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No evidence for maintenance of a sympatric Heliconius species barrier by chromosomal inversions
Mechanisms that suppress recombination are known to help maintain species barriers by preventing the breakup of coadapted gene combinations. The sympatric butterfly species Heliconius melpomene and Heliconius cydno are separated by many strong barriers, but the species still hybridize infrequently i...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122123/ https://www.ncbi.nlm.nih.gov/pubmed/30283645 http://dx.doi.org/10.1002/evl3.12 |
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author | Davey, John W. Barker, Sarah L. Rastas, Pasi M. Pinharanda, Ana Martin, Simon H. Durbin, Richard McMillan, W. Owen Merrill, Richard M. Jiggins, Chris D. |
author_facet | Davey, John W. Barker, Sarah L. Rastas, Pasi M. Pinharanda, Ana Martin, Simon H. Durbin, Richard McMillan, W. Owen Merrill, Richard M. Jiggins, Chris D. |
author_sort | Davey, John W. |
collection | PubMed |
description | Mechanisms that suppress recombination are known to help maintain species barriers by preventing the breakup of coadapted gene combinations. The sympatric butterfly species Heliconius melpomene and Heliconius cydno 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 H. melpomene and H. cydno. |
format | Online Article Text |
id | pubmed-6122123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61221232018-10-03 No evidence for maintenance of a sympatric Heliconius species barrier by chromosomal inversions Davey, John W. Barker, Sarah L. Rastas, Pasi M. Pinharanda, Ana Martin, Simon H. Durbin, Richard McMillan, W. Owen Merrill, Richard M. Jiggins, Chris D. Evol Lett Letters Mechanisms that suppress recombination are known to help maintain species barriers by preventing the breakup of coadapted gene combinations. The sympatric butterfly species Heliconius melpomene and Heliconius cydno 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 H. melpomene and H. cydno. John Wiley and Sons Inc. 2017-06-14 /pmc/articles/PMC6122123/ /pubmed/30283645 http://dx.doi.org/10.1002/evl3.12 Text en © 2017 The Author(s). Evolution Letters published by Wiley Periodicals, Inc. on behalf of Society for the Study of Evolution (SSE) and European Society for Evolutionary Biology (ESEB). This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Letters Davey, John W. Barker, Sarah L. Rastas, Pasi M. Pinharanda, Ana Martin, Simon H. Durbin, Richard McMillan, W. Owen Merrill, Richard M. Jiggins, Chris D. No evidence for maintenance of a sympatric Heliconius species barrier by chromosomal inversions |
title | No evidence for maintenance of a sympatric Heliconius species barrier by chromosomal inversions |
title_full | No evidence for maintenance of a sympatric Heliconius species barrier by chromosomal inversions |
title_fullStr | No evidence for maintenance of a sympatric Heliconius species barrier by chromosomal inversions |
title_full_unstemmed | No evidence for maintenance of a sympatric Heliconius species barrier by chromosomal inversions |
title_short | No evidence for maintenance of a sympatric Heliconius species barrier by chromosomal inversions |
title_sort | no evidence for maintenance of a sympatric heliconius species barrier by chromosomal inversions |
topic | Letters |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122123/ https://www.ncbi.nlm.nih.gov/pubmed/30283645 http://dx.doi.org/10.1002/evl3.12 |
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