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No Evidence for Maintenance of a Sympatric Species Barrier by Chromosomal Inversions

Overview
Journal Evol Lett
Specialty Biology
Date 2018 Oct 5
PMID 30283645
Citations 41
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Abstract

Mechanisms that suppress recombination are known to help maintain species barriers by preventing the breakup of coadapted gene combinations. The sympatric butterfly species and are separated by many strong barriers, but the species still hybridize infrequently in the wild, and around 40% of the genome is influenced by introgression. We tested the hypothesis that genetic barriers between the species are maintained by inversions or other mechanisms that reduce between-species recombination rate. We constructed fine-scale recombination maps for Panamanian populations of both species and their hybrids to directly measure recombination rate within and between species, and generated long sequence reads to detect inversions. We find no evidence for a systematic reduction in recombination rates in F1 hybrids, and also no evidence for inversions longer than 50 kb that might be involved in generating or maintaining species barriers. This suggests that mechanisms leading to global or local reduction in recombination do not play a significant role in the maintenance of species barriers between and .

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References
1.
Martin S, Most M, Palmer W, Salazar C, McMillan W, Jiggins F . Natural Selection and Genetic Diversity in the Butterfly Heliconius melpomene. Genetics. 2016; 203(1):525-41. PMC: 4858797. DOI: 10.1534/genetics.115.183285. View

2.
Nadeau N, Ruiz M, Salazar P, Counterman B, Medina J, Ortiz-Zuazaga H . Population genomics of parallel hybrid zones in the mimetic butterflies, H. melpomene and H. erato. Genome Res. 2014; 24(8):1316-33. PMC: 4120085. DOI: 10.1101/gr.169292.113. View

3.
Joron M, Frezal L, Jones R, Chamberlain N, Lee S, Haag C . Chromosomal rearrangements maintain a polymorphic supergene controlling butterfly mimicry. Nature. 2011; 477(7363):203-6. PMC: 3717454. DOI: 10.1038/nature10341. View

4.
Naisbit R, Jiggins C, Mallet J . Disruptive sexual selection against hybrids contributes to speciation between Heliconius cydno and Heliconius melpomene. Proc Biol Sci. 2001; 268(1478):1849-54. PMC: 1088818. DOI: 10.1098/rspb.2001.1753. View

5.
Arias C, Salazar C, Rosales C, Kronforst M, Linares M, Bermingham E . Phylogeography of Heliconius cydno and its closest relatives: disentangling their origin and diversification. Mol Ecol. 2014; 23(16):4137-52. DOI: 10.1111/mec.12844. View