Decoding Dmrt1: Insights into vertebrate sex determination and gonadal sex differentiation.

IF 2.1 3区 生物学 Q3 ECOLOGY
Barbora Augstenová, Wen-Juan Ma
{"title":"Decoding Dmrt1: Insights into vertebrate sex determination and gonadal sex differentiation.","authors":"Barbora Augstenová, Wen-Juan Ma","doi":"10.1093/jeb/voaf031","DOIUrl":null,"url":null,"abstract":"<p><p>The Dmrt gene family is characterized by a conserved DM domain. It includes nine genes in vertebrates and is crucial to sex determination and sexual differentiation. Dmrt1 is pivotal in testis formation and function by interacting with genes crucial for Sertoli cell differentiation, such as Sox9. Dmrt1, or Sox9, forms a conserved antagonistic interaction with Foxl2 (crucial for ovarian formation) across mammals. Across 128 vertebrate species, Dmrt1 exhibits sexually dimorphic expression, prior to and during gonadal sex differentiation and in adult testes, implicating its role in master regulation of sex determination and gonadal sex differentiation. Dmrt1 emerges as a master/upstream sex-determining gene in one fish, frog, chicken and turtle, with candidacy in 12 other vertebrate species. Recent studies suggest epigenetic regulation of Dmrt1 in its promoter methylation, and transposable element insertion introducing epigenetic modification to cis-regulatory elements of Dmrt1, alongside non-coding RNA involvement, in a wide spectrum of sex-determining mechanisms ranging from genetic factors, to interactions between genetic factors with the environment, to solely environmental factors. Additionally, alternative splicing of Dmrt1 was found in all major vertebrate groups except amphibians. Dmrt1 has evolved many lineage-specific isoforms (ranging from 2 to 10), and various isoforms showed sex, tissue or development-specific expression, which is in contrast to the highly conserved sex-specific splicing of its homolog Dsx across insects. Future research should focus on understanding the molecular basis of environmental sex determination from a broader taxon, and the molecular basis of epigenetic regulation. It is also essential to understand why and how multiple alternative splicing variants of Dmrt1 evolve in vertebrates, the specific roles each isoform plays in sex determination and gonadal sex differentiation, as well as the significant differences in the molecular mechanisms and functions of alternative splicing between Dmrt1 in vertebrates and Dsx in insects. Understanding the differences could provide deeper insights into the evolution of sex-determining mechanisms between vertebrates and insects.</p>","PeriodicalId":50198,"journal":{"name":"Journal of Evolutionary Biology","volume":" ","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2025-03-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Evolutionary Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/jeb/voaf031","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ECOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The Dmrt gene family is characterized by a conserved DM domain. It includes nine genes in vertebrates and is crucial to sex determination and sexual differentiation. Dmrt1 is pivotal in testis formation and function by interacting with genes crucial for Sertoli cell differentiation, such as Sox9. Dmrt1, or Sox9, forms a conserved antagonistic interaction with Foxl2 (crucial for ovarian formation) across mammals. Across 128 vertebrate species, Dmrt1 exhibits sexually dimorphic expression, prior to and during gonadal sex differentiation and in adult testes, implicating its role in master regulation of sex determination and gonadal sex differentiation. Dmrt1 emerges as a master/upstream sex-determining gene in one fish, frog, chicken and turtle, with candidacy in 12 other vertebrate species. Recent studies suggest epigenetic regulation of Dmrt1 in its promoter methylation, and transposable element insertion introducing epigenetic modification to cis-regulatory elements of Dmrt1, alongside non-coding RNA involvement, in a wide spectrum of sex-determining mechanisms ranging from genetic factors, to interactions between genetic factors with the environment, to solely environmental factors. Additionally, alternative splicing of Dmrt1 was found in all major vertebrate groups except amphibians. Dmrt1 has evolved many lineage-specific isoforms (ranging from 2 to 10), and various isoforms showed sex, tissue or development-specific expression, which is in contrast to the highly conserved sex-specific splicing of its homolog Dsx across insects. Future research should focus on understanding the molecular basis of environmental sex determination from a broader taxon, and the molecular basis of epigenetic regulation. It is also essential to understand why and how multiple alternative splicing variants of Dmrt1 evolve in vertebrates, the specific roles each isoform plays in sex determination and gonadal sex differentiation, as well as the significant differences in the molecular mechanisms and functions of alternative splicing between Dmrt1 in vertebrates and Dsx in insects. Understanding the differences could provide deeper insights into the evolution of sex-determining mechanisms between vertebrates and insects.

求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Evolutionary Biology
Journal of Evolutionary Biology 生物-进化生物学
CiteScore
4.20
自引率
4.80%
发文量
152
审稿时长
3-6 weeks
期刊介绍: It covers both micro- and macro-evolution of all types of organisms. The aim of the Journal is to integrate perspectives across molecular and microbial evolution, behaviour, genetics, ecology, life histories, development, palaeontology, systematics and morphology.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信