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Título

Regulatory architecture of the RCA gene cluster captures an intragenic TAD boundary, CTCF-Mediated chromatin looping and a long-range intergenic enhancer

AutorCheng, Jessica; Clayton, Joshua S.; Acemel, Rafael D. CSIC ORCID; Zheng, Ye; Taylor, Rhonda L.; Keleş, Sündüz; Franke, Martin CSIC ORCID; Boackle, Susan A.; Harley, John B.; Quail, Elizabeth; Gómez-Skarmeta, José Luis CSIC ORCID ; Ulgiati, Daniela
Palabras claveRCA
B cells
Enhancers
Chromatin looping
TADs
Fecha de publicaciónjun-2022
EditorFrontiers Media
CitaciónFrontiers in Immunology 13: 901747 (2022)
ResumenThe Regulators of Complement Activation (RCA) gene cluster comprises several tandemly arranged genes with shared functions within the immune system. RCA members, such as complement receptor 2 (CR2), are well-established susceptibility genes in complex autoimmune diseases. Altered expression of RCA genes has been demonstrated at both the functional and genetic level, but the mechanisms underlying their regulation are not fully characterised. We aimed to investigate the structural organisation of the RCA gene cluster to identify key regulatory elements that influence the expression of CR2 and other genes in this immunomodulatory region. Using 4C, we captured extensive CTCF-mediated chromatin looping across the RCA gene cluster in B cells and showed these were organised into two topologically associated domains (TADs). Interestingly, an inter-TAD boundary was located within the CR1 gene at a well-characterised segmental duplication. Additionally, we mapped numerous gene-gene and gene-enhancer interactions across the region, revealing extensive co-regulation. Importantly, we identified an intergenic enhancer and functionally demonstrated this element upregulates two RCA members (CR2 and CD55) in B cells. We have uncovered novel, long-range mechanisms whereby autoimmune disease susceptibility may be influenced by genetic variants, thus highlighting the important contribution of chromatin topology to gene regulation and complex genetic disease.
Versión del editorhttp://dx.doi.org/10.3389/fimmu.2022.901747
URIhttp://hdl.handle.net/10261/281465
DOI10.3389/fimmu.2022.901747
Identificadoresdoi: 10.3389/fimmu.2022.901747
e-issn: 1664-3224
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