gsdfb, But Not the Isoforms gsdfa1 and gsdfa2, Is Up-Regulated During the Male Program and Repressed by Estrogens in Siberian Sturgeon

IF 2.6 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
German Benech-Correa, André Lasalle, Fréderic Brunet, Denise Vizziano-Cantonnet
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引用次数: 0

Abstract

The search for male-biased genes that may drive sexual differentiation in sturgeon gonadal tissue has remained largely fruitless until now. This study explored the presence, expression, and sexual steroid regulation of gonadal soma-derived factor (Gsdf) in Siberian sturgeon (Acipenser baerii). Three sequences compatible with the protein-coding gene gsdf were identified in a Siberian sturgeon gonadal transcriptome database. The phylogenetic analysis shows the presence of two paralogues gsdfa and gsdfb, and two clearly identifiable gsdfa isoforms (gsdfa1 and gsdfa2). gsdfa was expressed in sex-undifferentiated gonads, brain, hypophysis, heart, interrenal, intestine, liver, stomach, embryos and larvae, while gsdfb was specific to the gonads. gsdfb showed significantly higher expression in genetically sexed males during late stage of sex differentiation. In contrast, gsdfa1 and gsdfa2 showed similar gonadal expression levels in both sexes. In terms of sensitivity to sexual steroids, only gsdfb was repressed significantly and in a dose-dependent manner by estrogens. Taken together, these results indicate both that gsdfb is part of the male gonadal differentiation pathway in sturgeon and that its repression by estrogens is fundamental for female development.

gsdfb,而不是gsdfa1和gsdfa2同工型,在雄性程序中上调,受雌激素抑制。
迄今为止,对可能驱动鲟鱼性腺组织性别分化的雄性偏倚基因的研究基本上没有结果。本研究探讨了性腺体细胞衍生因子(Gsdf)在西伯利亚鲟鱼(Acipenser baerii)体内的存在、表达及性类固醇调控。在西伯利亚鲟鱼性腺转录组数据库中鉴定出3个与蛋白质编码基因gsdf兼容的序列。系统发育分析显示,gsdfa和gsdfb有两个同源物,gsdfa1和gsdfa2有两个同源物。Gsdfa在性腺、脑、垂体、心脏、肾间、肠、肝、胃、胚胎和幼虫中均有表达,而GSDFB则特异于性腺。GSDFB在性别分化后期在遗传性别雄性中表达显著升高。相比之下,gsdfa1和gsdfa2在两性中的性腺表达水平相似。在对性类固醇的敏感性方面,只有gsdfb被雌激素显著抑制,且呈剂量依赖性。综上所述,这些结果表明gsdfb是鲟鱼雄性性腺分化途径的一部分,并且雌激素对其的抑制是雌性发育的基础。
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来源期刊
CiteScore
5.20
自引率
0.00%
发文量
78
审稿时长
6-12 weeks
期刊介绍: Molecular Reproduction and Development takes an integrated, systems-biology approach to understand the dynamic continuum of cellular, reproductive, and developmental processes. This journal fosters dialogue among diverse disciplines through primary research communications and educational forums, with the philosophy that fundamental findings within the life sciences result from a convergence of disciplines. Increasingly, readers of the Journal need to be informed of diverse, yet integrated, topics impinging on their areas of interest. This requires an expansion in thinking towards non-traditional, interdisciplinary experimental design and data analysis.
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