表观遗传学
新陈代谢
生物合成
生物化学
甲基化
基因亚型
半胱氨酸
生物
组蛋白
化学
基因
酶
作者
Vanha N. Pham,Kevin J. Bruemmer,Joel D. W. Toh,Eva J. Ge,Logan Tenney,Carl C. Ward,Felix A. Dingler,Christopher L. Millington,Carlos A. García‐Prieto,Mia C. Pulos-Holmes,Nicholas T. Ingolia,Lucas B. Pontel,Manel Esteller,Ketan J. Patel,Daniel K. Nomura,Christopher J. Chang
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2023-11-02
卷期号:382 (6670)
被引量:18
标识
DOI:10.1126/science.abp9201
摘要
One-carbon metabolism is an essential branch of cellular metabolism that intersects with epigenetic regulation. In this work, we show how formaldehyde (FA), a one-carbon unit derived from both endogenous sources and environmental exposure, regulates one-carbon metabolism by inhibiting the biosynthesis of S -adenosylmethionine (SAM), the major methyl donor in cells. FA reacts with privileged, hyperreactive cysteine sites in the proteome, including Cys120 in S-adenosylmethionine synthase isoform type-1 (MAT1A). FA exposure inhibited MAT1A activity and decreased SAM production with MAT-isoform specificity. A genetic mouse model of chronic FA overload showed a decrease n SAM and in methylation on selected histones and genes. Epigenetic and transcriptional regulation of Mat1a and related genes function as compensatory mechanisms for FA-dependent SAM depletion, revealing a biochemical feedback cycle between FA and SAM one-carbon units.
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