Rachel C Thayer, Elizabeth S Polston, Giovanni Hanna, David J Begun
{"title":"没有证据表明果蝇生殖道转录组存在性拮抗性共同进化。","authors":"Rachel C Thayer, Elizabeth S Polston, Giovanni Hanna, David J Begun","doi":"10.1093/molbev/msaf210","DOIUrl":null,"url":null,"abstract":"<p><p>Drosophila seminal fluid proteins (SFPs) are often cited as an example of interlocus sexual conflict, wherein the proteins increase male fitness while decreasing female fitness, spurring recurring female counter-adaptations and rapid molecular evolution. This model predicts that male-expressed genetic variation in the accessory gland, which produces seminal fluid, should generate counter-evolving genetic pathways in females, resulting in sexual coevolution. Using a trio of D. melanogaster populations exhibiting substantial SFP expression divergence due to recent selection, we test for coevolution in the female post-mating transcriptome in the lower reproductive tract and head. Contrasting predictions of sexual antagonism, female post-mating gene expression is indifferent to male population of origin. Instead, our results better support the alternative hypotheses that environmental variation is the source of selection on male SFP gene expression and that population differentiation in the female post-mating transcriptome is generated by female-expressed genotypic differentiation.</p>","PeriodicalId":18730,"journal":{"name":"Molecular biology and evolution","volume":" ","pages":""},"PeriodicalIF":5.3000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12449178/pdf/","citationCount":"0","resultStr":"{\"title\":\"No Evidence of Sexually Antagonistic Coevolution in Drosophila Reproductive Tract Transcriptomes.\",\"authors\":\"Rachel C Thayer, Elizabeth S Polston, Giovanni Hanna, David J Begun\",\"doi\":\"10.1093/molbev/msaf210\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Drosophila seminal fluid proteins (SFPs) are often cited as an example of interlocus sexual conflict, wherein the proteins increase male fitness while decreasing female fitness, spurring recurring female counter-adaptations and rapid molecular evolution. This model predicts that male-expressed genetic variation in the accessory gland, which produces seminal fluid, should generate counter-evolving genetic pathways in females, resulting in sexual coevolution. Using a trio of D. melanogaster populations exhibiting substantial SFP expression divergence due to recent selection, we test for coevolution in the female post-mating transcriptome in the lower reproductive tract and head. Contrasting predictions of sexual antagonism, female post-mating gene expression is indifferent to male population of origin. Instead, our results better support the alternative hypotheses that environmental variation is the source of selection on male SFP gene expression and that population differentiation in the female post-mating transcriptome is generated by female-expressed genotypic differentiation.</p>\",\"PeriodicalId\":18730,\"journal\":{\"name\":\"Molecular biology and evolution\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":5.3000,\"publicationDate\":\"2025-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12449178/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular biology and evolution\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1093/molbev/msaf210\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular biology and evolution","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/molbev/msaf210","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
No Evidence of Sexually Antagonistic Coevolution in Drosophila Reproductive Tract Transcriptomes.
Drosophila seminal fluid proteins (SFPs) are often cited as an example of interlocus sexual conflict, wherein the proteins increase male fitness while decreasing female fitness, spurring recurring female counter-adaptations and rapid molecular evolution. This model predicts that male-expressed genetic variation in the accessory gland, which produces seminal fluid, should generate counter-evolving genetic pathways in females, resulting in sexual coevolution. Using a trio of D. melanogaster populations exhibiting substantial SFP expression divergence due to recent selection, we test for coevolution in the female post-mating transcriptome in the lower reproductive tract and head. Contrasting predictions of sexual antagonism, female post-mating gene expression is indifferent to male population of origin. Instead, our results better support the alternative hypotheses that environmental variation is the source of selection on male SFP gene expression and that population differentiation in the female post-mating transcriptome is generated by female-expressed genotypic differentiation.
期刊介绍:
Molecular Biology and Evolution
Journal Overview:
Publishes research at the interface of molecular (including genomics) and evolutionary biology
Considers manuscripts containing patterns, processes, and predictions at all levels of organization: population, taxonomic, functional, and phenotypic
Interested in fundamental discoveries, new and improved methods, resources, technologies, and theories advancing evolutionary research
Publishes balanced reviews of recent developments in genome evolution and forward-looking perspectives suggesting future directions in molecular evolution applications.