Zuo Qisheng, Zhou Jing, Wang Man, Zhang Yani, Chen Guohong, Li Bichun
Key Laboratory of Animal Breeding Reproduction and Molecular Design for Jiangsu Province, College of Animal Science and Technology, Yangzhou University, Yangzhou 225009, China.
Joint International Research Laboratory of Agriculture and Agri-Product Safety of the Ministry of Education of China, Yangzhou University, Yangzhou 225009, China.
Animals (Basel). 2020 Dec 28;11(1):43. doi: 10.3390/ani11010043.
and are two homologues of the same family of RNA binding proteins (RBPs). The function and molecular mechanism of in the formation of primordial germ cells (PGCs) are very clear, but the related research on is rarely reported. Here, we found that the overexpression of can promote the formation of PGC in vivo. Furthermore, the overexpression of also resulted in the inhibition of totipotency gene expression and upregulated the PGCs marker genes, and a significant increase in the number of PGCs in genital ridge, as detected by Periodic Acid-Schiff(PAS) staining. However, the inhibited expression showed completely opposite results, which were confirmed on the PGC induction model in vitro. Mechanistically, we found that the overexpression of can inhibit the maturation of , and the results of high-throughput sequencing indicated that was a negative regulator of the formation process of PGCs. Therefore, we conclude that our results determine that participates in the formation of PGCs through , which set a theoretical foundation for improving the function and mechanism of family in the formation of PGCs.
和是同一RNA结合蛋白(RBP)家族的两个同源物。在原始生殖细胞(PGC)形成中的功能和分子机制非常清楚,但关于的相关研究报道很少。在这里,我们发现的过表达可以促进体内PGC的形成。此外,的过表达还导致全能性基因表达受到抑制,PGC标记基因上调,并且通过高碘酸-希夫(PAS)染色检测到生殖嵴中PGC的数量显著增加。然而,抑制的表达显示出完全相反的结果,这在体外PGC诱导模型上得到了证实。从机制上讲,我们发现的过表达可以抑制的成熟,高通量测序结果表明是PGC形成过程的负调节因子。因此,我们得出结论,我们的结果确定通过参与PGC的形成,这为完善家族在PGC形成中的功能和机制奠定了理论基础。