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Published on: August 12, 2019
Widespread cryptic variation in genetic architecture between the sexes
Wouter van der Bijl1,2, Judith E Mank1,2,3
1Department of Zoology University of British Columbia Vancouver BC V6T 1Z4 Canada.
Sexual dimorphism (SD) arises from sex-specific genetic architecture, not just differential gene regulation. Gene knockouts reveal hidden genetic differences between sexes influencing traits, offering new insights into evolutionary biology.
Area of Science:
- Evolutionary Biology
- Genetics
- Developmental Biology
Background:
- Most of the genome is shared between sexes, suggesting shared genetic architecture for most traits.
- Shared genetic architecture is often considered a constraint on the evolution of sexual dimorphism (SD).
- SD is prevalent, leading to the hypothesis that it arises from differential regulation of shared genetic architecture.
Purpose of the Study:
- To investigate how regulatory variation influences sexual dimorphism (SD).
- To explore the effects of gene knockout mutations on mouse phenotypes and their sex-specific impacts.
- To understand the genetic basis of SD and its relationship with sex-specific genetic architecture.
Main Methods:
- Studied the phenotypic effects of thousands of gene knockout mutations in mice.
- Analyzed 202 different mouse phenotypes to assess sexual dimorphism.
- Examined sex-specific phenotypic effects of gene knockouts and regulatory changes.
Main Results:
- Many mouse traits exhibit some degree of sexual dimorphism.
- A significant proportion of gene knockouts display sex-specific phenotypic effects.
- Cryptic differences in genetic architecture between sexes were identified for many traits, leading to sexually discordant effects from concordant regulatory changes.
Conclusions:
- Sexual dimorphism can arise through sex-specific genetic architecture, independent of differential regulation of shared architecture.
- Regulatory variation plays a crucial role in generating sex-specific phenotypic effects.
- This study provides an alternative mechanism for the evolution of sexual dimorphism.
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