{"title":"多重SNaPshot法分析唾液中性别特异性DNA甲基化差异","authors":"Priyanka Govender , Meenu Ghai , Farzeen Kader , Moses Okpeku , Marvellous Zhou","doi":"10.1016/j.genrep.2025.102268","DOIUrl":null,"url":null,"abstract":"<div><div>DNA methylation (DNAm) analysis is emerging as a sensitive method for studying sex-specific differences in humans. Methylation SNaPshot (mSNaPshot) is a robust technique which allows rapid quantification of site-specific DNAm levels and can multiplex several markers in a single reaction. Sex-specific DNAm differences have been observed in blood, placental and brain tissue, but it is not well studied in saliva and African populations. Therefore, this study was undertaken to multiplex three saliva-specific CpG sites in a mSNaPshot assay to analyze sex-specific differences in DNAm patterns of 100 healthy Sub-Saharan Africans. Three saliva-specific CpG sites located in genes, <em>FAM43A</em> (cg09652652-55d), <em>BCA</em>S<em>4</em> (Chr20: 4844305) and <em>FNDC1</em> (cg09107912) were selected for the multiplex assay. These markers were referred to as SAL-1 (<em>FAM43A</em>), SAL-2 (<em>BCAS4</em>) and SAL-3 (<em>FNDC1</em>). SAL-1 and SAL-3 displayed hypermethylation and hypomethylation, respectively in saliva. However, SAL-2 showed an unmethylation signal. Overall, males displayed higher average methylation (50.07 %) than females (42.39 %) for all three markers. Significant sex-specific DNAm differences were observed for SAL-1 and SAL-3 (<em>p</em> < 0.0001). Age did not affect DNAm at the three target sites. Our results indicated that sex-specific DNAm differences exist in body fluids, and SAL-1 and SAL-3 could assist in sex identification of a saliva sample by mSNaPshot assay. DNAm varies in different populations; hence, future studies should target diverse populations from different geographical locations to ascertain the specificity of the findings. We also highlight that sex-specific differential methylation holds great potential for identifying sex-specific biomarkers, improving diagnostics, early disease detection and monitoring, and development of target therapeutics.</div></div>","PeriodicalId":12673,"journal":{"name":"Gene Reports","volume":"40 ","pages":"Article 102268"},"PeriodicalIF":0.9000,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Analysis of sex-specific DNA methylation differences in saliva by multiplex SNaPshot assay\",\"authors\":\"Priyanka Govender , Meenu Ghai , Farzeen Kader , Moses Okpeku , Marvellous Zhou\",\"doi\":\"10.1016/j.genrep.2025.102268\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>DNA methylation (DNAm) analysis is emerging as a sensitive method for studying sex-specific differences in humans. Methylation SNaPshot (mSNaPshot) is a robust technique which allows rapid quantification of site-specific DNAm levels and can multiplex several markers in a single reaction. Sex-specific DNAm differences have been observed in blood, placental and brain tissue, but it is not well studied in saliva and African populations. Therefore, this study was undertaken to multiplex three saliva-specific CpG sites in a mSNaPshot assay to analyze sex-specific differences in DNAm patterns of 100 healthy Sub-Saharan Africans. Three saliva-specific CpG sites located in genes, <em>FAM43A</em> (cg09652652-55d), <em>BCA</em>S<em>4</em> (Chr20: 4844305) and <em>FNDC1</em> (cg09107912) were selected for the multiplex assay. These markers were referred to as SAL-1 (<em>FAM43A</em>), SAL-2 (<em>BCAS4</em>) and SAL-3 (<em>FNDC1</em>). SAL-1 and SAL-3 displayed hypermethylation and hypomethylation, respectively in saliva. However, SAL-2 showed an unmethylation signal. Overall, males displayed higher average methylation (50.07 %) than females (42.39 %) for all three markers. Significant sex-specific DNAm differences were observed for SAL-1 and SAL-3 (<em>p</em> < 0.0001). Age did not affect DNAm at the three target sites. Our results indicated that sex-specific DNAm differences exist in body fluids, and SAL-1 and SAL-3 could assist in sex identification of a saliva sample by mSNaPshot assay. DNAm varies in different populations; hence, future studies should target diverse populations from different geographical locations to ascertain the specificity of the findings. We also highlight that sex-specific differential methylation holds great potential for identifying sex-specific biomarkers, improving diagnostics, early disease detection and monitoring, and development of target therapeutics.