The Association Between Vitamin D and Multiple Sclerosis Risk: 1,25(OH)2D3 Induces Super-Enhancers Bound by VDR

被引:25
作者
Lu, Ming [1 ,2 ]
McComish, Bennet J. [1 ]
Burdon, Kathryn P. [1 ]
Taylor, Bruce, V [1 ]
Korner, Heinrich [1 ,3 ]
机构
[1] Univ Tasmania, Menzies Inst Med Res, Hobart, Tas, Australia
[2] Anhui Med Univ, Dept Immunol, Hefei, Anhui, Peoples R China
[3] Anhui Med Univ, Inst Clin Pharmacol, Collaborat Innovat Ctr Antiinflammatory & Immune, Key Lab Antiinflammatory & Immunopharmacol,Minist, Hefei, Anhui, Peoples R China
关键词
vitamin D; vitamin D receptor; inducible super-enhancer; risk allele; multiple sclerosis; D-RECEPTOR BINDING; MOLECULAR PHENOTYPE; CELL IDENTITY; HUMAN MONOCYTES; MESSENGER-RNA; GENE; TRANSCRIPTION; EXPRESSION; INHIBITION; PACKAGE;
D O I
10.3389/fimmu.2019.00488
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A super-enhancer (SE) is a cluster of enhancers with a relatively high density of particular chromatin features. SEs typically regulate key genes that can determine cell identity and differentiation. Identifying SEs and their effects may be critical in predicting key regulatory genes, such as master transcription factor genes or oncogenes. Signal inducible SEs are dense stretches of signal terminal transcription factor (TF) binding regions, and may modulate the interaction between environmental factors (e.g., Vitamin D) and genetic factors (i.e., risk variants) in complex diseases such as multiple sclerosis (MS). As a complex autoimmune disease, the etiology and progression of MS, including the interaction between Vitamin D and MS risk variants, is still unclear and can be explored from the aspect of signal SEs. Vitamin D [with its active form: 1,25(OH)(2)D-3], is an environmental risk factor for MS. It binds the Vitamin D receptor (VDR) and regulates gene expression. This study explores the association between VDR super-enhancers (VSEs) and MS risk variants. Firstly, we reanalyse public ChIP-seq and RNA-seq data to classify VSEs into three categories according to their combinations of persistent and secondary VDR binding. Secondly, we indicate the genes with VSE regions that are near MS risk variants. Furthermore, we find that MS risk variants are enriched in VSE regions, and we indicate some genes with a VSE overlapping MS risk variant for further exploration. We also find two clusters of genes from the set of genes showing correlation of expression patterns with the MS risk gene ZMIZ1 that appear to be regulated by VSEs in THP-1 cells. It is the first time that VSEs have been analyzed, and we directly connect the genetic risk factors for MS risk with Vitamin D based on VSEs.
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页数:16
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