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...

Full description

Bibliographic Details
Published in:Frontiers in Endocrinology
Main Authors: Jiayu Lin, Yuting Xiang, Jiana Huang, Haitao Zeng, Yanyan Zeng, Jiawen Liu, Taibao Wu, Qiqi Liang, Xiaoyan Liang, Jingjie Li, Chuanchuan Zhou
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-07-01
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2022.907286/full
_version_ 1852658914276933632
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
work_keys_str_mv AT jiayulin nat10maintainsogamrnastabilitythroughac4cmodificationinregulatingoocytematuration
AT yutingxiang nat10maintainsogamrnastabilitythroughac4cmodificationinregulatingoocytematuration
AT yutingxiang nat10maintainsogamrnastabilitythroughac4cmodificationinregulatingoocytematuration
AT jianahuang nat10maintainsogamrnastabilitythroughac4cmodificationinregulatingoocytematuration
AT haitaozeng nat10maintainsogamrnastabilitythroughac4cmodificationinregulatingoocytematuration
AT yanyanzeng nat10maintainsogamrnastabilitythroughac4cmodificationinregulatingoocytematuration
AT jiawenliu nat10maintainsogamrnastabilitythroughac4cmodificationinregulatingoocytematuration
AT taibaowu nat10maintainsogamrnastabilitythroughac4cmodificationinregulatingoocytematuration
AT qiqiliang nat10maintainsogamrnastabilitythroughac4cmodificationinregulatingoocytematuration
AT xiaoyanliang nat10maintainsogamrnastabilitythroughac4cmodificationinregulatingoocytematuration
AT jingjieli nat10maintainsogamrnastabilitythroughac4cmodificationinregulatingoocytematuration
AT chuanchuanzhou nat10maintainsogamrnastabilitythroughac4cmodificationinregulatingoocytematuration