIC RECOMBINATION. Evolution. 2017; 37(1):17-29. DOI: 10.1111/j.1558-5646.1983.tb05510.x. View

5.
Tate J, Joshi P, Soltis K, Soltis P, Soltis D . On the road to diploidization? Homoeolog loss in independently formed populations of the allopolyploid Tragopogon miscellus (Asteraceae). BMC Plant Biol. 2009; 9:80. PMC: 2708164. DOI: 10.1186/1471-2229-9-80. View