Literature DB >> 34864966

The relative impact of evolving pleiotropy and mutational correlation on trait divergence.

Jobran Chebib1,2, Frédéric Guillaume1,3.   

Abstract

Both pleiotropic connectivity and mutational correlations can restrict the decoupling of traits under divergent selection, but it is unknown which is more important in trait evolution. To address this question, we create a model that permits within-population variation in both pleiotropic connectivity and mutational correlation, and compare their relative importance to trait evolution. Specifically, we developed an individual-based stochastic model where mutations can affect whether a locus affects a trait and the extent of mutational correlations in a population. We find that traits can decouple whether there is evolution in pleiotropic connectivity or mutational correlation, but when both can evolve, then evolution in pleiotropic connectivity is more likely to allow for decoupling to occur. The most common genotype found in this case is characterized by having one locus that maintains connectivity to all traits and another that loses connectivity to the traits under stabilizing selection (subfunctionalization). This genotype is favored because it allows the subfunctionalized locus to accumulate greater effect size alleles, contributing to increasingly divergent trait values in the traits under divergent selection without changing the trait values of the other traits (genetic modularization). These results provide evidence that partial subfunctionalization of pleiotropic loci may be a common mechanism of trait decoupling under regimes of corridor selection.
© The Author(s) 2021. Published by Oxford University Press on behalf of Genetics Society of America. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  correlated mutation; correlational selection; genetic architecture; genetic constraints; metamerism; modularity; mutation; pleiotropy; subfunctionalization; trait divergence

Mesh:

Year:  2022        PMID: 34864966      PMCID: PMC8733425          DOI: 10.1093/genetics/iyab205

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  1 in total

1.  AMBRA1 p.Gln30Arg Mutation, Identified in a Cowden Syndrome Family, Exhibits Hyperproliferative Potential in hTERT-RPE1 Cells.

Authors:  Sundaramoorthy Revathidevi; Kazuyoshi Hosomichi; Toyoaki Natsume; Hirofumi Nakaoka; Naoko T Fujito; Hisako Akatsuka; Takehito Sato; Arasambattu Kannan Munirajan; Ituro Inoue
Journal:  Int J Mol Sci       Date:  2022-09-22       Impact factor: 6.208

  1 in total

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