{"title":"调控表观遗传学:甲基转移酶SETD6的综合综述。","authors":"Anand Chopra, Michal Feldman, Dan Levy","doi":"10.1038/s12276-025-01423-2","DOIUrl":null,"url":null,"abstract":"Transcription is regulated by an intricate and extensive network of regulatory factors that impinge upon target genes. This process involves crosstalk between a plethora of factors that include chromatin structure, transcription factors and posttranslational modifications (PTMs). Among PTMs, lysine methylation has emerged as a key transcription regulatory PTM that occurs on histone and non-histone proteins, and several enzymatic regulators of lysine methylation are attractive targets for disease intervention. SET domain-containing protein 6 (SETD6) is a mono-methyltransferase that promotes the methylation of multiple transcription factors and other proteins involved in the regulation of gene expression programs. Many of these SETD6 substrates, such as the canonical SETD6 substrate RELA, are linked to cellular pathways that are highly relevant to human health and disease. Furthermore, SETD6 regulates numerous cancerous phenotypes and guards cancer cells from apoptosis. In the past 15 years, our knowledge of SETD6 substrate methylation and the biological roles of this enzyme has grown immensely. Here we provide a comprehensive overview of SETD6 that will enhance our understanding of this enzyme’s role in chromatin and in selective transcriptional control, the contextual biological roles of this enzyme, and the molecular mechanisms and pathways in which SETD6 is involved, and we highlight the major trends in the SETD6 field. The chemical modification of proteins, such as lysine methylation, influences their role in the cell. This review focuses on an epigenetic enzyme called SETD6 that adds small chemical methyl groups to certain proteins. Over the past 15 years, research on SETD6 has shown that it plays an important role in human health and disease. The interactions of SETD6 with other proteins, particularly its ability to chemically modify them, have been shown to influence the individual functions of these proteins. This influence affects cells at the epigenetic level—affecting gene regulation—as well as cell behavior. Whether SETD6 promotes or suppresses cancerous properties depends on the type of cancer. Therefore, research focusing on the role of SETD6 in the cell is crucial to understand whether SETD6 could be a promising target for therapeutic intervention. .","PeriodicalId":50466,"journal":{"name":"Experimental and Molecular Medicine","volume":"57 3","pages":"533-544"},"PeriodicalIF":9.5000,"publicationDate":"2025-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.com/articles/s12276-025-01423-2.pdf","citationCount":"0","resultStr":"{\"title\":\"Orchestrating epigenetics: a comprehensive review of the methyltransferase SETD6\",\"authors\":\"Anand Chopra, Michal Feldman, Dan Levy\",\"doi\":\"10.1038/s12276-025-01423-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Transcription is regulated by an intricate and extensive network of regulatory factors that impinge upon target genes. This process involves crosstalk between a plethora of factors that include chromatin structure, transcription factors and posttranslational modifications (PTMs). Among PTMs, lysine methylation has emerged as a key transcription regulatory PTM that occurs on histone and non-histone proteins, and several enzymatic regulators of lysine methylation are attractive targets for disease intervention. SET domain-containing protein 6 (SETD6) is a mono-methyltransferase that promotes the methylation of multiple transcription factors and other proteins involved in the regulation of gene expression programs. Many of these SETD6 substrates, such as the canonical SETD6 substrate RELA, are linked to cellular pathways that are highly relevant to human health and disease. Furthermore, SETD6 regulates numerous cancerous phenotypes and guards cancer cells from apoptosis. In the past 15 years, our knowledge of SETD6 substrate methylation and the biological roles of this enzyme has grown immensely. Here we provide a comprehensive overview of SETD6 that will enhance our understanding of this enzyme’s role in chromatin and in selective transcriptional control, the contextual biological roles of this enzyme, and the molecular mechanisms and pathways in which SETD6 is involved, and we highlight the major trends in the SETD6 field. The chemical modification of proteins, such as lysine methylation, influences their role in the cell. This review focuses on an epigenetic enzyme called SETD6 that adds small chemical methyl groups to certain proteins. Over the past 15 years, research on SETD6 has shown that it plays an important role in human health and disease. The interactions of SETD6 with other proteins, particularly its ability to chemically modify them, have been shown to influence the individual functions of these proteins. This influence affects cells at the epigenetic level—affecting gene regulation—as well as cell behavior. Whether SETD6 promotes or suppresses cancerous properties depends on the type of cancer. Therefore, research focusing on the role of SETD6 in the cell is crucial to understand whether SETD6 could be a promising target for therapeutic intervention. .