DIFFERENTIAL INTROGRESSION IN A MOSAIC HYBRID ZONE REVEALS CANDIDATE BARRIER GENES

Hybrid zones act as genomic sieves. Although globally advantageous alleles will spread throughout the zone and neutral alleles can be freely exchanged between species, introgression will be restricted for genes that contribute to reproductive barriers or local adaptation. Seminal fluid proteins (SFP...

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Published inEvolution Vol. 67; no. 12; pp. 3653 - 3661
Main Authors Larson, Erica L., Andrés, Jose A., Bogdanowicz, Steven M., Harrison, Richard G.
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.12.2013
Wiley Subscription Services, Inc
Oxford University Press
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ISSN0014-3820
1558-5646
1558-5646
DOI10.1111/evo.12205

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Summary:Hybrid zones act as genomic sieves. Although globally advantageous alleles will spread throughout the zone and neutral alleles can be freely exchanged between species, introgression will be restricted for genes that contribute to reproductive barriers or local adaptation. Seminal fluid proteins (SFPs) are known to contribute to reproductive barriers in insects and have been proposed as candidate barrier genes in the hybridizing field crickets Gryllus pennsylvanicus and Gryllus firmus. Here, we have used 125 single nucleotide polymorphisms to characterize patterns of differential introgression and to identify genes that may contribute to prezygotic barriers between these species. Using a transcriptome scan of the male cricket accessory gland (the site of SFP synthesis), we identified genes with major allele frequency differences between the species. We then compared patterns of introgression for genes encoding SFPs with patterns for genes expressed in the same tissue that do not encode SFPs. We find no evidence that SFPs have reduced gene exchange across the cricket hybrid zone. However, a number of genes exhibit dramatically reduced introgression, and many of these genes encode proteins with functional roles consistent with known barriers.
Bibliography:istex:B9E57BFA93B2458F652E5C39E7E76678691A1950
National Science Foundation - No. DEB-0639904
ark:/67375/WNG-GB35W7T1-5
ArticleID:EVO12205
Figure S1. Individual genomic clines for all 125 markers analyzed.Table S1. Sampled allopatric and mixed populations of Gryllus pennsylvanicus and Gryllus firmus used for single nucleotide polymorphism validation. Table S2. Sampling locations and number of crickets collected per locality (N) for the southern Pennsylvania region of the hybrid zone. Table S3. Amplification and genotyping success of 232 single nucleotide polymorphism markers (181 genes) for a panel of 71 crickets from six allopatric populations (Gryllus pennsylvanicus = 35, Gryllus firmus =36) and nine crickets from a single mixed population. Table S4. Allele frequencies in allopatric populations of Gryllus pennsylvanicus and Gryllus firmus for 154 single nucleotide polymorphism markers successfully genotyped. Table S5. Sequence descriptions and functional annotation from Andres et al. (2013) for 125 single nucleotide polymorphisms used in genomic cline analysis. Table S6. Results of genomic cline analysis for 125 markers genotyped in the Pennsylvania portion of the hybrid zone between Gryllus firmus and Gryllus pennsylvanicus. Table S7. Genotyping results of a representative single nucleotide polymorphism for each of the 15 genes encoding seminal fluid proteins assayed.
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ISSN:0014-3820
1558-5646
1558-5646
DOI:10.1111/evo.12205