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      Genetic, morphometric, and molecular analyses of interspecies differences in head shape and hybrid developmental defects in the wasp genus Nasonia

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          Abstract

          Males in the parasitoid wasp genus Nasonia have distinct, species-specific, head shapes. The availability of fertile hybrids among the species, along with obligate haploidy of males, facilitates analysis of complex gene interactions in development and evolution. Previous analyses showed that both the divergence in head shape between Nasonia vitripennis and Nasonia giraulti, and the head-specific developmental defects of F2 haploid hybrid males, are governed by multiple changes in networks of interacting genes. Here, we extend our understanding of the gene interactions that affect morphogenesis in male heads. Use of artificial diploid male hybrids shows that alleles mediating developmental defects are recessive, while there are diverse dominance relationships among other head shape traits. At the molecular level, the sex determination locus doublesex plays a major role in male head shape differences, but it is not the only important factor. Introgression of a giraulti region on chromsome 2 reveals a recessive locus that causes completely penetrant head clefting in both males and females in a vitripennis background. Finally, a third species ( N. longicornis) was used to investigate the timing of genetic changes related to head morphology, revealing that most changes causing defects arose after the divergence of N. vitripennis from the other species, but prior to the divergence of N. giraulti and N. longicornis from each other. Our results demonstrate that developmental gene networks can be dissected using interspecies crosses in Nasonia, and set the stage for future fine-scale genetic dissection of both head shape and hybrid developmental defects.

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          Most cited references57

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          Epistasis--the essential role of gene interactions in the structure and evolution of genetic systems.

          Epistasis, or interactions between genes, has long been recognized as fundamentally important to understanding the structure and function of genetic pathways and the evolutionary dynamics of complex genetic systems. With the advent of high-throughput functional genomics and the emergence of systems approaches to biology, as well as a new-found ability to pursue the genetic basis of evolution down to specific molecular changes, there is a renewed appreciation both for the importance of studying gene interactions and for addressing these questions in a unified, quantitative manner.
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            Extensions of the Procrustes Method for the Optimal Superimposition of Landmarks

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              Epistasis and quantitative traits: using model organisms to study gene-gene interactions.

              The role of epistasis in the genetic architecture of quantitative traits is controversial, despite the biological plausibility that nonlinear molecular interactions underpin the genotype-phenotype map. This controversy arises because most genetic variation for quantitative traits is additive. However, additive variance is consistent with pervasive epistasis. In this Review, I discuss experimental designs to detect the contribution of epistasis to quantitative trait phenotypes in model organisms. These studies indicate that epistasis is common, and that additivity can be an emergent property of underlying genetic interaction networks. Epistasis causes hidden quantitative genetic variation in natural populations and could be responsible for the small additive effects, missing heritability and the lack of replication that are typically observed for human complex traits.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                G3 (Bethesda)
                Genetics
                g3journal
                G3: Genes|Genomes|Genetics
                Oxford University Press
                2160-1836
                December 2021
                02 September 2021
                02 September 2021
                : 11
                : 12
                : jkab313
                Affiliations
                [1 ] Biological Sciences, University of Illinois at Chicago , Chicago, IL 60607, USA
                [2 ] Optical Imaging Core, Van Andel Institute , Grand Rapids, MI 49503, USA
                [3 ] Department of Biology, University of Rochester , Rochester, NY 14627, USA
                [4 ] Department of Ecology and Evolution, University of Chicago , Chicago, IL 60637, USA
                Author notes
                Corresponding author: 900 South Ashland Ave., Rm 4018, Chicago, IL 60607, USA. Email: jlynch42@ 123456uic.edu
                Author information
                https://orcid.org/0000-0001-8950-9572
                https://orcid.org/0000-0001-7625-657X
                Article
                jkab313
                10.1093/g3journal/jkab313
                8664464
                34580730
                3377dc11-5c4b-45d1-90bb-98d478701544
                © The Author(s) 2021. Published by Oxford University Press on behalf of Genetics Society of America.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 06 June 2019
                : 26 August 2021
                : 04 December 2021
                Page count
                Pages: 12
                Funding
                Funded by: National Institutes of Health, DOI 10.13039/100000002;
                Award ID: R01GM129153
                Award ID: R03HD087476
                Funded by: National Institutes of Health, DOI 10.13039/100000002;
                Award ID: GM70026
                Funded by: National Sciene Foundation;
                Award ID: IOS-1456233
                Funded by: NSF, DOI 10.13039/100000001;
                Award ID: 1950078
                Funded by: Nathaniel and Helen Wisch Chair in Biology;
                Categories
                Investigation
                AcademicSubjects/SCI01180
                AcademicSubjects/SCI01140
                AcademicSubjects/SCI00010
                AcademicSubjects/SCI00960

                Genetics
                epistasis,complex traits,nasonia,hybrid compatibility,morphological development
                Genetics
                epistasis, complex traits, nasonia, hybrid compatibility, morphological development

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