橙斑石斑鱼piwi1同源基因的鉴定及其在生殖细胞谱系中的表达模式

IF 2.2 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ling Qu , Kunlun Xiang
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引用次数: 0

摘要

原性橘斑石斑鱼(Epinephelus coioides)是一种序性雌雄同体硬鱼,依靠生殖细胞发育的动态调节和性别逆转机制来实现生殖可塑性。piwi基因家族是后生动物生殖细胞发育和转座子沉默的关键,但在雌雄同体物种中仍然缺乏特征。在这里,我们研究了piwi1在橙斑石斑鱼(e.c oioides)中的同系物Ecpiwi1,以阐明其在生殖细胞命运决定和性别逆转中的作用。我们克隆了一个3084 bp的Ecpiwi1 cDNA,编码一个含有保守PAZ和PIWI结构域的855个氨基酸的蛋白,与脊椎动物PIWI蛋白在系统发育上聚类。Real-time PCR结果显示,Ecpiwi1 mRNA在从卵巢到睾丸的性别转换过程中表达水平升高。原位杂交和免疫组织化学的空间表达分析表明,Ecpiwi1定位于卵原细胞、卵黄前卵母细胞和精原细胞-精母细胞过渡区。在自然和17α-甲基睾酮(MT)诱导的性别逆转过程中,Ecpiwi1 mRNA在性别逆转过程中表现出进行性上调。值得注意的是,与自然性别变化相比,MT处理性腺显示出相同的Ecpiwi1表达动态和亚细胞定位模式,验证了MT诱导模型。这些发现证实了Ecpiwi1作为生殖系特异性调节因子,在雌雄同体中协调卵子发生、精子发生和性别逆转。外源雄激素诱导下的保守表达模式使Ecpiwi1成为硬骨鱼生殖系干细胞研究的一个强有力的分子标记,并促进了我们对雌雄同体硬骨鱼生殖可塑性的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of a piwi1 homologue gene in the orange-spotted grouper (Epinephelus coioides) and its expression pattern in the germ cell lineage
The protogynous orange-spotted grouper (Epinephelus coioides), a sequentially hermaphroditic teleost, relies on dynamic regulation of germ cell development and sex reversal mechanisms to achieve reproductive plasticity. The piwi gene family, pivotal for germ cell development and transposon silencing across metazoans, remains poorly characterized in hermaphroditic species. Here, we investigate Ecpiwi1, a piwi1 homologue in the orange-spotted grouper (E. coioides), to elucidate its role in germ cell fate determination and sex reversal. We cloned a 3084-bp Ecpiwi1 cDNA encoding an 855-amino-acid protein containing conserved PAZ and PIWI domains, phylogenetically clustering with vertebrate Piwi proteins. Real-time PCR showed that the expression level of Ecpiwi1 mRNA increases during sex reversal, transitioning from ovary to testis. Spatial expression analysis by in situ hybridization and immunohistochemistry demonstrated Ecpiwi1 localization to oogonia, previtellogenic oocytes, and spermatogonia-spermatocyte transition zones. During natural and 17α-methyltestosterone (MT)-induced sex reversal, Ecpiwi1 mRNA exhibited progressive upregulation during sex reversal. Notably, MT-treated gonads showed identical Ecpiwi1 expression dynamics and subcellular localization patterns compared to natural sex change, validating the MT induction model. These findings establish Ecpiwi1 as a germline-specific regulator coordinating oogenesis, spermatogenesis, and sex reversal in protogynous hermaphrodites. The conserved expression patterns under exogenous androgen induction position Ecpiwi1 as a robust molecular marker for teleost germline stem cell studies and advance our understanding of reproductive plasticity in hermaphroditic teleosts.
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来源期刊
Biochemistry and Biophysics Reports
Biochemistry and Biophysics Reports Biochemistry, Genetics and Molecular Biology-Biophysics
CiteScore
4.60
自引率
0.00%
发文量
191
审稿时长
59 days
期刊介绍: Open access, online only, peer-reviewed international journal in the Life Sciences, established in 2014 Biochemistry and Biophysics Reports (BB Reports) publishes original research in all aspects of Biochemistry, Biophysics and related areas like Molecular and Cell Biology. BB Reports welcomes solid though more preliminary, descriptive and small scale results if they have the potential to stimulate and/or contribute to future research, leading to new insights or hypothesis. Primary criteria for acceptance is that the work is original, scientifically and technically sound and provides valuable knowledge to life sciences research. We strongly believe all results deserve to be published and documented for the advancement of science. BB Reports specifically appreciates receiving reports on: Negative results, Replication studies, Reanalysis of previous datasets.
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