H3K18 lactylation marks tissue-specific active enhancers

生物 H3K4me3 增强子 表观遗传学 组蛋白 管家基因 基因 发起人 基因表达调控 遗传学 表观遗传学 基因表达 CpG站点 计算生物学 DNA甲基化
作者
Eva Galle,Chee-Wai Wong,Adhideb Ghosh,Thibaut Desgeorges,Kate Melrose,Laura C. Hinte,Daniel Castellano‐Castillo,Magdalena Engl,João Agostinho de Sousa,Francisco Javier Ruiz‐Ojeda,Katrien De Bock,Jonatan R. Ruiz,Ferdinand von Meyenn
出处
期刊:Genome Biology [BioMed Central]
卷期号:23 (1): 207-207 被引量:153
标识
DOI:10.1186/s13059-022-02775-y
摘要

Histone lactylation has been recently described as a novel histone post-translational modification linking cellular metabolism to epigenetic regulation.Given the expected relevance of this modification and current limited knowledge of its function, we generate genome-wide datasets of H3K18la distribution in various in vitro and in vivo samples, including mouse embryonic stem cells, macrophages, adipocytes, and mouse and human skeletal muscle. We compare them to profiles of well-established histone modifications and gene expression patterns. Supervised and unsupervised bioinformatics analysis shows that global H3K18la distribution resembles H3K27ac, although we also find notable differences. H3K18la marks active CpG island-containing promoters of highly expressed genes across most tissues assessed, including many housekeeping genes, and positively correlates with H3K27ac and H3K4me3 as well as with gene expression. In addition, H3K18la is enriched at active enhancers that lie in proximity to genes that are functionally important for the respective tissue.Overall, our data suggests that H3K18la is not only a marker for active promoters, but also a mark of tissue specific active enhancers.
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