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染色质环连将目标基因与皮肤特征的遗传风险位点联系起来。

Chromatin Looping Links Target Genes with Genetic Risk Loci for Dermatological Traits.

机构信息

Centre for Genetics and Genomics Versus Arthritis, Division of Musculoskeletal and Dermatological Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, United Kingdom.

Centre for Genetics and Genomics Versus Arthritis, Division of Musculoskeletal and Dermatological Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, United Kingdom; Dermatology Centre, Salford Royal NHS Foundation Trust, NIHR Manchester Biomedical Research Centre, Manchester Academic Health Science Centre, Manchester, United Kingdom.

出版信息

J Invest Dermatol. 2021 Aug;141(8):1975-1984. doi: 10.1016/j.jid.2021.01.015. Epub 2021 Feb 17.

Abstract

Chromatin looping between regulatory elements and gene promoters presents a potential mechanism whereby disease risk variants affect their target genes. In this study, we use H3K27ac HiChIP, a method for assaying the active chromatin interactome in two cell lines: keratinocytes and skin lymphoma-derived CD8+ T cells. We integrate public datasets for a lymphoblastoid cell line and primary CD4+ T cells and identify gene targets at risk loci for skin-related disorders. Interacting genes enrich for pathways of known importance in each trait, such as cytokine response (psoriatic arthritis and psoriasis) and replicative senescence (melanoma). We show examples of how our analysis can inform changes in the current understanding of multiple psoriasis-associated risk loci. For example, the variant rs10794648, which is generally assigned to IFNLR1, was linked to GRHL3, a gene essential in skin repair and development, in our dataset. Our findings, therefore, indicate a renewed importance of skin-related factors in the risk of disease.

摘要

染色质环在调控元件和基因启动子之间形成一种潜在的机制,使疾病风险变异影响其靶基因。在这项研究中,我们使用 H3K27ac HiChIP 方法在两种细胞系(角质形成细胞和皮肤淋巴瘤衍生的 CD8+T 细胞)中检测活性染色质互作组。我们整合了淋巴母细胞系和原代 CD4+T 细胞的公共数据集,并鉴定了与皮肤相关疾病风险位点相关的基因靶标。相互作用的基因富集了已知在每个特征中具有重要作用的途径,如细胞因子反应(银屑病关节炎和银屑病)和复制性衰老(黑色素瘤)。我们展示了我们的分析如何为多种银屑病相关风险位点的现有理解提供信息。例如,通常分配给 IFNLR1 的变体 rs10794648 在我们的数据集与 GRHL3 相关联,GRHL3 是皮肤修复和发育所必需的基因。因此,我们的发现表明皮肤相关因素在疾病风险中的重要性再次得到重视。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f91/8315765/ff38c170fbdb/fx1.jpg

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