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
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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.

解码Dmrt1:对脊椎动物性别决定和性腺性别分化的见解。
Dmrt基因家族的特征是一个保守的DM结构域。它包括脊椎动物中的9个基因,对性别决定和性别分化至关重要。Dmrt1通过与支持细胞分化的关键基因(如Sox9)相互作用,在睾丸形成和功能中起关键作用。Dmrt1或Sox9在哺乳动物中与Foxl2(对卵巢形成至关重要)形成保守的拮抗相互作用。在128种脊椎动物中,Dmrt1在性腺性别分化之前和期间以及成年睾丸中表现出两性二态表达,暗示其在性别决定和性腺性别分化的主要调控中发挥作用。Dmrt1在一种鱼、青蛙、鸡和海龟中作为主/上游性别决定基因出现,在其他12种脊椎动物中也有候选基因。最近的研究表明,Dmrt1启动子甲基化的表观遗传调控,以及转座元件插入引入表观遗传修饰的Dmrt1顺式调控元件,以及非编码RNA的参与,在广泛的性别决定机制中,从遗传因素到遗传因素与环境之间的相互作用,再到单独的环境因素。此外,Dmrt1的选择性剪接在除两栖动物外的所有主要脊椎动物群体中都被发现。Dmrt1已经进化出许多谱系特异性亚型(从2到10种不等),并且各种亚型表现出性别、组织或发育特异性表达,这与其同源物Dsx在昆虫中高度保守的性别特异性剪接形成鲜明对比。今后的研究应着眼于从更广泛的分类单元理解环境性别决定的分子基础,以及表观遗传调控的分子基础。了解Dmrt1的多种选择性剪接变体在脊椎动物中进化的原因和方式,每个亚型在性别决定和性腺性别分化中所起的具体作用,以及Dmrt1在脊椎动物和Dsx在昆虫中选择性剪接的分子机制和功能的显着差异也是必不可少的。了解这些差异可以更深入地了解脊椎动物和昆虫之间性别决定机制的进化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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.
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