{"title":"烟酰胺通过促进狼疮小鼠n4乙酰化修饰提高卵母细胞数量和质量","authors":"Yun Xie, Chuanchuan Zhou, Qi Guo, Yingchun Guo, Jiayi Guo, Lina Chen, Xiaoping Liu, Yanyan Zeng, Qiqi Liang, Taibao Wu, Jiawen Liu, Xiaoyan Liang","doi":"10.1126/sciadv.adu0955","DOIUrl":null,"url":null,"abstract":"<div >Patients with systemic lupus erythematosus (SLE) often have decreased fertility. Gene translation is crucial to oocyte meiosis and development. However, it remains unclear how SLE affects this process. Here, we used single-cell transcriptome and translatome sequencing to uncover a notable disruption in protein translation in oocytes from SLE mice, associated with the <i>N</i><sup>4</sup>-acetylcytidine (ac<sup>4</sup>C) modification. Inhibition of ac<sup>4</sup>C levels in vitro substantially reduced oocyte translation efficiency. Notably, through trace-cell ac<sup>4</sup>C-RNA immunoprecipitation (acRIP) sequencing, we mapped the ac<sup>4</sup>C landscape in SLE mouse oocytes and found that deficient ac<sup>4</sup>C modification substantially impaired the translation of <i>Zygote arrest 1</i>. Furthermore, we demonstrated that nicotinamide treatment notably and safely improved the quantity and quality of oocytes in SLE mice by enhancing ac<sup>4</sup>C modification levels. Our findings highlight the essential role of <i>N</i>- acetyltransferase 10 (NAT10)-mediated ac<sup>4</sup>C modification in abnormal oocyte development in SLE and suggest that nicotinamide holds promise for improving fertility in patients with SLE.</div>","PeriodicalId":21609,"journal":{"name":"Science Advances","volume":"11 29","pages":""},"PeriodicalIF":12.5000,"publicationDate":"2025-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.science.org/doi/reader/10.1126/sciadv.adu0955","citationCount":"0","resultStr":"{\"title\":\"Nicotinamide boosts oocyte quantity and quality by promoting N4-acetylation modification in lupus mice\",\"authors\":\"Yun Xie, Chuanchuan Zhou, Qi Guo, Yingchun Guo, Jiayi Guo, Lina Chen, Xiaoping Liu, Yanyan Zeng, Qiqi Liang, Taibao Wu, Jiawen Liu, Xiaoyan Liang\",\"doi\":\"10.1126/sciadv.adu0955\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div >Patients with systemic lupus erythematosus (SLE) often have decreased fertility. Gene translation is crucial to oocyte meiosis and development. However, it remains unclear how SLE affects this process. Here, we used single-cell transcriptome and translatome sequencing to uncover a notable disruption in protein translation in oocytes from SLE mice, associated with the <i>N</i><sup>4</sup>-acetylcytidine (ac<sup>4</sup>C) modification. Inhibition of ac<sup>4</sup>C levels in vitro substantially reduced oocyte translation efficiency. Notably, through trace-cell ac<sup>4</sup>C-RNA immunoprecipitation (acRIP) sequencing, we mapped the ac<sup>4</sup>C landscape in SLE mouse oocytes and found that deficient ac<sup>4</sup>C modification substantially impaired the translation of <i>Zygote arrest 1</i>. Furthermore, we demonstrated that nicotinamide treatment notably and safely improved the quantity and quality of oocytes in SLE mice by enhancing ac<sup>4</sup>C modification levels. Our findings highlight the essential role of <i>N</i>- acetyltransferase 10 (NAT10)-mediated ac<sup>4</sup>C modification in abnormal oocyte development in SLE and suggest that nicotinamide holds promise for improving fertility in patients with SLE.</div>\",\"PeriodicalId\":21609,\"journal\":{\"name\":\"Science Advances\",\"volume\":\"11 29\",\"pages\":\"\"},\"PeriodicalIF\":12.5000,\"publicationDate\":\"2025-07-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.science.org/doi/reader/10.1126/sciadv.adu0955\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Science Advances\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://www.science.org/doi/10.1126/sciadv.adu0955\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science Advances","FirstCategoryId":"103","ListUrlMain":"https://www.science.org/doi/10.1126/sciadv.adu0955","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
Nicotinamide boosts oocyte quantity and quality by promoting N4-acetylation modification in lupus mice
Patients with systemic lupus erythematosus (SLE) often have decreased fertility. Gene translation is crucial to oocyte meiosis and development. However, it remains unclear how SLE affects this process. Here, we used single-cell transcriptome and translatome sequencing to uncover a notable disruption in protein translation in oocytes from SLE mice, associated with the N4-acetylcytidine (ac4C) modification. Inhibition of ac4C levels in vitro substantially reduced oocyte translation efficiency. Notably, through trace-cell ac4C-RNA immunoprecipitation (acRIP) sequencing, we mapped the ac4C landscape in SLE mouse oocytes and found that deficient ac4C modification substantially impaired the translation of Zygote arrest 1. Furthermore, we demonstrated that nicotinamide treatment notably and safely improved the quantity and quality of oocytes in SLE mice by enhancing ac4C modification levels. Our findings highlight the essential role of N- acetyltransferase 10 (NAT10)-mediated ac4C modification in abnormal oocyte development in SLE and suggest that nicotinamide holds promise for improving fertility in patients with SLE.
期刊介绍:
Science Advances, an open-access journal by AAAS, publishes impactful research in diverse scientific areas. It aims for fair, fast, and expert peer review, providing freely accessible research to readers. Led by distinguished scientists, the journal supports AAAS's mission by extending Science magazine's capacity to identify and promote significant advances. Evolving digital publishing technologies play a crucial role in advancing AAAS's global mission for science communication and benefitting humankind.