Chen Shijian, Liu Wenjun, Yang Chen, Li Xiujin, Shen Xu, Jiang Danli, Huang Yunmao, Tian Yunbo
Zhongkai University of Agriculture and Engineering, Guangdong Guangzhou, China.
Guangdong Province Key Laboratory of Waterfowl Healthy Breeding, Guangdong Guangzhou, China.
Anim Reprod. 2021 Jul 19;18(2):e20210036. doi: 10.1590/1984-3143-AR2021-0036. eCollection 2021.
The mechanisms by which GnIH regulates the steroid synthesis pathway in duck granulosa cells remain poorly understood. In this study, we measured steroid hormone secretion by ELISA and reproduction-associated gene expression by quantitative real-time Polymerase Chain Reaction (qPCR) in duck granulosa cells treated with different concentrations of GnIH (0, 0.1, 1, 10, and 100 ng/mL) for 24 h. The genome-wide expression profiles of GnIH-treated cells (0 and 10 ng/mL) were evaluated by high-throughput RNA sequencing. Compared with untreated cells, the secretion of the steroid hormones E2, E1, P4, and T was downregulated, with that of E1 and P4 reaching statistical significance (<0.05); in contrast, the secretion of ACV and INH was significantly upregulated (<0.05) after treatment with 10 and 100 ng/mL GnIH. The expression of encoding steroidogenic proteins and enzymes genes (, , , , and ) and encoding gonadotropin receptors genes (, ) were significantly declined (<0.05) in the 10 and 100 ng/mL GnIH treatments. Transcriptome sequencing identified 348 differentially expressed genes (DEGs), including 253 upregulated and 95 downregulated genes. The DEGs were mainly involved in cell growth and death, immune response, and steroid biosynthesis pathways. We identified four novel DEGs (, , , and ) with key roles in the regulation of steroid hormone biosynthesis. Our study revealed changes in gonadal steroid hormone secretion and steroid biosynthesis pathway-related gene expression in duck granulosa cells under the inhibitory effect of GnIH. These data contribute to our understanding of the molecular and genetic mechanisms underlying reproduction in ducks.
促性腺激素抑制激素(GnIH)调节鸭颗粒细胞类固醇合成途径的机制仍不清楚。在本研究中,我们通过酶联免疫吸附测定(ELISA)测量了用不同浓度的GnIH(0、0.1、1、10和100 ng/mL)处理24小时的鸭颗粒细胞中类固醇激素的分泌,并通过定量实时聚合酶链反应(qPCR)检测了与繁殖相关基因的表达。通过高通量RNA测序评估了GnIH处理细胞(0和10 ng/mL)的全基因组表达谱。与未处理的细胞相比,类固醇激素E2、E1、P4和T的分泌下调,其中E1和P4的分泌达到统计学显著性(<0.05);相反,在用10和100 ng/mL GnIH处理后,ACV和INH的分泌显著上调(<0.05)。在10和100 ng/mL GnIH处理中,编码类固醇生成蛋白和酶的基因(、、、和)以及编码促性腺激素受体的基因(、)的表达显著下降(<0.05)。转录组测序鉴定出348个差异表达基因(DEG),包括253个上调基因和95个下调基因。这些DEG主要参与细胞生长和死亡、免疫反应以及类固醇生物合成途径。我们鉴定出四个在类固醇激素生物合成调节中起关键作用的新DEG(、、、和)。我们的研究揭示了在GnIH的抑制作用下,鸭颗粒细胞中性腺类固醇激素分泌和类固醇生物合成途径相关基因表达的变化。这些数据有助于我们理解鸭繁殖的分子和遗传机制。