Nshanian Michael, Geller Benjamin S, Gruber Joshua J, Chleilat Faye, Camarillo Jeannie Marie, Kelleher Neil L, Zhao Yingming, Snyder Michael P
Department of Genetics, Stanford University, School of Medicine, Stanford, CA.
Department of Chemistry, Molecular Biosciences and Proteomics Center of Excellence, Northwestern University, Evanston, IL.
Res Sq. 2024 Feb 16:rs.3.rs-3935562. doi: 10.21203/rs.3.rs-3935562/v1.
The short-chain fatty acids (SCFA) propionate and butyrate are produced in large amounts by microbial metabolism and have been identified as unique acyl lysine histone marks. In order to better understand the function of these modifications we used ChIP-seq to map the genome-wide location of four short-chain acyl histone marks H3K18pr/bu and H4K12pr/bu in treated and untreated colorectal cancer (CRC) and normal cells, as well as in mouse intestines . We correlate these marks with open chromatin regions along with gene expression to access the function of the target regions. Our data demonstrate that propionate and butyrate act as promoters of growth, differentiation as well as ion transport. We propose a mechanism involving direct modification of specific genomic regions, resulting in increased chromatin accessibility, and in case of butyrate, opposing effects on the proliferation of normal versus CRC cells.
短链脂肪酸(SCFA)丙酸酯和丁酸酯由微生物代谢大量产生,并已被鉴定为独特的酰基赖氨酸组蛋白标记。为了更好地理解这些修饰的功能,我们使用染色质免疫沉淀测序(ChIP-seq)来绘制四种短链酰基组蛋白标记H3K18pr/bu和H4K12pr/bu在经处理和未经处理的结直肠癌(CRC)及正常细胞以及小鼠肠道中的全基因组定位。我们将这些标记与开放染色质区域以及基因表达相关联,以了解靶区域的功能。我们的数据表明,丙酸酯和丁酸酯可作为生长、分化以及离子转运的促进剂。我们提出了一种机制,涉及特定基因组区域的直接修饰,导致染色质可及性增加,并且就丁酸酯而言,对正常细胞与CRC细胞的增殖具有相反的影响。