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RCA 基因簇的调控结构捕获了基因内 TAD 边界、CTCF 介导的染色质环和长距离基因间增强子。

Regulatory Architecture of the RCA Gene Cluster Captures an Intragenic TAD Boundary, CTCF-Mediated Chromatin Looping and a Long-Range Intergenic Enhancer.

机构信息

School of Biomedical Sciences, The University of Western Australia, Crawley, WA, Australia.

Harry Perkins Institute of Medical Research, QEII Medical Centre, Nedlands, WA, Australia.

出版信息

Front Immunol. 2022 Jun 13;13:901747. doi: 10.3389/fimmu.2022.901747. eCollection 2022.

DOI:10.3389/fimmu.2022.901747
PMID:35769482
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9235356/
Abstract

The 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 (), 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 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 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 ( and ) 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.

摘要

补体激活调控因子(RCA)基因簇包含几个串联排列的基因,它们在免疫系统中具有共同的功能。RCA 成员,如补体受体 2(),是复杂自身免疫性疾病中公认的易感基因。已经在功能和遗传水平上证明了 RCA 基因的表达发生改变,但它们的调控机制尚未完全阐明。我们旨在研究 RCA 基因簇的结构组织,以确定影响该免疫调节区域中表达的关键调节元件和其他基因。使用 4C,我们在 B 细胞中捕获了 RCA 基因簇中广泛的 CTCF 介导的染色质环,表明这些环被组织成两个拓扑关联域(TAD)。有趣的是,一个 TAD 边界位于基因内一个特征性的片段重复区域。此外,我们在该区域绘制了许多基因-基因和基因-增强子相互作用,揭示了广泛的共调控。重要的是,我们鉴定了一个基因间增强子,并在 B 细胞中功能证明该元件上调了两个 RCA 成员(和)。我们揭示了新的、长程机制,自身免疫性疾病易感性可能受到遗传变异的影响,从而突出了染色质拓扑结构对基因调控和复杂遗传性疾病的重要贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4359/9235356/ad1601e7d6e7/fimmu-13-901747-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4359/9235356/c566b9915f88/fimmu-13-901747-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4359/9235356/7cf8855639bd/fimmu-13-901747-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4359/9235356/ca35ebf21625/fimmu-13-901747-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4359/9235356/694a940dd91a/fimmu-13-901747-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4359/9235356/6b7adb173a34/fimmu-13-901747-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4359/9235356/c5cac630c4f8/fimmu-13-901747-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4359/9235356/ad1601e7d6e7/fimmu-13-901747-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4359/9235356/c566b9915f88/fimmu-13-901747-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4359/9235356/7cf8855639bd/fimmu-13-901747-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4359/9235356/ca35ebf21625/fimmu-13-901747-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4359/9235356/694a940dd91a/fimmu-13-901747-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4359/9235356/6b7adb173a34/fimmu-13-901747-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4359/9235356/c5cac630c4f8/fimmu-13-901747-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4359/9235356/ad1601e7d6e7/fimmu-13-901747-g007.jpg

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