Differentially expressed miRNAs in testes of dominant and subordinate Nile tilapia males and identification of oni-miR-499 as regulator of amh gene expression.

IF 2.4 4区 医学 Q2 DEVELOPMENTAL BIOLOGY
Rebecca Prause, Josephin Eckart, Jana Skrobanek, Michelle Thönnes, Frank Pfennig
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引用次数: 0

Abstract

Introduction: Gonadal development and reproduction are under the control of the endocrine system, which acts along the brain-pituitary-gonad (BPG) axis. Besides well-known regulators of the BPG axis, such as the gonadotropin-releasing hormone (GnRH), follicle-stimulating hormone (Fsh) and luteinizing hormone (Lh), the Anti-Müllerian hormone (Amh) came into the focus of research on the BPG axis. Amh is expressed differently in the gonads of dominant and subordinate Nile tilapia (Oreochromis niloticus) males and could be involved in the regulation of the differently developed gonads. In addition, the regulatory networks and the control of gene expression depend on microRNAs (miRNAs), an often not considered epigenetic mechanism in hormonal research.

Methods: We used a long-term, stable social hierarchy of Nile tilapia males as an experimental system to identify differentially expressed miRNAs in the testes of dominant and subordinate animals. A Dual Luciferase Reporter Assay and in vitro analysis of amh expression in primary testis cells were used to demonstrate predicted interactions.

Results: We identified 23 differentially expressed miRNAs in the testes of dominant and subordinate males and predicted the targets in the pools of differentially expressed genes. Using these data, we placed the identified GO terms and KEGG pathways in the context of differently developed gonads under social control. The most differentially expressed miRNA, oni-miR-499, is up-regulated in the testes of dominants and regulates amh expression.

Conclusion: We conclude that oni-miR-499 affects testis development via amh expression in Nile tilapia. Many miRNAs and biological processes identified in our study could be conserved mechanisms of testis development.

尼罗罗非鱼雄雄睾丸中mirna的差异表达及oni-miR-499作为amh基因表达调控因子的鉴定
性腺的发育和生殖受内分泌系统的控制,内分泌系统沿脑-垂体-性腺(BPG)轴起作用。除了众所周知的促性腺激素释放激素(GnRH)、促卵泡激素(Fsh)和黄体生成素(Lh)等BPG轴的调节因子外,抗勒氏激素(Amh)也成为BPG轴研究的重点。Amh在尼罗罗非鱼(Oreochromis niloticus)雄性雄性生殖腺中的表达不同,可能参与了不同发育性腺的调控。此外,调控网络和基因表达的控制依赖于microRNAs (miRNAs),这是激素研究中通常不被考虑的表观遗传机制。方法:我们使用长期稳定的尼罗罗非鱼雄性社会等级作为实验系统来鉴定优势和从属动物睾丸中差异表达的mirna。双荧光素酶报告试验和体外分析amh在原代睾丸细胞中的表达被用来证明预测的相互作用。结果:我们在优势雄性和从属雄性的睾丸中鉴定了23个差异表达的mirna,并预测了差异表达基因池中的靶点。利用这些数据,我们将确定的GO术语和KEGG途径置于社会控制下不同发育性腺的背景下。差异表达最多的miRNA, oni-miR-499,在显性的睾丸中上调并调节amh的表达。结论:我们认为oni-miR-499通过amh表达影响尼罗罗非鱼睾丸发育。在我们的研究中发现的许多mirna和生物学过程可能是睾丸发育的保守机制。
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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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