昼夜节律
肠易激综合征
染色质
糖皮质激素受体
生物
内分泌学
内科学
糖皮质激素
细胞生物学
医学
遗传学
基因
作者
Gen Zheng,Suya Pang,Junbao Wang,Fangyu Wang,Qi Wang,Lili Yang,Mengdie Ji,Dejian Xie,Shengtao Zhu,Chen Yang,Yan Zhou,Gerald A. Higgins,John Wiley,Xiaohua Hou,Rong Lin
出处
期刊:iScience
[Cell Press]
日期:2023-06-17
卷期号:26 (7): 107137-107137
被引量:15
标识
DOI:10.1016/j.isci.2023.107137
摘要
Stress-elevated glucocorticoids cause circadian disturbances and gut-brain axis (GBA) disorders, including irritable bowel syndrome (IBS). We hypothesized that the glucocorticoid receptor (GR/NR3C1) might cause chromatin circadian misalignment in the colon epithelium. We observed significantly decreased core circadian gene Nr1d1 in water avoidance stressed (WAS) BALB/c colon epithelium, like in IBS patients. WAS decreased GR binding at the Nr1d1 promoter E-box (enhancer box), and GR could suppress Nr1d1 via this site. Stress also altered GR binding at the E-box sites along the Ikzf3-Nr1d1 chromatin and remodeled circadian chromatin 3D structures, including Ikzf3-Nr1d1 super-enhancer, Dbp, and Npas2. Intestinal deletion of Nr3c1 specifically abolished these stress-induced transcriptional alternations relevant to IBS phenotypes in BALB/c mice. GR mediated Ikzf3-Nr1d1 chromatin disease related circadian misalignment in stress-induced IBS animal model. This animal model dataset suggests that regulatory SNPs of human IKZF3-NR1D1 transcription through conserved chromatin looping have translational potential based on the GR-mediated circadian-stress crosstalk.
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