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用于研究强直性脊柱炎三维基因组结构的染色体构象捕获方法。

Chromosome conformation capture approaches to investigate 3D genome architecture in Ankylosing Spondylitis.

作者信息

Davidson Connor, Wordsworth B Paul, Cohen Carla J, Knight Julian C, Vecellio Matteo

机构信息

Wellcome Centre of Human Genetics, University of Oxford, Oxford, United Kingdom.

Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, University of Oxford, Oxford, United Kingdom.

出版信息

Front Genet. 2023 Jan 25;14:1129207. doi: 10.3389/fgene.2023.1129207. eCollection 2023.

Abstract

Ankylosing Spondylitis (AS) is a chronic inflammatory arthritis of the spine exhibiting a strong genetic background. The mechanistic and functional understanding of the AS-associated genomic loci, identified with Genome Wide Association Studies (GWAS), remains challenging. Chromosome conformation capture (3C) and derivatives are recent techniques which are of great help in elucidating the spatial genome organization and of enormous support in uncover a mechanistic explanation for disease-associated genetic variants. The perturbation of three-dimensional (3D) genome hierarchy may lead to a plethora of human diseases, including rheumatological disorders. Here we illustrate the latest approaches and related findings on the field of genome organization, highlighting how the instability of 3D genome conformation may be among the causes of rheumatological disease phenotypes. We suggest a new perspective on the inclusive potential of a 3C approach to inform GWAS results in rheumatic diseases. 3D genome organization may ultimately lead to a more precise and comprehensive functional interpretation of AS association, which is the starting point for emerging and more specific therapies.

摘要

强直性脊柱炎(AS)是一种具有强烈遗传背景的脊柱慢性炎症性关节炎。通过全基因组关联研究(GWAS)确定的与AS相关的基因组位点的机制和功能理解仍然具有挑战性。染色体构象捕获(3C)及其衍生技术是最近的技术,在阐明空间基因组组织方面有很大帮助,并且在揭示疾病相关遗传变异的机制解释方面提供了巨大支持。三维(3D)基因组层次结构的扰动可能导致多种人类疾病,包括风湿性疾病。在这里,我们阐述了基因组组织领域的最新方法和相关发现,强调了3D基因组构象的不稳定性如何可能是风湿性疾病表型的原因之一。我们提出了一个新的观点,即3C方法在为风湿性疾病的GWAS结果提供信息方面的潜在包容性。3D基因组组织最终可能导致对AS关联进行更精确和全面的功能解释,这是新兴和更特异性疗法的起点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28cc/9905691/d2906e075d90/fgene-14-1129207-g001.jpg

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