北梭鱼抗 lererian激素受体2型(amhrII)基因失活导致雄性向雌性的性别逆转。

IF 2.4 4区 医学 Q2 DEVELOPMENTAL BIOLOGY Sexual Development Pub Date : 2022-01-01 DOI:10.1159/000521003
Qiaowei Pan, Amaury Herpin, Yann Guiguen
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引用次数: 2

摘要

背景:抗勒氏激素(Amh)通路对硬骨鱼的性发育至关重要。一种雄性特异性的抗m勒氏激素(amhby)重复基因先前被确定为北梭子鱼(Esox lucius)的主性别决定基因。然而,其假定的同源受体,即抗勒氏杆菌激素受体2型(amhrII)在该物种中的作用尚不清楚。目的:研究amhrII在北梭子鱼性发育过程中的作用。方法:利用crispr - cas9介导的基因敲除策略,生成amhrII外显子9缺失的稳定突变体,使amhrII蛋白失活。结果:北梭鱼amhrII基因失活导致高水平的雌雄转换。结论:该结果表明amhrII在硬骨鱼雄性分化网络中起着重要的调节作用,并支持amhrII在硬骨鱼性别分化网络中的保守调节作用。
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Inactivation of the Anti-Müllerian Hormone Receptor Type 2 (amhrII) Gene in Northern Pike (Esox lucius) Results in Male-To-Female Sex Reversal.

Background: The anti-müllerian hormone (Amh) pathway is crucial for sexual development in teleosts. A male-specific duplicate of anti-müllerian hormone (amhby) was previously identified as the northern pike (Esox lucius) master sex determination gene. However, the role of its putative cognate receptor, i.e., the anti-müllerian hormone receptor type 2 (amhrII) was unclear in this species.

Objective: Here, we investigated the role of amhrII during sexual development of northern pike.

Method: We generated stable mutants with deletions in exon 9 of amhrII, inactivating the AmhrII protein using a CRISPR-Cas9-mediated gene knockout strategy.

Result: The inactivation of amhrII in northern pike results in a high level of male-to-female sex reversal.

Conclusion: This result demonstrates that amhrII is necessary for male sexual development in northern pike and supports the idea that AmhrII is a conserved regulator of the teleosts sex differentiation network.

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来源期刊
Sexual Development
Sexual Development 生物-发育生物学
CiteScore
4.00
自引率
4.30%
发文量
25
审稿时长
>12 weeks
期刊介绍: Recent discoveries in experimental and clinical research have led to impressive advances in our knowledge of the genetic and environmental mechanisms governing sex determination and differentiation, their evolution as well as the mutations or endocrine and metabolic abnormalities that interfere with normal gonadal development. ‘Sexual Development’ provides a unique forum for this rapidly expanding field. Its broad scope covers all aspects of genetics, molecular biology, embryology, endocrinology, evolution and pathology of sex determination and differentiation in humans and animals. It publishes high-quality original research manuscripts, review articles, short reports, case reports and commentaries. An internationally renowned and multidisciplinary editorial team of three chief editors, ten prominent scientists serving as section editors, and a distinguished panel of editorial board members ensures fast and author-friendly editorial processing and peer reviewing.
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