Fluctuating environments select for short-term phenotypic variation leading to long-term exploration.

Genetic spaces are often described in terms of fitness landscapes or genotype-to-phenotype maps, where each genetic sequence is associated with phenotypic properties and linked to other genotypes that are a single mutational step away. The positions close to a genotype make up its "mutational l...

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Main Authors: Rosangela Canino-Koning, Michael J Wiser, Charles Ofria
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-04-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC6474582?pdf=render
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spelling doaj-0ac57eb8fb444b4492ba83629785107c2020-11-25T01:57:43ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582019-04-01154e100644510.1371/journal.pcbi.1006445Fluctuating environments select for short-term phenotypic variation leading to long-term exploration.Rosangela Canino-KoningMichael J WiserCharles OfriaGenetic spaces are often described in terms of fitness landscapes or genotype-to-phenotype maps, where each genetic sequence is associated with phenotypic properties and linked to other genotypes that are a single mutational step away. The positions close to a genotype make up its "mutational landscape" and, in aggregate, determine the short-term evolutionary potential of a population. Populations with wider ranges of phenotypes in their mutational neighborhood are known to be more evolvable. Likewise, those with fewer phenotypic changes available in their local neighborhoods are more mutationally robust. Here, we examine whether forces that change the distribution of phenotypes available by mutation profoundly alter subsequent evolutionary dynamics. We compare evolved populations of digital organisms that were subject to either static or cyclically-changing environments. For each of these, we examine diversity of the phenotypes that are produced through mutations in order to characterize the local genotype-phenotype map. We demonstrate that environmental change can push populations toward more evolvable mutational landscapes where many alternate phenotypes are available, though purely deleterious mutations remain suppressed. Further, we show that populations in environments with harsh changes switch phenotypes more readily than those in environments with more benign changes. We trace this effect to repeated population bottlenecks in the harsh environments, which result in shorter coalescence times and keep populations in regions of the mutational landscape where the phenotypic shifts in question are more likely to occur. Typically, static environments select solely for immediate optimization, at the expensive of long-term evolvability. In contrast, we show that with changing environments, short-term pressures to deal with immediate challenges can align with long-term pressures to explore a more productive portion of the mutational landscape.http://europepmc.org/articles/PMC6474582?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Rosangela Canino-Koning
Michael J Wiser
Charles Ofria
spellingShingle Rosangela Canino-Koning
Michael J Wiser
Charles Ofria
Fluctuating environments select for short-term phenotypic variation leading to long-term exploration.
PLoS Computational Biology
author_facet Rosangela Canino-Koning
Michael J Wiser
Charles Ofria
author_sort Rosangela Canino-Koning
title Fluctuating environments select for short-term phenotypic variation leading to long-term exploration.
title_short Fluctuating environments select for short-term phenotypic variation leading to long-term exploration.
title_full Fluctuating environments select for short-term phenotypic variation leading to long-term exploration.
title_fullStr Fluctuating environments select for short-term phenotypic variation leading to long-term exploration.
title_full_unstemmed Fluctuating environments select for short-term phenotypic variation leading to long-term exploration.
title_sort fluctuating environments select for short-term phenotypic variation leading to long-term exploration.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2019-04-01
description Genetic spaces are often described in terms of fitness landscapes or genotype-to-phenotype maps, where each genetic sequence is associated with phenotypic properties and linked to other genotypes that are a single mutational step away. The positions close to a genotype make up its "mutational landscape" and, in aggregate, determine the short-term evolutionary potential of a population. Populations with wider ranges of phenotypes in their mutational neighborhood are known to be more evolvable. Likewise, those with fewer phenotypic changes available in their local neighborhoods are more mutationally robust. Here, we examine whether forces that change the distribution of phenotypes available by mutation profoundly alter subsequent evolutionary dynamics. We compare evolved populations of digital organisms that were subject to either static or cyclically-changing environments. For each of these, we examine diversity of the phenotypes that are produced through mutations in order to characterize the local genotype-phenotype map. We demonstrate that environmental change can push populations toward more evolvable mutational landscapes where many alternate phenotypes are available, though purely deleterious mutations remain suppressed. Further, we show that populations in environments with harsh changes switch phenotypes more readily than those in environments with more benign changes. We trace this effect to repeated population bottlenecks in the harsh environments, which result in shorter coalescence times and keep populations in regions of the mutational landscape where the phenotypic shifts in question are more likely to occur. Typically, static environments select solely for immediate optimization, at the expensive of long-term evolvability. In contrast, we show that with changing environments, short-term pressures to deal with immediate challenges can align with long-term pressures to explore a more productive portion of the mutational landscape.
url http://europepmc.org/articles/PMC6474582?pdf=render
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