Jiafeng Lu , Ming Zhang , Zhenxing Liu , Ling Guo , Peng Huang , Wenjuan Xia , Jincheng Li , Jinghuan Lv , Hoi-Hung Cheung , Chenyue Ding , Hong Li , Boxian Huang
{"title":"NSUN2-Mediated m5C Methylation Impairs Endometrial Receptivity","authors":"Jiafeng Lu , Ming Zhang , Zhenxing Liu , Ling Guo , Peng Huang , Wenjuan Xia , Jincheng Li , Jinghuan Lv , Hoi-Hung Cheung , Chenyue Ding , Hong Li , Boxian Huang","doi":"10.1016/j.labinv.2024.100327","DOIUrl":null,"url":null,"abstract":"<div><p>Impaired endometrial decidualization is the primary cause of recurrent implantation failure (RIF). RNA methylation modification, especially NSUN family mediated m<sup>5</sup>C, is crucial for various physiological events, such as maternal-to-zygotic transition, gametogenesis, embryonic development, organismal lifespan, and cell cycle. However, the regulatory mechanisms between NSUN family mediated m<sup>5</sup>C modification and RIF remain unknown. We acquired <em>NSUN2</em> expression data of 15 human endometrium samples at proliferative and secretory stages from reproductive cell atlas. The overall pattern of m<sup>5</sup>C sites and genes was elucidated through m<sup>5</sup>C-BS-seq, whereas the overall m<sup>5</sup>C levels in different groups were revealed by dot blot assay. BrdU and western blotting assays were carried out to evaluate the role of <em>NSUN2</em> in proliferation and autophagy. The effects of <em>NSUN</em><em>2</em>-mediated m<sup>5</sup>C modification on embryo attachment were evaluated by an in vitro model of a confluent monolayer of Ishikawa cells cocultured with BeWo spheroids, and its downstream targets were evaluated by real-time reverse-transcription PCR and western blotting in Ishikawa cells. The molecular mechanism for <em>NSUN2</em> regulating its downstream targets’ expression was determined by Cut&Tag and coimmunoprecipitation assays. <em>NSUN2</em> was increased in SOX9<sup>+</sup> cells and widespread in epithelial cell type at the proliferative stage by previous single-cell RNA sequencing data. NSUN2 overexpression (NSUN2<sup>OE</sup>) in the Ishikawa cell line elevated m<sup>5</sup>C levels and promoted cell proliferation and autophagy. NSUN2<sup>OE</sup> reduced attachment efficiency of BeWo cell spheres. Overexpressed NSUN2 was found to increase <em>STAT1</em> and <em>MMP14</em> mRNA expressions by inducing exon skipping. NSUN2 interacted with CLDN4 through m<sup>5</sup>C modification, and NSUN2<sup>OE</sup> or NSUN2 knockdown resulted in a similar variation tendency of CLDN4. Overexpression of NSUN2 increased <em>CLDN4</em> H3K9ac modification by downregulating SIRT4 expression at the protein level, leading to the upregulation of <em>CLDN4</em> mRNA expression. Our results uncovered a novel intricate regulatory mechanism between <em>NSUN2</em>-mediated m<sup>5</sup>C and RIF and suggested a potential new therapeutic strategy for RIF.</p></div>","PeriodicalId":17930,"journal":{"name":"Laboratory Investigation","volume":null,"pages":null},"PeriodicalIF":5.1000,"publicationDate":"2024-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Laboratory Investigation","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0023683724000059","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0
Abstract
Impaired endometrial decidualization is the primary cause of recurrent implantation failure (RIF). RNA methylation modification, especially NSUN family mediated m5C, is crucial for various physiological events, such as maternal-to-zygotic transition, gametogenesis, embryonic development, organismal lifespan, and cell cycle. However, the regulatory mechanisms between NSUN family mediated m5C modification and RIF remain unknown. We acquired NSUN2 expression data of 15 human endometrium samples at proliferative and secretory stages from reproductive cell atlas. The overall pattern of m5C sites and genes was elucidated through m5C-BS-seq, whereas the overall m5C levels in different groups were revealed by dot blot assay. BrdU and western blotting assays were carried out to evaluate the role of NSUN2 in proliferation and autophagy. The effects of NSUN2-mediated m5C modification on embryo attachment were evaluated by an in vitro model of a confluent monolayer of Ishikawa cells cocultured with BeWo spheroids, and its downstream targets were evaluated by real-time reverse-transcription PCR and western blotting in Ishikawa cells. The molecular mechanism for NSUN2 regulating its downstream targets’ expression was determined by Cut&Tag and coimmunoprecipitation assays. NSUN2 was increased in SOX9+ cells and widespread in epithelial cell type at the proliferative stage by previous single-cell RNA sequencing data. NSUN2 overexpression (NSUN2OE) in the Ishikawa cell line elevated m5C levels and promoted cell proliferation and autophagy. NSUN2OE reduced attachment efficiency of BeWo cell spheres. Overexpressed NSUN2 was found to increase STAT1 and MMP14 mRNA expressions by inducing exon skipping. NSUN2 interacted with CLDN4 through m5C modification, and NSUN2OE or NSUN2 knockdown resulted in a similar variation tendency of CLDN4. Overexpression of NSUN2 increased CLDN4 H3K9ac modification by downregulating SIRT4 expression at the protein level, leading to the upregulation of CLDN4 mRNA expression. Our results uncovered a novel intricate regulatory mechanism between NSUN2-mediated m5C and RIF and suggested a potential new therapeutic strategy for RIF.
期刊介绍:
Laboratory Investigation is an international journal owned by the United States and Canadian Academy of Pathology. Laboratory Investigation offers prompt publication of high-quality original research in all biomedical disciplines relating to the understanding of human disease and the application of new methods to the diagnosis of disease. Both human and experimental studies are welcome.