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软骨的基因转录调控分析揭示骨关节炎的发病机制。

Genetic transcriptional regulation profiling of cartilage reveals pathogenesis of osteoarthritis.

作者信息

Tian Wen, Dong Shan-Shan, Jiang Feng, Zhang Jun-Qi, Wang Chen, He Chang-Yi, Hu Shou-Ye, Hao Ruo-Han, Song Hui-Miao, Gao Hui-Wu, An Ke, Zhu Dong-Li, Yang Zhi, Guo Yan, Yang Tie-Lin

机构信息

Key Laboratory of Biomedical Information Engineering of Ministry of Education, Biomedical Informatics & Genomics Center, School of Life Science and Technology, Xi'an Jiaotong University, Xi'an, Shaanxi 710049, PR China.

Honghui Hospital, Xi'an Jiaotong University, Xi'an, Shaanxi 710054, PR China.

出版信息

EBioMedicine. 2025 Jul;117:105821. doi: 10.1016/j.ebiom.2025.105821. Epub 2025 Jun 26.

Abstract

BACKGROUND

Genome-wide association studies (GWAS) have identified more than one hundred risk loci for osteoarthritis (OA). Identifying the effector genes and deciphering the underlying regulatory mechanisms are of great importance but remains challenging due to limited availability of OA-related tissue data. This study aims to address this issue by generating a cartilage expression quantitative trait loci (eQTLs) and a functional fine-mapping resource.

METHODS

We performed cis-eQTL analysis using genomics and cartilage transcriptomics data from 204 patients with OA (largest sample size to date). Cell type-interaction eQTL analysis (ci-eQTL) was conducted to explore the chondrocyte subtype dependency of eQTL effects. Co-localization analysis was used to nominate effector genes of OA GWAS risk loci. A deciphering pipeline was established to identify candidate causal variants in eQTL loci that regulate gene expression through the alteration of chromatin accessibility or disruption of transcription factors (TFs) binding to regulatory elements.

FINDINGS

We identified 3352 independent eQTLs for 3109 genes, 120 eQTL-gene pairs showed chondrocyte subtype dependency. We identified 19 new OA risk genes. We identified 117 causal eQTLs exhibiting allele-specific open chromatin (ASoC) and 547 eQTLs involved in transcription factor binding disruption (TBD). Functional validation showed that the T allele of the OA risk variant rs11750646 enhances the AR binding affinity to an open chromatin region, thereby promoting the expression of the OA-related gene PIK3R1.

INTERPRETATION

Our findings provide insights into the unique regulatory landscape of cartilage and elucidate potential mechanisms underlying OA pathogenesis.

FUNDING

This work was supported by National Natural Science Foundation of China (32470639, 82372458, and 82170896); Science Fund for Distinguished Young Scholars of Shaanxi Province (2025JC-JCQN-054); Innovation Capability Support Program of Shaanxi Province (2022TD-44, 2024RS-CXTD-86); Key Research and Development Project of Shaanxi Province (2023-YBSF-180); China Postdoctoral Science Foundation (2024M752561); and the Fundamental Research Funds for the Central Universities.

摘要

背景

全基因组关联研究(GWAS)已确定了100多个骨关节炎(OA)的风险位点。识别效应基因并解读潜在的调控机制至关重要,但由于OA相关组织数据有限,这仍然具有挑战性。本研究旨在通过生成软骨表达定量性状位点(eQTL)和功能精细定位资源来解决这一问题。

方法

我们使用来自204例OA患者的基因组学和软骨转录组学数据进行顺式eQTL分析(样本量为迄今为止最大)。进行细胞类型相互作用eQTL分析(ci-eQTL)以探索eQTL效应的软骨细胞亚型依赖性。共定位分析用于确定OA GWAS风险位点的效应基因。建立了一个解读流程,以识别eQTL位点中通过改变染色质可及性或破坏转录因子(TF)与调控元件的结合来调节基因表达的候选因果变异。

研究结果

我们为3109个基因鉴定了3352个独立的eQTL,120个eQTL-基因对显示出软骨细胞亚型依赖性。我们鉴定出19个新的OA风险基因。我们鉴定出117个表现出等位基因特异性开放染色质(ASoC)的因果eQTL和547个参与转录因子结合破坏(TBD)的eQTL。功能验证表明,OA风险变异rs11750646的T等位基因增强了AR与开放染色质区域的结合亲和力,从而促进了OA相关基因PIK3R1的表达。

解读

我们的研究结果为软骨独特的调控格局提供了见解,并阐明了OA发病机制的潜在机制。

资助

本研究得到中国国家自然科学基金(32470639、82372458和82170896);陕西省杰出青年科学基金(2025JC-JCQN-054);陕西省创新能力支持计划(2022TD-44、2024RS-CXTD-86);陕西省重点研发计划项目(2023-YBSF-180);中国博士后科学基金(2024M752561);以及中央高校基本科研业务费专项资金的资助。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2934/12278629/601dccc247ce/gr1.jpg

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