Smad4和FoxH1可能相互作用调控稻田鳗(Monopterus albus)卵巢中的cyp19a1a启动子。

IF 4.9 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Qiqi Chen, Deying Yang, Mingqiang Chen, Jinxin Xiong, Junjie Huang, Wenxiang Ding, Kuo Gao, Bolin Lai, Li Zheng, Ziting Tang, Mingwang Zhang, Taiming Yan, Zhi He
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引用次数: 0

摘要

背景:Cyp19a1a是雄激素转化为雌激素途径中的一个关键酶,受TGF-β信号调控。Smad4和FoxH1是TGF-β信号传导的下游效应器,可能在M. albus卵巢发育过程中发挥重要作用:方法:利用qRT-PCR和免疫荧光技术研究了Smad4和FoxH1的表达模式,然后通过qRT-PCR检测了卵巢与FSH体外培养后Smad4和FoxH1的变化,并通过双荧光素酶报告实验分析了Smad4和FoxH1对cyp19a1a转录的调控作用:结果:我们发现Smad4编码一个449个氨基酸的假定蛋白,含有该蛋白家族的三个典型保守结构域。Smad4和foxh1在卵巢发育过程中和FSH孵育后表现出相似的表达模式,皮尔逊系数分别为0.873和0.63-0.81。此外,在卵黄形成的中后期,Smad4、FoxH1和Cyp19a1a共定位在卵巢的颗粒细胞和theca细胞中。Smad4通过cyp19a1a启动子中的SBE1(- 1372/-1364)和SBE2(- 415/-407)抑制cyp19a1a的活性,而突变SBE1或SBE2可恢复cyp19a1a启动子的活性。Smad4和FoxH1的共重表达显著降低了cyp19a1a启动子的活性:本研究为了解转录因子Smad4和FoxH1在卵巢发育中的潜在功能以及白僵菌cyp19a1a的转录调控机制提供了新的视角,将揭示Smad4/FoxH1介导的TGF-β信号在繁殖过程中的作用以及cyp19a1a的调控机制。由cyp19a1a编码的芳香化酶参与卵巢发育,并对远东鱼类白鲑鱼的卵子质量和性别比例起着重要作用。对cyp19a1a转录调控的研究有助于了解其在卵巢发育中的作用。之前的研究表明,FoxH1抑制cyp19a1a的转录。在本研究中,Smad4被证实是cyp19a1a的转录抑制因子,并且Smad4还可能与FoxH1协调抑制cyp19a1a的转录。目前,我们为转录因子Smad4和FoxH1在远洋鱼类卵巢中对cyp19a1a的转录调控提供了一个新的视角。未来,我们将进一步研究Smad4和FoxH1的调控网络,并应用基因编辑技术筛选cyp191a1a基因的特异性调控因子,从而改变雌性周期,调节产卵的性别比例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Smad4 and FoxH1 potentially interact to regulate cyp19a1a promoter in the ovary of ricefield eel (Monopterus albus).

Background: Cyp19a1a is a key enzyme in the pathway that converts androgens into estrogen and is regulated by TGF-β signaling. Smad4 and FoxH1 are downstream effectors of TGF-β signaling and may play important roles in ovarian development in M. albus.

Methods: We investigated the expression pattern of the Smad4 and FoxH1 using qRT‒PCR and immunofluorescence, then tested the changes of smad4 and foxh1 by qRT‒PCR after ovary incubation with FSH in vitro, and analysed the regulation of cyp19a1a transcription by Smad4 and FoxH1 by dual-luciferase reporter assays.

Results: We found that Smad4 encoded a putative protein of 449 amino acids and harbored the three conserved domains typical of this protein family. Smad4 and foxh1 exhibited similar expression patterns during ovarian development and after FSH incubation, with Pearson's coefficients of 0.873 and 0.63-0.81, respectively. Furthermore, Smad4, FoxH1 and Cyp19a1a colocalized in the granulosa cells and theca cells of ovaries during the mid-to-late vitellogenic stage. Smad4 repressed cyp19a1a activity via SBE1 (- 1372/-1364) and SBE2 (- 415/-407) in the cyp19a1a promoter, whereas mutating SBE1 or SBE2 restored cyp19a1a promoter activity. Co-overexpression of Smad4 and FoxH1 significantly reduced cyp19a1a promoter activity.

Conclusions: This study provides new insights into the potential functions of transcription factors Smad4 and FoxH1 in ovarian development and the transcriptional regulation mechanism of cyp19a1a in M. albus, which will reveal Smad4/FoxH1-mediated TGF-β signaling in reproduction and the regulation of the cyp19a1a. Aromatase, encoded by cyp19a1a, is involved in ovarian development and plays an important role in the quality of eggs, as well the sex ratio, of the teleost fish, M. albus. The research on the transcriptional regulation of cyp19a1a has contributed to the understanding of its role in ovarian development. In previous study, it was shown that FoxH1 inhibits cyp19a1a transcription. In the present study, Smad4 was confirmed as a cyp19a1a transcriptional repressor and Smad4 may also coordinate with FoxH1 to repress cyp19a1a transcription. At present, we provide a new perspective for the transcriptional regulation of cyp19a1a by transcription factors Smad4 and FoxH1 in teleost fish ovary. In the future, the regulatory networks of Smad4 and FoxH1 will be further studied and the gene editing technology will be applied to screen specific regulatory factors of cyp191a1a gene, so as to alter the female cycle and modulate the sex ratio of the eggs production.

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来源期刊
Biology of Sex Differences
Biology of Sex Differences ENDOCRINOLOGY & METABOLISM-GENETICS & HEREDITY
CiteScore
12.10
自引率
1.30%
发文量
69
审稿时长
14 weeks
期刊介绍: Biology of Sex Differences is a unique scientific journal focusing on sex differences in physiology, behavior, and disease from molecular to phenotypic levels, incorporating both basic and clinical research. The journal aims to enhance understanding of basic principles and facilitate the development of therapeutic and diagnostic tools specific to sex differences. As an open-access journal, it is the official publication of the Organization for the Study of Sex Differences and co-published by the Society for Women's Health Research. Topical areas include, but are not limited to sex differences in: genomics; the microbiome; epigenetics; molecular and cell biology; tissue biology; physiology; interaction of tissue systems, in any system including adipose, behavioral, cardiovascular, immune, muscular, neural, renal, and skeletal; clinical studies bearing on sex differences in disease or response to therapy.
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