Zhao Ziduo, Wu Yuhui, Cheng Fufu, Wang Zhe, Geng Qingqing, Niu Yingjie, Zuo Qisheng, Zhang Yani
College of Animal Science and Technology, Yangzhou University, Jiangsu Province Key Laboratory of Animal Breeding and Molecular Design, Yangzhou 225009 Jiangsu, PR China; Joint International Research Laboratory of Agriculture and Agri-Product Safety of Ministry of Education of China, Yangzhou University, Yangzhou 225009 Jiangsu, PR China.
College of Animal Science and Technology, Yangzhou University, Jiangsu Province Key Laboratory of Animal Breeding and Molecular Design, Yangzhou 225009 Jiangsu, PR China; Joint International Research Laboratory of Agriculture and Agri-Product Safety of Ministry of Education of China, Yangzhou University, Yangzhou 225009 Jiangsu, PR China.
Poult Sci. 2025 Feb;104(2):104763. doi: 10.1016/j.psj.2024.104763. Epub 2025 Jan 6.
This study investigates the role of histone acetylation in the differentiation of chicken embryonic stem cells (ESCs) into primordial germ cells (PGCs). Transcriptomic sequencing was used to analyze differentially expressed genes during this differentiation process, with functional annotation identifying genes associated with histone acetylation. To explore the role of acetylation, acetate and an acetyltransferase inhibitor (ANAC) were added to the ESCs induction medium. Transcriptomic analysis revealed that during ESCs differentiation into PGCs, genes involved in histone acetyltransferase activity were upregulated, while those associated with histone deacetylase activity were downregulated. Functional enrichment analysis indicated these genes are involved in pathways critical for germ cell differentiation, underscoring their importance in avian reproductive biology. Quantitative real-time PCR (qRT-PCR) confirmed significant differential expression of HAT8 and HDAC10 between ESCs and PGCs (P < 0.01). The acetate treatment group exhibited a significantly higher number of embryoid bodies and elevated expression levels of CVH, C-KIT, and NANOS3 compared to the ANAC group (P < 0.01). Furthermore, indirect immunofluorescence and flow cytometry demonstrated a significantly higher proportion of DDX4-positive cells in the acetate group (P < 0.01). These findings provide preliminary evidence that histone acetylation regulates chicken PGCs formation, offering a theoretical framework for the epigenetic induction of PGCs in vitro. This study enhances our understanding of the molecular mechanisms underlying PGCs development in poultry and contributes to advancements in avian reproductive technologies and genetic conservation.
本研究调查了组蛋白乙酰化在鸡胚胎干细胞(ESCs)向原始生殖细胞(PGCs)分化过程中的作用。利用转录组测序分析该分化过程中差异表达的基因,并通过功能注释鉴定与组蛋白乙酰化相关的基因。为了探究乙酰化的作用,将乙酸盐和一种乙酰转移酶抑制剂(ANAC)添加到ESCs诱导培养基中。转录组分析显示,在ESCs向PGCs分化过程中,参与组蛋白乙酰转移酶活性的基因上调,而与组蛋白去乙酰化酶活性相关的基因下调。功能富集分析表明,这些基因参与了对生殖细胞分化至关重要的信号通路,突出了它们在禽类生殖生物学中的重要性。定量实时PCR(qRT-PCR)证实了ESCs和PGCs之间HAT8和HDAC10存在显著差异表达(P < 0.01)。与ANAC组相比,乙酸盐处理组的类胚体数量显著更多,且CVH、C-KIT和NANOS3的表达水平升高(P < 0.01)。此外,间接免疫荧光和流式细胞术显示,乙酸盐组中DDX4阳性细胞的比例显著更高(P < 0.01)。这些发现提供了初步证据,表明组蛋白乙酰化调节鸡PGCs的形成,为体外PGCs的表观遗传诱导提供了理论框架。本研究增进了我们对家禽PGCs发育分子机制的理解,并有助于推进禽类生殖技术和遗传保护。