Key Laboratory of Tropical Marine Bio-Resources and Ecology, Guangdong Provincial Key Laboratory of Applied Marine Biology, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
Int J Mol Sci. 2024 May 21;25(11):5574. doi: 10.3390/ijms25115574.
The testis-specific double sex and mab-3-related transcription factor 1 () has long been recognized as a crucial player in sex determination across vertebrates, and its essential role in gonadal development and the regulation of spermatogenesis is well established. Here, we report the cloning of the key spermatogenesis-related cDNA, named , from the gonads of (), with a molecular weight of 41.93 kDa and an isoelectric point of 7.83 (pI). Our hypothesis is that machinery governs spermatogenesis and regulates gonadogenesis. RNAi-mediated knockdown revealed its critical role in hindering spermatogenesis and reducing expression levels in boring giant clams. A histological analysis showed structural changes, with normal sperm cell counts in the control group (ds-EGFP) but significantly lower concentrations of sperm cells in the experimental group (). transcripts during embryogenesis exhibited a significantly high expression pattern ( < 0.05) during the early zygote stage, and whole-embryo in-situ hybridization confirmed its expression pattern throughout embryogenesis. A qRT-PCR analysis of various reproductive stages revealed an abundant expression of in the gonads during the male reproductive stage. In-situ hybridization showed tissue-specific expression of , with a positive signal detected in male-stage gonadal tissues comprising sperm cells, while no signal was detected in other stages. Our study findings provide an initial understanding of the molecular machinery controlling spermatogenesis and its specificity in male-stage gonads of the key bivalve species, , and suggest that predominantly functions as a key regulator of spermatogenesis in giant clams.
睾丸特异性双性和 mab-3 相关转录因子 1 () 长期以来一直被认为是脊椎动物性别决定的关键因子,其在性腺发育和精子发生调控中的重要作用已得到证实。在这里,我们从 () 的性腺中克隆了关键精子发生相关 cDNA,命名为 ,分子量为 41.93 kDa,等电点为 7.83 (pI)。我们的假设是 机制控制精子发生并调节性腺发生。RNAi 介导的 敲低显示其在阻碍精子发生和减少钻孔巨蛤中的表达水平方面的关键作用。组织学分析显示结构发生变化,对照组(ds-EGFP)中正常精子细胞计数,但实验组()中精子细胞浓度明显降低。胚胎发生过程中的 转录本表现出显著高的表达模式(<0.05),在早期合子阶段,整体胚胎原位杂交证实了其在胚胎发生过程中的表达模式。对各种生殖阶段的 qRT-PCR 分析显示,在雄性生殖阶段, 在性腺中大量表达。原位杂交显示 组织特异性表达,在包含精子细胞的雄性阶段性腺组织中检测到阳性信号,而在其他阶段未检测到信号。我们的研究结果提供了对控制精子发生的 分子机制及其在关键双壳类物种 雄性性腺中的特异性的初步理解,并表明 主要作为巨蛤精子发生的关键调节剂发挥作用。