Intersex, Hermaphroditism, and Gonadal Plasticity in Vertebrates: Evolution of the Müllerian Duct and Amh/Amhr2 Signaling.

IF 8.7 1区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE Annual Review of Animal Biosciences Pub Date : 2019-02-15 Epub Date: 2018-10-10 DOI:10.1146/annurev-animal-020518-114955
Mateus Contar Adolfi, Rafael Takahiro Nakajima, Rafael Henrique Nóbrega, Manfred Schartl
{"title":"Intersex, Hermaphroditism, and Gonadal Plasticity in Vertebrates: Evolution of the Müllerian Duct and Amh/Amhr2 Signaling.","authors":"Mateus Contar Adolfi,&nbsp;Rafael Takahiro Nakajima,&nbsp;Rafael Henrique Nóbrega,&nbsp;Manfred Schartl","doi":"10.1146/annurev-animal-020518-114955","DOIUrl":null,"url":null,"abstract":"<p><p>In vertebrates, sex organs are generally specialized to perform a male or female reproductive role. Acquisition of the Müllerian duct, which gives rise to the oviduct, together with emergence of the Amh/Amhr2 system favored evolution of viviparity in jawed vertebrates. Species with high sex-specific reproductive adaptations have less potential to sex reverse, making intersex a nonfunctional condition. Teleosts, the only vertebrate group in which hermaphroditism evolved as a natural reproductive strategy, lost the Müllerian duct during evolution. They developed for gamete release complete independence from the urinary system, creating optimal anatomic and developmental preconditions for physiological sex change. The common and probably ancestral role of Amh is related to survival and proliferation of germ cells in early and adult gonads of both sexes rather than induction of Müllerian duct regression. The relationship between germ cell maintenance and sex differentiation is most evident in species in which Amh became the master male sex-determining gene.</p>","PeriodicalId":48953,"journal":{"name":"Annual Review of Animal Biosciences","volume":"7 ","pages":"149-172"},"PeriodicalIF":8.7000,"publicationDate":"2019-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1146/annurev-animal-020518-114955","citationCount":"55","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annual Review of Animal Biosciences","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1146/annurev-animal-020518-114955","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2018/10/10 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"AGRICULTURE, DAIRY & ANIMAL SCIENCE","Score":null,"Total":0}
引用次数: 55

Abstract

In vertebrates, sex organs are generally specialized to perform a male or female reproductive role. Acquisition of the Müllerian duct, which gives rise to the oviduct, together with emergence of the Amh/Amhr2 system favored evolution of viviparity in jawed vertebrates. Species with high sex-specific reproductive adaptations have less potential to sex reverse, making intersex a nonfunctional condition. Teleosts, the only vertebrate group in which hermaphroditism evolved as a natural reproductive strategy, lost the Müllerian duct during evolution. They developed for gamete release complete independence from the urinary system, creating optimal anatomic and developmental preconditions for physiological sex change. The common and probably ancestral role of Amh is related to survival and proliferation of germ cells in early and adult gonads of both sexes rather than induction of Müllerian duct regression. The relationship between germ cell maintenance and sex differentiation is most evident in species in which Amh became the master male sex-determining gene.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
脊椎动物的雌雄同体和性腺可塑性:腰管和Amh/Amhr2信号的进化。
在脊椎动物中,性器官通常是专门用于雄性或雌性生殖的角色。下颌椎管的形成,即输卵管的形成,以及Amh/Amhr2系统的出现,有利于有颌脊椎动物的胎生进化。具有高度性别特异性生殖适应性的物种性别逆转的可能性较小,使双性人成为一种无功能的状态。硬骨鱼是唯一一种将雌雄同体进化为自然繁殖策略的脊椎动物,在进化过程中失去了勒氏管。它们为配子的释放完全独立于泌尿系统而开发,为生理性别变化创造了最佳的解剖和发育前提条件。Amh的共同和可能的祖先作用与两性早期和成年性腺生殖细胞的存活和增殖有关,而不是诱导勒氏管退化。生殖细胞维持和性别分化之间的关系在Amh成为雄性主要性别决定基因的物种中最为明显。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Annual Review of Animal Biosciences
Annual Review of Animal Biosciences BIOTECHNOLOGY & APPLIED MICROBIOLOGY-ZOOLOGY
CiteScore
21.30
自引率
0.80%
发文量
31
期刊介绍: The Annual Review of Animal Biosciences is primarily dedicated to the fields of biotechnology, genetics, genomics, and breeding, with a special focus on veterinary medicine. This includes veterinary pathobiology, infectious diseases and vaccine development, and conservation and zoo biology. The publication aims to address the needs of scientists studying both wild and domesticated animal species, veterinarians, conservation biologists, and geneticists.
期刊最新文献
Comparative Genomics and Epigenomics of Transcriptional Regulation. Lipotoxicity and Oocyte Quality in Mammals: Pathogenesis, Consequences, and Reversibility. The Rhesus Macaque as an Animal Model for Human Nutrition: An Ecological-Evolutionary Perspective. A One Health Approach to Reducing Livestock Disease Prevalence in Developing Countries: Advances, Challenges, and Prospects. A Passion for Small Things and Staying Primed: My Career in Virology and Immunology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1