\",\"PeriodicalId\":50466,\"journal\":{\"name\":\"Experimental and Molecular Medicine\",\"volume\":\"57 3\",\"pages\":\"533-544\"},\"PeriodicalIF\":9.5000,\"publicationDate\":\"2025-03-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.nature.com/articles/s12276-025-01423-2.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Experimental and Molecular Medicine\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.nature.com/articles/s12276-025-01423-2\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Experimental and Molecular Medicine","FirstCategoryId":"3","ListUrlMain":"https://www.nature.com/articles/s12276-025-01423-2","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Orchestrating epigenetics: a comprehensive review of the methyltransferase SETD6
Transcription is regulated by an intricate and extensive network of regulatory factors that impinge upon target genes. This process involves crosstalk between a plethora of factors that include chromatin structure, transcription factors and posttranslational modifications (PTMs). Among PTMs, lysine methylation has emerged as a key transcription regulatory PTM that occurs on histone and non-histone proteins, and several enzymatic regulators of lysine methylation are attractive targets for disease intervention. SET domain-containing protein 6 (SETD6) is a mono-methyltransferase that promotes the methylation of multiple transcription factors and other proteins involved in the regulation of gene expression programs. Many of these SETD6 substrates, such as the canonical SETD6 substrate RELA, are linked to cellular pathways that are highly relevant to human health and disease. Furthermore, SETD6 regulates numerous cancerous phenotypes and guards cancer cells from apoptosis. In the past 15 years, our knowledge of SETD6 substrate methylation and the biological roles of this enzyme has grown immensely. Here we provide a comprehensive overview of SETD6 that will enhance our understanding of this enzyme’s role in chromatin and in selective transcriptional control, the contextual biological roles of this enzyme, and the molecular mechanisms and pathways in which SETD6 is involved, and we highlight the major trends in the SETD6 field. The chemical modification of proteins, such as lysine methylation, influences their role in the cell. This review focuses on an epigenetic enzyme called SETD6 that adds small chemical methyl groups to certain proteins. Over the past 15 years, research on SETD6 has shown that it plays an important role in human health and disease. The interactions of SETD6 with other proteins, particularly its ability to chemically modify them, have been shown to influence the individual functions of these proteins. This influence affects cells at the epigenetic level—affecting gene regulation—as well as cell behavior. Whether SETD6 promotes or suppresses cancerous properties depends on the type of cancer. Therefore, research focusing on the role of SETD6 in the cell is crucial to understand whether SETD6 could be a promising target for therapeutic intervention. .
期刊介绍:
Experimental & Molecular Medicine (EMM) stands as Korea's pioneering biochemistry journal, established in 1964 and rejuvenated in 1996 as an Open Access, fully peer-reviewed international journal. Dedicated to advancing translational research and showcasing recent breakthroughs in the biomedical realm, EMM invites submissions encompassing genetic, molecular, and cellular studies of human physiology and diseases. Emphasizing the correlation between experimental and translational research and enhanced clinical benefits, the journal actively encourages contributions employing specific molecular tools. Welcoming studies that bridge basic discoveries with clinical relevance, alongside articles demonstrating clear in vivo significance and novelty, Experimental & Molecular Medicine proudly serves as an open-access, online-only repository of cutting-edge medical research.