Reproductive Medicine Center, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Department of Obstetrics and Gynecology, Affiliated Dongguan People's Hospital, Southern Medical University, Dongguan, China.
Front Endocrinol (Lausanne). 2022 Jul 22;13:907286. doi: 10.3389/fendo.2022.907286. eCollection 2022.
maturation (IVM) refers to the process of developing immature oocytes into the mature under the microenvironment analogous to follicle fluid. It is an important technique for patients with polycystic ovary syndrome and, especially, those young patients with the need of fertility preservation. However, as the mechanisms of oocyte maturation have not been fully understood yet, the cultivation efficiency of IVM is not satisfactory. It was confirmed in our previous study that oocyte maturation was impaired after N-acetyltransferase 10 (NAT10) knockdown (KD). In the present study, we further explored the transcriptome alteration of NAT10-depleted oocytes and found that () was an important target gene for NAT10-mediated ac4C modification in oocyte maturation. NAT10 might regulate stability and expression by suppressing its degradation. To find out whether the influence of NAT10-mediated ac4C on oocyte maturation was mediated by , we further explored the role of in IVM. After knocking down OGA of oocytes, oocyte maturation was inhibited. In addition, as oocytes matured, expression increased and, conversely, O-linked N-acetylglucosamine (O-GlcNAc) level decreased. On the basis of NAT10 KD transcriptome and OGA KD transcriptome data, NAT10-mediated ac4C modification of might play a role through G protein-coupled receptors, molecular transduction, nucleosome DNA binding, and other mechanisms in oocyte maturation. , , , , , and were potential downstream genes. In conclusion, NAT10 maintained the stability of transcript by ac4C modification on it, thus positively regulating IVM. Moreover, our study revealed the regulation mechanisms of oocytes maturation and provided reference for improving IVM outcomes. At the same time, the interaction between mRNA ac4C modification and protein O-GlcNAc modification was found for the first time, which enriched the regulation network of oocyte maturation.
卵母细胞成熟(IVM)是指在类似于卵泡液的微环境中使未成熟卵母细胞发育成熟的过程。这是多囊卵巢综合征患者,尤其是需要生育力保存的年轻患者的一项重要技术。然而,由于卵母细胞成熟的机制尚未完全阐明,IVM 的培养效率并不令人满意。我们之前的研究证实,N-乙酰转移酶 10(NAT10)敲低(KD)后卵母细胞成熟受损。在本研究中,我们进一步探讨了 NAT10 耗尽的卵母细胞转录组变化,发现()是 NAT10 介导的卵母细胞成熟中 ac4C 修饰的重要靶基因。NAT10 可能通过抑制其降解来调节()的稳定性和表达。为了确定 NAT10 介导的 ac4C 对卵母细胞成熟的影响是否是通过()介导的,我们进一步探讨了()在 IVM 中的作用。敲低卵母细胞中的 OGA 后,卵母细胞成熟受到抑制。此外,随着卵母细胞成熟,()的表达增加,相反,O-连接的 N-乙酰葡萄糖胺(O-GlcNAc)水平降低。基于 NAT10 KD 转录组和 OGA KD 转录组数据,NAT10 介导的()ac4C 修饰可能通过 G 蛋白偶联受体、分子转导、核小体 DNA 结合等机制在卵母细胞成熟中发挥作用。()、()、()、()和()是潜在的下游基因。总之,NAT10 通过对其进行 ac4C 修饰来维持()转录本的稳定性,从而正向调节 IVM。此外,我们的研究揭示了卵母细胞成熟的调控机制,为改善 IVM 结果提供了参考。同时,首次发现了 mRNA ac4C 修饰与蛋白质 O-GlcNAc 修饰之间的相互作用,丰富了卵母细胞成熟的调控网络。