Steep clines within a highly permeable genome across a hybrid zone between two subspecies of the European rabbit

Maintenance of genetic distinction in the face of gene flow is an important aspect of the speciation process. Here, we provide a detailed spatial and genetic characterization of a hybrid zone between two subspecies of the European rabbit. We examined patterns of allele frequency change for 22 marker...

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Published inMolecular ecology Vol. 22; no. 9; pp. 2511 - 2525
Main Authors Carneiro, Miguel, Baird, Stuart J. E, Afonso, Sandra, Ramirez, Esther, Tarroso, Pedro, Teotónio, Henrique, Villafuerte, Rafael, Nachman, Michael W, Ferrand, Nuno
Format Journal Article
LanguageEnglish
Published Oxford Blackwell Publishing Ltd 01.05.2013
Blackwell
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Summary:Maintenance of genetic distinction in the face of gene flow is an important aspect of the speciation process. Here, we provide a detailed spatial and genetic characterization of a hybrid zone between two subspecies of the European rabbit. We examined patterns of allele frequency change for 22 markers located on the autosomes, X‐chromosome, Y‐chromosome and mtDNA in 1078 individuals sampled across the hybrid zone. While some loci revealed extremely wide clines (w ≥ 300 km) relative to an estimated dispersal of 1.95–4.22 km/generation, others showed abrupt transitions (w ≈ 10 km), indicating localized genomic regions of strong selection against introgression. The subset of loci showing steep clines had largely coincident centers and stepped changes in allele frequency that did not co‐localize with any physical barrier or ecotone, suggesting that the rabbit hybrid zone is a tension zone. The steepest clines were for X‐ and Y‐chromosome markers. Our results are consistent with previous inference based on DNA sequence variation of individuals sampled in allopatry in suggesting that a large proportion of each genome has escaped the overall barrier to gene flow in the middle of the hybrid zone. These results imply an old history of hybridization and high effective gene flow and anticipate that isolation factors should often localize to small genomic regions.
Bibliography:http://dx.doi.org/10.1111/mec.12272
ArticleID:MEC12272
National Science Foundation and National Institutes of Health
European Social Fund and Portuguese MCTES - No. SFRH/BD/23786/2005; No. SFRH/BPD/72343/2010
Fundação para a Ciência e a Tecnologia - No. PTDC/BIA-BDE/72304/2006; No. PTDC/BIA-EVF/111368/2009; No. PTDC/CVT/122943/2010; No. CGL2009-11665; No. POII09-0099-2557
Fundação para a Ciência e a Tecnologia - No. PTDC/BIA-BEC/103440/2008
istex:34537B8DF138C84863CFB08005ACF49720042076
Table S1 Locality details and numbers of individuals sampled. Table S2 PCR and extension primers used in the Sequenom's iPlex genotyping. Table S3 Maximum likelihood estimates (MLE) for the two parameters of the non-geographic concordance analysis (α and β) and probability of non-concordant introgression patterns for each locus. Fig. S1 Likelihood profiles for monotonic change in allele frequencies across the sampling area. Fig. S2 A summary of clinal patterns for all individual loci without constraint to any particular model of monotonic change. Fig. S3 Likelihood profiles for cline center (c) and cline width (w) estimated under the cline model retained for each locus. Fig. S4 Consensus Hardy-Weinberg (FIS) values across the center of the rabbit hybrid zone (indicated by a solid vertical line). Fig. S5 Scatterplot of cline width (km) versus net nucleotide divergence (Da; A) and locus specific estimates of gene flow between Oryctolagus algirus and O. c. cuniculus individuals sampled away from the hybrid zone (data from Carneiro et al. , ). Fig. S6 Map of the study area with major topographic features.
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ISSN:0962-1083
1365-294X
DOI:10.1111/mec.12272