NAT10 Maintains OGA mRNA Stability Through ac4C Modification in Regulating Oocyte Maturation
In vitro maturation (IVM) refers to the process of developing immature oocytes into the mature in vitro 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 pr...
| Published in: | Frontiers in Endocrinology |
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| Main Authors: | , , , , , , , , , , |
| Format: | Article |
| Language: | English |
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Frontiers Media S.A.
2022-07-01
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| Online Access: | https://www.frontiersin.org/articles/10.3389/fendo.2022.907286/full |
| _version_ | 1852658914276933632 |
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| author | Jiayu Lin Yuting Xiang Yuting Xiang Jiana Huang Haitao Zeng Yanyan Zeng Jiawen Liu Taibao Wu Qiqi Liang Xiaoyan Liang Jingjie Li Chuanchuan Zhou |
| author_facet | Jiayu Lin Yuting Xiang Yuting Xiang Jiana Huang Haitao Zeng Yanyan Zeng Jiawen Liu Taibao Wu Qiqi Liang Xiaoyan Liang Jingjie Li Chuanchuan Zhou |
| author_sort | Jiayu Lin |
| collection | DOAJ |
| container_title | Frontiers in Endocrinology |
| description | In vitro maturation (IVM) refers to the process of developing immature oocytes into the mature in vitro 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 O-GlcNAcase(OGA) was an important target gene for NAT10-mediated ac4C modification in oocyte maturation. NAT10 might regulate OGA stability and expression by suppressing its degradation. To find out whether the influence of NAT10-mediated ac4C on oocyte maturation was mediated by OGA, we further explored the role of OGA in IVM. After knocking down OGA of oocytes, oocyte maturation was inhibited. In addition, as oocytes matured, OGA 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 OGA might play a role through G protein–coupled receptors, molecular transduction, nucleosome DNA binding, and other mechanisms in oocyte maturation. Rsph6a, Gm7788, Gm41780, Trpc7, Gm29036, and Gm47144 were potential downstream genes. In conclusion, NAT10 maintained the stability of OGA 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. |
| format | Article |
| id | doaj-art-cf7ba80ccb0a4121943aef059ff84d41 |
| institution | Directory of Open Access Journals |
| issn | 1664-2392 |
| language | English |
| publishDate | 2022-07-01 |
| publisher | Frontiers Media S.A. |
| record_format | Article |
| spelling | doaj-art-cf7ba80ccb0a4121943aef059ff84d412025-08-19T21:37:36ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922022-07-011310.3389/fendo.2022.907286907286NAT10 Maintains OGA mRNA Stability Through ac4C Modification in Regulating Oocyte MaturationJiayu Lin0Yuting Xiang1Yuting Xiang2Jiana Huang3Haitao Zeng4Yanyan Zeng5Jiawen Liu6Taibao Wu7Qiqi Liang8Xiaoyan Liang9Jingjie Li10Chuanchuan Zhou11Reproductive Medicine Center, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, ChinaReproductive Medicine Center, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, ChinaDepartment of Obstetrics and Gynecology, Affiliated Dongguan People’s Hospital, Southern Medical University, Dongguan, ChinaReproductive Medicine Center, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, ChinaReproductive Medicine Center, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, ChinaReproductive Medicine Center, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, ChinaReproductive Medicine Center, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, ChinaReproductive Medicine Center, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, ChinaReproductive Medicine Center, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, ChinaReproductive Medicine Center, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, ChinaReproductive Medicine Center, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, ChinaReproductive Medicine Center, Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, ChinaIn vitro maturation (IVM) refers to the process of developing immature oocytes into the mature in vitro 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 O-GlcNAcase(OGA) was an important target gene for NAT10-mediated ac4C modification in oocyte maturation. NAT10 might regulate OGA stability and expression by suppressing its degradation. To find out whether the influence of NAT10-mediated ac4C on oocyte maturation was mediated by OGA, we further explored the role of OGA in IVM. After knocking down OGA of oocytes, oocyte maturation was inhibited. In addition, as oocytes matured, OGA 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 OGA might play a role through G protein–coupled receptors, molecular transduction, nucleosome DNA binding, and other mechanisms in oocyte maturation. Rsph6a, Gm7788, Gm41780, Trpc7, Gm29036, and Gm47144 were potential downstream genes. In conclusion, NAT10 maintained the stability of OGA 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.https://www.frontiersin.org/articles/10.3389/fendo.2022.907286/fulloocytein vitro maturationNAT10N4-acetylcytidineOGAO-GlcNAc |
| spellingShingle | Jiayu Lin Yuting Xiang Yuting Xiang Jiana Huang Haitao Zeng Yanyan Zeng Jiawen Liu Taibao Wu Qiqi Liang Xiaoyan Liang Jingjie Li Chuanchuan Zhou NAT10 Maintains OGA mRNA Stability Through ac4C Modification in Regulating Oocyte Maturation oocyte in vitro maturation NAT10 N4-acetylcytidine OGA O-GlcNAc |
| title | NAT10 Maintains OGA mRNA Stability Through ac4C Modification in Regulating Oocyte Maturation |
| title_full | NAT10 Maintains OGA mRNA Stability Through ac4C Modification in Regulating Oocyte Maturation |
| title_fullStr | NAT10 Maintains OGA mRNA Stability Through ac4C Modification in Regulating Oocyte Maturation |
| title_full_unstemmed | NAT10 Maintains OGA mRNA Stability Through ac4C Modification in Regulating Oocyte Maturation |
| title_short | NAT10 Maintains OGA mRNA Stability Through ac4C Modification in Regulating Oocyte Maturation |
| title_sort | nat10 maintains oga mrna stability through ac4c modification in regulating oocyte maturation |
| topic | oocyte in vitro maturation NAT10 N4-acetylcytidine OGA O-GlcNAc |
| url | https://www.frontiersin.org/articles/10.3389/fendo.2022.907286/full |
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