Department of Physiology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan.
Sci Rep. 2022 Dec 31;12(1):22648. doi: 10.1038/s41598-022-27293-6.
A mutation in the chromatin remodeler chromodomain helicase DNA-binding 7 (CHD7) gene causes the multiple congenital anomaly CHARGE syndrome. The craniofacial anomalies observed in CHARGE syndrome are caused by dysfunctions of neural crest cells (NCCs), which originate from the neural tube. However, the mechanism by which CHD7 regulates the function of human NCCs (hNCCs) remains unclear. We aimed to characterize the cis-regulatory elements governed by CHD7 in hNCCs by analyzing genome-wide ChIP-Seq data and identifying hNCC-specific CHD7-binding profiles. We compared CHD7-binding regions among cell types, including human induced pluripotent stem cells and human neuroepithelial cells, to determine the comprehensive properties of CHD7-binding in hNCCs. Importantly, analysis of the hNCC-specific CHD7-bound region revealed transcription factor AP-2α as a potential co-factor facilitating the cell type-specific transcriptional program in hNCCs. CHD7 was strongly associated with active enhancer regions, permitting the expression of hNCC-specific genes to sustain the function of hNCCs. Our findings reveal the regulatory mechanisms of CHD7 in hNCCs, thus providing additional information regarding the transcriptional programs in hNCCs.
染色质重塑因子 chromodomain 螺旋酶 DNA 结合蛋白 7 (CHD7) 基因突变导致多种先天性异常 CHARGE 综合征。CHARGE 综合征中观察到的颅面异常是由起源于神经管的神经嵴细胞 (NCC) 功能障碍引起的。然而,CHD7 调节人 NCCs (hNCCs) 功能的机制尚不清楚。我们旨在通过分析全基因组 ChIP-Seq 数据并鉴定 hNCC 特异性 CHD7 结合谱,来描述 CHD7 在 hNCCs 中调控的顺式调控元件。我们比较了包括人诱导多能干细胞和人神经上皮细胞在内的细胞类型中的 CHD7 结合区域,以确定 CHD7 在 hNCCs 中的综合结合特性。重要的是,对 hNCC 特异性 CHD7 结合区域的分析揭示了转录因子 AP-2α 作为一种潜在的辅助因子,有助于 hNCCs 中细胞类型特异性转录程序的表达。CHD7 与活性增强子区域强烈相关,允许 hNCC 特异性基因的表达,以维持 hNCC 的功能。我们的研究结果揭示了 CHD7 在 hNCCs 中的调控机制,从而为 hNCCs 中的转录程序提供了更多信息。