Mentch Samantha J, Locasale Jason W
Field of Biochemistry, Molecular, and Cell Biology, Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York.
Department of Pharmacology and Cancer Biology, Duke University School of Medicine, Durham, North Carolina.
Ann N Y Acad Sci. 2016 Jan;1363(1):91-8. doi: 10.1111/nyas.12956. Epub 2015 Dec 8.
One-carbon metabolism is a metabolic network that integrates nutrient status from the environment to yield multiple biological functions. The folate and methionine cycles generate S-adenosylmethionine (SAM), which is the universal methyl donor for methylation reactions, including histone and DNA methylation. Histone methylation is a crucial part of the epigenetic code and plays diverse roles in the establishment of chromatin states that mediate the regulation of gene expression. The activities of histone methyltransferases (HMTs) are dependent on intracellular levels of SAM, which fluctuate based on cellular nutrient availability, providing a link between cell metabolism and histone methylation. Here we discuss the biochemical properties of HMTs, their role in gene regulation, and the connection to cellular metabolism. Our emphasis is on understanding the specificity of this intriguing link.
一碳代谢是一个整合来自环境的营养状况以产生多种生物学功能的代谢网络。叶酸和甲硫氨酸循环产生S-腺苷甲硫氨酸(SAM),它是包括组蛋白和DNA甲基化在内的甲基化反应的通用甲基供体。组蛋白甲基化是表观遗传密码的关键部分,在介导基因表达调控的染色质状态建立中发挥多种作用。组蛋白甲基转移酶(HMTs)的活性取决于SAM的细胞内水平,SAM水平会根据细胞营养物质的可利用性而波动,这提供了细胞代谢与组蛋白甲基化之间的联系。在此,我们讨论HMTs的生化特性、它们在基因调控中的作用以及与细胞代谢的联系。我们的重点是理解这一有趣联系的特异性。