生物
维甲酸
骨化三醇受体
趋同(经济学)
遗传学
信号转导
维生素
视黄醇X受体
维生素D与神经学
计算生物学
维甲酸
细胞生物学
基因
核受体
生物化学
转录因子
内分泌学
经济
经济增长
作者
Hamidreza Mianesaz,Lóránd Göczi,Gergely Nagy,Szilárd Póliska,Lina Fadel,Dóra Bojcsuk,András Penyige,Krisztina Szirák,Farah AlHaman,László Nagy,György Vámosi,Lajos Széles
出处
期刊:PubMed
日期:2025-03-20
卷期号:53 (6)
摘要
Retinoic acid receptors (RARs) and the vitamin D receptor (VDR) regulate distinct but overlapping gene sets in multiple cell types. The abundance and characteristics of regulatory regions, occupied by both RARs and VDR are largely unexplored. We used global approaches (ChIP-seq, RNA-seq, and ATAC-seq) and bioinformatics tools to map and characterize common binding regions of RARα and VDR in differentiated human THP-1 cells. We found that the cistromes of ligand-activated RARα and VDR largely overlapped, and their agonists (AM580 and calcitriol) co-regulated several genes, often cooperatively. Common binding regions were frequently (but not exclusively) annotated with co-regulated genes and exhibited increased MED1 occupancy upon ligand stimulation, suggesting their involvement in gene regulation. Chromatin accessibility was typically higher in the common regions than in regions occupied exclusively by RARα or VDR. DNA response elements for RARα (DR1/2/5) and VDR (DR3) were enriched in the common regions, albeit the co-occurrence of the two types of canonical motifs was low (8.4%), suggesting that "degenerate" DR1/2/5 and DR3 motifs or other sequences could mediate the binding. In summary, common binding regions of RARα and VDR are at the crossroads of the retinoid and vitamin D pathways, playing important roles in their convergence and cooperation.
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