Selection against accumulating mutations in niche-preference genes can drive speciation.

Our current understanding of sympatric speciation is that it occurs primarily through disruptive selection on ecological genes driven by competition, followed by reproductive isolation through reinforcement-like selection against inferior intermediates/heterozygotes. Our evolutionary model of select...

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Main Authors: Niclas Norrström, Wayne M Getz, Noél M A Holmgren
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3246506?pdf=render
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spelling doaj-8630580fc5904a2e9b703eca76e63e542020-11-25T02:08:04ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-01612e2948710.1371/journal.pone.0029487Selection against accumulating mutations in niche-preference genes can drive speciation.Niclas NorrströmWayne M GetzNoél M A HolmgrenOur current understanding of sympatric speciation is that it occurs primarily through disruptive selection on ecological genes driven by competition, followed by reproductive isolation through reinforcement-like selection against inferior intermediates/heterozygotes. Our evolutionary model of selection on resource recognition and preference traits suggests a new mechanism for sympatric speciation. We find speciation can occur in three phases. First a polymorphism of functionally different phenotypes is established through evolution of specialization. On the gene level, regulatory functions have evolved in which some alleles are conditionally switched off (i.e. are silent). These alleles accumulate harmful mutations that potentially may be expressed in offspring through recombination. Second mating associated with resource preference invades because harmful mutations in parents are not expressed in the offspring when mating assortatively, thereby dividing the population into two pre-zygotically isolated resource-specialist lineages. Third, silent alleles that evolved in phase one now accumulate deleterious mutations over the following generations in a Bateson-Dobzhansky-Muller fashion, establishing a post-zygotic barrier to hybridization.http://europepmc.org/articles/PMC3246506?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Niclas Norrström
Wayne M Getz
Noél M A Holmgren
spellingShingle Niclas Norrström
Wayne M Getz
Noél M A Holmgren
Selection against accumulating mutations in niche-preference genes can drive speciation.
PLoS ONE
author_facet Niclas Norrström
Wayne M Getz
Noél M A Holmgren
author_sort Niclas Norrström
title Selection against accumulating mutations in niche-preference genes can drive speciation.
title_short Selection against accumulating mutations in niche-preference genes can drive speciation.
title_full Selection against accumulating mutations in niche-preference genes can drive speciation.
title_fullStr Selection against accumulating mutations in niche-preference genes can drive speciation.
title_full_unstemmed Selection against accumulating mutations in niche-preference genes can drive speciation.
title_sort selection against accumulating mutations in niche-preference genes can drive speciation.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description Our current understanding of sympatric speciation is that it occurs primarily through disruptive selection on ecological genes driven by competition, followed by reproductive isolation through reinforcement-like selection against inferior intermediates/heterozygotes. Our evolutionary model of selection on resource recognition and preference traits suggests a new mechanism for sympatric speciation. We find speciation can occur in three phases. First a polymorphism of functionally different phenotypes is established through evolution of specialization. On the gene level, regulatory functions have evolved in which some alleles are conditionally switched off (i.e. are silent). These alleles accumulate harmful mutations that potentially may be expressed in offspring through recombination. Second mating associated with resource preference invades because harmful mutations in parents are not expressed in the offspring when mating assortatively, thereby dividing the population into two pre-zygotically isolated resource-specialist lineages. Third, silent alleles that evolved in phase one now accumulate deleterious mutations over the following generations in a Bateson-Dobzhansky-Muller fashion, establishing a post-zygotic barrier to hybridization.
url http://europepmc.org/articles/PMC3246506?pdf=render
work_keys_str_mv AT niclasnorrstrom selectionagainstaccumulatingmutationsinnichepreferencegenescandrivespeciation
AT waynemgetz selectionagainstaccumulatingmutationsinnichepreferencegenescandrivespeciation
AT noelmaholmgren selectionagainstaccumulatingmutationsinnichepreferencegenescandrivespeciation
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