</div></div>\",\"PeriodicalId\":12673,\"journal\":{\"name\":\"Gene Reports\",\"volume\":\"40 \",\"pages\":\"Article 102268\"},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2025-05-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Gene Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2452014425001414\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gene Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2452014425001414","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
Analysis of sex-specific DNA methylation differences in saliva by multiplex SNaPshot assay
DNA methylation (DNAm) analysis is emerging as a sensitive method for studying sex-specific differences in humans. Methylation SNaPshot (mSNaPshot) is a robust technique which allows rapid quantification of site-specific DNAm levels and can multiplex several markers in a single reaction. Sex-specific DNAm differences have been observed in blood, placental and brain tissue, but it is not well studied in saliva and African populations. Therefore, this study was undertaken to multiplex three saliva-specific CpG sites in a mSNaPshot assay to analyze sex-specific differences in DNAm patterns of 100 healthy Sub-Saharan Africans. Three saliva-specific CpG sites located in genes, FAM43A (cg09652652-55d), BCAS4 (Chr20: 4844305) and FNDC1 (cg09107912) were selected for the multiplex assay. These markers were referred to as SAL-1 (FAM43A), SAL-2 (BCAS4) and SAL-3 (FNDC1). SAL-1 and SAL-3 displayed hypermethylation and hypomethylation, respectively in saliva. However, SAL-2 showed an unmethylation signal. Overall, males displayed higher average methylation (50.07 %) than females (42.39 %) for all three markers. Significant sex-specific DNAm differences were observed for SAL-1 and SAL-3 (p < 0.0001). Age did not affect DNAm at the three target sites. Our results indicated that sex-specific DNAm differences exist in body fluids, and SAL-1 and SAL-3 could assist in sex identification of a saliva sample by mSNaPshot assay. DNAm varies in different populations; hence, future studies should target diverse populations from different geographical locations to ascertain the specificity of the findings. We also highlight that sex-specific differential methylation holds great potential for identifying sex-specific biomarkers, improving diagnostics, early disease detection and monitoring, and development of target therapeutics.
Gene ReportsBiochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.30
自引率
7.70%
发文量
246
审稿时长
49 days
期刊介绍:
Gene Reports publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses. Gene Reports strives to be a very diverse journal and topics in all fields will be considered for publication. Although not limited to the following, some general topics include: DNA Organization, Replication & Evolution -Focus on genomic DNA (chromosomal organization, comparative genomics, DNA replication, DNA repair, mobile DNA, mitochondrial DNA, chloroplast DNA). Expression & Function - Focus on functional RNAs (microRNAs, tRNAs, rRNAs, mRNA splicing, alternative polyadenylation) Regulation - Focus on processes that mediate gene-read out (epigenetics, chromatin, histone code, transcription, translation, protein degradation). Cell Signaling - Focus on mechanisms that control information flow into the nucleus to control gene expression (kinase and phosphatase pathways controlled by extra-cellular ligands, Wnt, Notch, TGFbeta/BMPs, FGFs, IGFs etc.) Profiling of gene expression and genetic variation - Focus on high throughput approaches (e.g., DeepSeq, ChIP-Seq, Affymetrix microarrays, proteomics) that define gene regulatory circuitry, molecular pathways and protein/protein networks. Genetics - Focus on development in model organisms (e.g., mouse, frog, fruit fly, worm), human genetic variation, population genetics, as well as agricultural and veterinary genetics. Molecular Pathology & Regenerative Medicine - Focus on the deregulation of molecular processes in human diseases and mechanisms supporting regeneration of tissues through pluripotent or multipotent stem cells.