Phenotypic stasis with genetic divergence

Whether or not genetic divergence in the short-term of tens to hundreds of generations is compatible with phenotypic stasis remains a relatively unexplored problem. We evolved predominantly outcrossing, genetically diverse populations of the nematode Caenorhabditis elegans under a constant and homog...

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Main Authors: Mallard, François, Noble, Luke, Guzella, Thiago, Afonso, Bruno, Baer, Charles F., Teotónio, Henrique
Format: Article
Language:English
Published: Peer Community In 2023-12-01
Series:Peer Community Journal
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Online Access:https://peercommunityjournal.org/articles/10.24072/pcjournal.349/
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author Mallard, François
Noble, Luke
Guzella, Thiago
Afonso, Bruno
Baer, Charles F.
Teotónio, Henrique
author_facet Mallard, François
Noble, Luke
Guzella, Thiago
Afonso, Bruno
Baer, Charles F.
Teotónio, Henrique
author_sort Mallard, François
collection DOAJ
description Whether or not genetic divergence in the short-term of tens to hundreds of generations is compatible with phenotypic stasis remains a relatively unexplored problem. We evolved predominantly outcrossing, genetically diverse populations of the nematode Caenorhabditis elegans under a constant and homogeneous environment for 240 generations and followed individual locomotion behavior. Although founders of lab populations show highly diverse locomotion behavior, during lab evolution, the component traits of locomotion behavior – defined as the transition rates in activity and direction – did not show divergence from the ancestral population. In contrast, transition rates’ genetic (co)variance structure showed a marked divergence from the ancestral state and differentiation among replicate populations during the final 100 generations and after most adaptation had been achieved. We observe that genetic differentiation is a transient pattern during the loss of genetic variance along phenotypic dimensions under drift during the last 100 generations of lab evolution. These results suggest that short-term stasis of locomotion behavior is maintained because of stabilizing selection, while the genetic structuring of component traits is contingent upon drift history.
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spelling doaj-art-360de8cea71a4fe590c325e16aedf19f2025-02-07T10:16:48ZengPeer Community InPeer Community Journal2804-38712023-12-01310.24072/pcjournal.34910.24072/pcjournal.349Phenotypic stasis with genetic divergence Mallard, François0https://orcid.org/0000-0003-2087-1914Noble, Luke1https://orcid.org/0000-0002-5161-4059Guzella, Thiago2Afonso, Bruno3Baer, Charles F.4https://orcid.org/0000-0002-0140-5814Teotónio, Henrique5https://orcid.org/0000-0003-1057-6882Institut de Biologie de l’École Normale Supérieure, CNRS UMR 8197, Inserm U1024, PSL Research University, F-75005 Paris, FranceInstitut de Biologie de l’École Normale Supérieure, CNRS UMR 8197, Inserm U1024, PSL Research University, F-75005 Paris, FranceInstitut de Biologie de l’École Normale Supérieure, CNRS UMR 8197, Inserm U1024, PSL Research University, F-75005 Paris, FranceInstitut de Biologie de l’École Normale Supérieure, CNRS UMR 8197, Inserm U1024, PSL Research University, F-75005 Paris, FranceDepartment of Biology, University of Florida Genetics Institute, University of Florida, Gainsville, Florida 32611, U.S.A.Institut de Biologie de l’École Normale Supérieure, CNRS UMR 8197, Inserm U1024, PSL Research University, F-75005 Paris, FranceWhether or not genetic divergence in the short-term of tens to hundreds of generations is compatible with phenotypic stasis remains a relatively unexplored problem. We evolved predominantly outcrossing, genetically diverse populations of the nematode Caenorhabditis elegans under a constant and homogeneous environment for 240 generations and followed individual locomotion behavior. Although founders of lab populations show highly diverse locomotion behavior, during lab evolution, the component traits of locomotion behavior – defined as the transition rates in activity and direction – did not show divergence from the ancestral population. In contrast, transition rates’ genetic (co)variance structure showed a marked divergence from the ancestral state and differentiation among replicate populations during the final 100 generations and after most adaptation had been achieved. We observe that genetic differentiation is a transient pattern during the loss of genetic variance along phenotypic dimensions under drift during the last 100 generations of lab evolution. These results suggest that short-term stasis of locomotion behavior is maintained because of stabilizing selection, while the genetic structuring of component traits is contingent upon drift history. https://peercommunityjournal.org/articles/10.24072/pcjournal.349/phenotypic stasisG-matrixselection surfacegenetic driftlocomotion behaviortransition ratesCaenorhabditis elegansexperimental evolutionphenotypic stasisG-matrixselection surfacegenetic driftlocomotion behaviortransition ratesCaenorhabditis elegansexperimental evolutionphenotypic stasisG-matrixselection surfacegenetic driftlocomotion behaviortransition ratesCaenorhabditis elegansexperimental evolution
spellingShingle Mallard, François
Noble, Luke
Guzella, Thiago
Afonso, Bruno
Baer, Charles F.
Teotónio, Henrique
Phenotypic stasis with genetic divergence
Peer Community Journal
phenotypic stasis
G-matrix
selection surface
genetic drift
locomotion behavior
transition rates
Caenorhabditis elegans
experimental evolution
phenotypic stasis
G-matrix
selection surface
genetic drift
locomotion behavior
transition rates
Caenorhabditis elegans
experimental evolution
phenotypic stasis
G-matrix
selection surface
genetic drift
locomotion behavior
transition rates
Caenorhabditis elegans
experimental evolution
title Phenotypic stasis with genetic divergence
title_full Phenotypic stasis with genetic divergence
title_fullStr Phenotypic stasis with genetic divergence
title_full_unstemmed Phenotypic stasis with genetic divergence
title_short Phenotypic stasis with genetic divergence
title_sort phenotypic stasis with genetic divergence
topic phenotypic stasis
G-matrix
selection surface
genetic drift
locomotion behavior
transition rates
Caenorhabditis elegans
experimental evolution
phenotypic stasis
G-matrix
selection surface
genetic drift
locomotion behavior
transition rates
Caenorhabditis elegans
experimental evolution
phenotypic stasis
G-matrix
selection surface
genetic drift
locomotion behavior
transition rates
Caenorhabditis elegans
experimental evolution
url https://peercommunityjournal.org/articles/10.24072/pcjournal.349/
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AT guzellathiago phenotypicstasiswithgeneticdivergence
AT afonsobruno phenotypicstasiswithgeneticdivergence
AT baercharlesf phenotypicstasiswithgeneticdivergence
AT teotoniohenrique phenotypicstasiswithgeneticdivergence