Reproductive Isolation through Experimental Manipulation of Sexually Antagonistic Coevolution in Drosophila melanogaster

Promiscuity can drive the evolution of sexual conflict before and after mating occurs. Post mating, the male ejaculate can selfishly manipulate female physiology, leading to a chemical arms race between the sexes. Theory suggests that drift and sexually antagonistic coevolution can cause allopatric...

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Published inScientific reports Vol. 7; no. 1; pp. 3330 - 8
Main Authors Syed, Zeeshan Ali, Chatterjee, Martik, Samant, Manas Arun, Prasad, Nagaraj Guru
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 13.06.2017
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Abstract Promiscuity can drive the evolution of sexual conflict before and after mating occurs. Post mating, the male ejaculate can selfishly manipulate female physiology, leading to a chemical arms race between the sexes. Theory suggests that drift and sexually antagonistic coevolution can cause allopatric populations to evolve different chemical interactions between the sexes, thereby leading to postmating reproductive barriers and speciation. There is, however, little empirical evidence supporting this form of speciation. We tested this theory by creating an experimental evolutionary model of Drosophila melanogaster populations undergoing different levels of interlocus sexual conflict. We found that allopatric populations under elevated sexual conflict show assortative mating, indicating premating reproductive isolation. Further, these allopatric populations also show reduced copulation duration and sperm defense ability when mating happens between individuals across populations compared to that within the same population, indicating postmating prezygotic isolation. Sexual conflict can cause reproductive isolation in allopatric populations through the coevolution of chemical (postmating prezygotic) as well as behavioural (premating) interactions between the sexes. Thus, to our knowledge, we provide the first comprehensive evidence of postmating (as well as premating) reproductive isolation due to sexual conflict.
AbstractList Promiscuity can drive the evolution of sexual conflict before and after mating occurs. Post mating, the male ejaculate can selfishly manipulate female physiology, leading to a chemical arms race between the sexes. Theory suggests that drift and sexually antagonistic coevolution can cause allopatric populations to evolve different chemical interactions between the sexes, thereby leading to postmating reproductive barriers and speciation. There is, however, little empirical evidence supporting this form of speciation. We tested this theory by creating an experimental evolutionary model of Drosophila melanogaster populations undergoing different levels of interlocus sexual conflict. We found that allopatric populations under elevated sexual conflict show assortative mating, indicating premating reproductive isolation. Further, these allopatric populations also show reduced copulation duration and sperm defense ability when mating happens between individuals across populations compared to that within the same population, indicating postmating prezygotic isolation. Sexual conflict can cause reproductive isolation in allopatric populations through the coevolution of chemical (postmating prezygotic) as well as behavioural (premating) interactions between the sexes. Thus, to our knowledge, we provide the first comprehensive evidence of postmating (as well as premating) reproductive isolation due to sexual conflict.
Promiscuity can drive the evolution of sexual conflict before and after mating occurs. Post mating, the male ejaculate can selfishly manipulate female physiology, leading to a chemical arms race between the sexes. Theory suggests that drift and sexually antagonistic coevolution can cause allopatric populations to evolve different chemical interactions between the sexes, thereby leading to postmating reproductive barriers and speciation. There is, however, little empirical evidence supporting this form of speciation. We tested this theory by creating an experimental evolutionary model of Drosophila melanogaster populations undergoing different levels of interlocus sexual conflict. We found that allopatric populations under elevated sexual conflict show assortative mating, indicating premating reproductive isolation. Further, these allopatric populations also show reduced copulation duration and sperm defense ability when mating happens between individuals across populations compared to that within the same population, indicating postmating prezygotic isolation. Sexual conflict can cause reproductive isolation in allopatric populations through the coevolution of chemical (postmating prezygotic) as well as behavioural (premating) interactions between the sexes. Thus, to our knowledge, we provide the first comprehensive evidence of postmating (as well as premating) reproductive isolation due to sexual conflict.
Abstract Promiscuity can drive the evolution of sexual conflict before and after mating occurs. Post mating, the male ejaculate can selfishly manipulate female physiology, leading to a chemical arms race between the sexes. Theory suggests that drift and sexually antagonistic coevolution can cause allopatric populations to evolve different chemical interactions between the sexes, thereby leading to postmating reproductive barriers and speciation. There is, however, little empirical evidence supporting this form of speciation. We tested this theory by creating an experimental evolutionary model of Drosophila melanogaster populations undergoing different levels of interlocus sexual conflict. We found that allopatric populations under elevated sexual conflict show assortative mating, indicating premating reproductive isolation. Further, these allopatric populations also show reduced copulation duration and sperm defense ability when mating happens between individuals across populations compared to that within the same population, indicating postmating prezygotic isolation. Sexual conflict can cause reproductive isolation in allopatric populations through the coevolution of chemical (postmating prezygotic) as well as behavioural (premating) interactions between the sexes. Thus, to our knowledge, we provide the first comprehensive evidence of postmating (as well as premating) reproductive isolation due to sexual conflict.
ArticleNumber 3330
Author Prasad, Nagaraj Guru
Chatterjee, Martik
Syed, Zeeshan Ali
Samant, Manas Arun
Author_xml – sequence: 1
  givenname: Zeeshan Ali
  surname: Syed
  fullname: Syed, Zeeshan Ali
  organization: Indian Institute of Science Education and Research Mohali
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  givenname: Martik
  surname: Chatterjee
  fullname: Chatterjee, Martik
  organization: Indian Institute of Science Education and Research Mohali
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  givenname: Manas Arun
  surname: Samant
  fullname: Samant, Manas Arun
  organization: Indian Institute of Science Education and Research Mohali
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  givenname: Nagaraj Guru
  surname: Prasad
  fullname: Prasad, Nagaraj Guru
  email: prasad@iisermohali.ac.in
  organization: Indian Institute of Science Education and Research Mohali
BackLink https://www.ncbi.nlm.nih.gov/pubmed/28611437$$D View this record in MEDLINE/PubMed
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SSID ssj0000529419
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Snippet Promiscuity can drive the evolution of sexual conflict before and after mating occurs. Post mating, the male ejaculate can selfishly manipulate female...
Abstract Promiscuity can drive the evolution of sexual conflict before and after mating occurs. Post mating, the male ejaculate can selfishly manipulate female...
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StartPage 3330
SubjectTerms 631/181/2470
631/181/2475
631/181/759
64/24
Allopatric populations
Animal reproduction
Animals
Assortative mating
Biological Coevolution
Coevolution
Copulation
Drosophila melanogaster
Drosophila melanogaster - genetics
Female
Fish
Humanities and Social Sciences
Insects
Male
Mating
Mitochondrial DNA
Models, Genetic
multidisciplinary
Reproduction
Reproductive Isolation
Science
Science (multidisciplinary)
Sexual Behavior, Animal
Speciation
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Title Reproductive Isolation through Experimental Manipulation of Sexually Antagonistic Coevolution in Drosophila melanogaster
URI https://link.springer.com/article/10.1038/s41598-017-03182-1
https://www.ncbi.nlm.nih.gov/pubmed/28611437
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https://search.proquest.com/docview/1909749664
https://pubmed.ncbi.nlm.nih.gov/PMC5469766
https://doaj.org/article/ce0e01714dbe45c98fb9c850c224c6ec
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