Single-cell RNA Sequencing of Peripheral Blood Links Cell-Type-specific Regulation of Splicing to Autoimmune and Inflammatory Diseases

Chi Tian, Yuntian Zhang, Yihan Tong, Kian Hong Kock,Donald Yuhui Sim, Fei Liu, Jiaqi Dong, Zhixuan Jing, Wenjing Wang, Junbin Gao,Le Min Tan,Kyung Yeon Han,Yoshihiko Tomofuji,Masahiro Nakano, Eliora Violain Buyamin, Radhika Sonthalia,Yoshinari Ando,Hiroaki Hatano,Kyuto Sonehara, Asian Immune Diversity Atlas Network, Xin Jin, Marie Loh,John Chambers大牛学者, Chung-Chau Hon,Murim Choi大牛学者,Jong-Eun Park,Kazuyoshi Ishigaki,Tomohisa Okamura,Keishi Fujio, Yukinori Okada, Woong-Yang Park, Jay W Shin,Xavier Roca, Shyam Prabhakar,Boxiang Liu

Nature genetics(2024)

引用 0|浏览0
摘要
Alternative splicing contributes to complex traits, but whether this differs in trait-relevant cell types across diverse genetic ancestries is unclear. Here we describe cell-type-specific, sex-biased and ancestry-biased alternative splicing in ~1 M peripheral blood mononuclear cells from 474 healthy donors from the Asian Immune Diversity Atlas. We identify widespread sex-biased and ancestry-biased differential splicing, most of which is cell-type-specific. We identify 11,577 independent cis-splicing quantitative trait loci (sQTLs), 607 trans-sGenes and 107 dynamic sQTLs. Colocalization between cis-eQTLs and trans-sQTLs revealed a cell-type-specific regulatory relationship between HNRNPLL and PTPRC. We observed an enrichment of cis-sQTL effects in autoimmune and inflammatory disease heritability. Specifically, we functionally validated an Asian-specific sQTL disrupting the 5' splice site of TCHP exon 4 that putatively modulates the risk of Graves' disease in East Asian populations. Our work highlights the impact of ancestral diversity on splicing and provides a roadmap to dissect its role in complex diseases at single-cell resolution.
更多
查看译文
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
0
您的评分 :

暂无评分

数据免责声明
页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果,我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问,可以通过电子邮件方式联系我们:report@aminer.cn