Basurto-Cayuela Laura, Guerrero-Martínez José A, Gómez-Marín Elena, Sánchez-Escabias Elena, Escaño-Maestre María, Ceballos-Chávez María, Reyes José C
Genome Biology Department, Centro Andaluz de Biología Molecular y Medicina Regenerativa-CABIMER, Consejo Superior de Investigaciones Científicas-Universidad de Sevilla-Universidad Pablo de Olavide (CSIC-USE-UPO), Av. Americo Vespucio, 41092 Seville, Spain.
Genome Biology Department, Centro Andaluz de Biología Molecular y Medicina Regenerativa-CABIMER, Consejo Superior de Investigaciones Científicas-Universidad de Sevilla-Universidad Pablo de Olavide (CSIC-USE-UPO), Av. Americo Vespucio, 41092 Seville, Spain.
Cell Rep. 2024 Mar 26;43(3):113855. doi: 10.1016/j.celrep.2024.113855. Epub 2024 Mar 1.
SWI/SNF complexes are evolutionarily conserved, ATP-dependent chromatin remodeling machines. Here, we characterize the features of SWI/SNF-dependent genes using BRM014, an inhibitor of the ATPase activity of the complexes. We find that SWI/SNF activity is required to maintain chromatin accessibility and nucleosome occupancy for most enhancers but not for most promoters. SWI/SNF activity is needed for expression of genes with low to medium levels of expression that have promoters with (1) low chromatin accessibility, (2) low levels of active histone marks, (3) high H3K4me1/H3K4me3 ratio, (4) low nucleosomal phasing, and (5) enrichment in TATA-box motifs. These promoters are mostly occupied by the canonical Brahma-related gene 1/Brahma-associated factor (BAF) complex. These genes are surrounded by SWI/SNF-dependent enhancers and mainly encode signal transduction, developmental, and cell identity genes (with almost no housekeeping genes). Machine-learning models trained with different chromatin characteristics of promoters and their surrounding regulatory regions indicate that the chromatin landscape is a determinant for establishing SWI/SNF dependency.
SWI/SNF复合物是进化上保守的、依赖ATP的染色质重塑机器。在此,我们使用BRM014(该复合物ATP酶活性的抑制剂)来表征SWI/SNF依赖性基因的特征。我们发现,对于大多数增强子而言,维持染色质可及性和核小体占据需要SWI/SNF活性,但对于大多数启动子则不然。对于表达水平低至中等、具有以下特征启动子的基因的表达,需要SWI/SNF活性:(1) 染色质可及性低;(2) 活性组蛋白标记水平低;(3) H3K4me1/H3K4me3比例高;(4) 核小体相位低;(5) TATA盒基序富集。这些启动子大多被经典的与婆罗门相关基因1/婆罗门相关因子(BAF)复合物占据。这些基因被SWI/SNF依赖性增强子包围,主要编码信号转导、发育和细胞身份基因(几乎没有管家基因)。用启动子及其周围调控区域的不同染色质特征训练的机器学习模型表明,染色质格局是建立SWI/SNF依赖性的一个决定因素。