Development and selective grain make plasticity 'take the lead' in adaptive evolution
Development and selective grain make plasticity 'take the lead' in adaptive evolution
Background
Biological evolution exhibits an extraordinary capability to adapt organisms to their environments. The explanation for this often takes for granted that random genetic variation produces at least some beneficial phenotypic variation in which natural selection can act. Such genetic evolvability could itself be a product of evolution, but it is widely acknowledged that the immediate selective gains of evolvability are small on short timescales. So how do biological systems come to exhibit such extraordinary capacity to evolve? One suggestion is that adaptive phenotypic plasticity makes genetic evolution find adaptations faster. However, the need to explain the origin of adaptive plasticity puts genetic evolution back in the driving seat, and genetic evolvability remains unexplained.
Results
To better understand the interaction between plasticity and genetic evolvability, we simulate the evolution of phenotypes produced by gene-regulation network-based models of development. First, we show that the phenotypic variation resulting from genetic and environmental perturbation are highly concordant. This is because phenotypic variation, regardless of its cause, occurs within the relatively specific space of possibilities allowed by development. Second, we show that selection for genetic evolvability results in the evolution of adaptive plasticity and vice versa. This linkage is essentially symmetric but, unlike genetic evolvability, the selective gains of plasticity are often substantial on short, including within-lifetime, timescales. Accordingly, we show that selection for phenotypic plasticity can be effective in promoting the evolution of high genetic evolvability.
Conclusions
Without overlooking the fact that adaptive plasticity is itself a product of genetic evolution, we show how past selection for plasticity can exercise a disproportionate effect on genetic evolvability and, in turn, influence the course of adaptive evolution.
Brun-Usan, Miguel A
5d7fffc6-3cae-4c6d-92a5-0897a737b410
Rago, Alfredo
12ff6af9-c7dc-4eb2-9bdf-43c876c19737
Uller, Tobias
05ac1f63-5fd6-490d-8f9f-f7d3ed62b948
Watson, Richard
ce199dfc-d5d4-4edf-bd7b-f9e224c96c75
20 November 2021
Brun-Usan, Miguel A
5d7fffc6-3cae-4c6d-92a5-0897a737b410
Rago, Alfredo
12ff6af9-c7dc-4eb2-9bdf-43c876c19737
Uller, Tobias
05ac1f63-5fd6-490d-8f9f-f7d3ed62b948
Watson, Richard
ce199dfc-d5d4-4edf-bd7b-f9e224c96c75
Brun-Usan, Miguel A, Rago, Alfredo, Thies, Christoph, Uller, Tobias and Watson, Richard
(2021)
Development and selective grain make plasticity 'take the lead' in adaptive evolution.
BMC Ecology and Evolution, 21, [205].
(doi:10.1186/s12862-021-01936-0).
Abstract
Background
Biological evolution exhibits an extraordinary capability to adapt organisms to their environments. The explanation for this often takes for granted that random genetic variation produces at least some beneficial phenotypic variation in which natural selection can act. Such genetic evolvability could itself be a product of evolution, but it is widely acknowledged that the immediate selective gains of evolvability are small on short timescales. So how do biological systems come to exhibit such extraordinary capacity to evolve? One suggestion is that adaptive phenotypic plasticity makes genetic evolution find adaptations faster. However, the need to explain the origin of adaptive plasticity puts genetic evolution back in the driving seat, and genetic evolvability remains unexplained.
Results
To better understand the interaction between plasticity and genetic evolvability, we simulate the evolution of phenotypes produced by gene-regulation network-based models of development. First, we show that the phenotypic variation resulting from genetic and environmental perturbation are highly concordant. This is because phenotypic variation, regardless of its cause, occurs within the relatively specific space of possibilities allowed by development. Second, we show that selection for genetic evolvability results in the evolution of adaptive plasticity and vice versa. This linkage is essentially symmetric but, unlike genetic evolvability, the selective gains of plasticity are often substantial on short, including within-lifetime, timescales. Accordingly, we show that selection for phenotypic plasticity can be effective in promoting the evolution of high genetic evolvability.
Conclusions
Without overlooking the fact that adaptive plasticity is itself a product of genetic evolution, we show how past selection for plasticity can exercise a disproportionate effect on genetic evolvability and, in turn, influence the course of adaptive evolution.
Text
s12862-021-01936-0
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More information
Accepted/In Press date: 10 November 2021
Published date: 20 November 2021
Identifiers
Local EPrints ID: 471171
URI: http://eprints.soton.ac.uk/id/eprint/471171
ISSN: 2730-7182
PURE UUID: 2acc2f5a-d353-49b5-b27c-7d7323fa9fdd
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Date deposited: 28 Oct 2022 17:52
Last modified: 17 Mar 2024 03:00
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Contributors
Author:
Miguel A Brun-Usan
Author:
Alfredo Rago
Author:
Christoph Thies
Author:
Tobias Uller
Author:
Richard Watson
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