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Prioritizing de novo potential non-canonical splicing variants in neurodevelopmental disorders

小基因 RNA剪接 生物 选择性拼接 遗传学 基因 生物信息学 信使核糖核酸 核糖核酸
作者
Kuokuo Li,Junyan Xiao,Zhengbao Ling,Tengfei Luo,Junwu Xiong,Qian Chen,Lijie Dong,Yijing Wang,Xiaomeng Wang,Zhaoxin Jiang,Lu Xia,Zhen Yu,Rong Hua,Rui Guo,Dongdong Tang,Mingrong Lv,Aojie Lian,Bin Li,Guihu Zhao,Xiaojin He,Kun Xia,Yunxia Cao,Jinchen Li
出处
期刊:EBioMedicine [Elsevier]
卷期号:99: 104928-104928 被引量:3
标识
DOI:10.1016/j.ebiom.2023.104928
摘要

BackgroundGenomic variants outside of the canonical splicing site (±2) may generate abnormal mRNA splicing, which are defined as non-canonical splicing variants (NCSVs). However, the clinical interpretation of NCSVs in neurodevelopmental disorders (NDDs) is largely unknown.MethodsWe investigated the contribution of NCSVs to NDDs from 345,787 de novo variants (DNVs) in 47,574 patients with NDDs. We performed functional enrichment and protein–protein interaction analysis to assess the association between genes carrying prioritised NCSVs and NDDs. Minigene was used to validate the impact of NCSVs on mRNA splicing.FindingsWe observed significantly more NCSVs (p = 0.02, odds ratio [OR] = 2.05) among patients with NDD than in controls. Both canonical splicing variants (CSVs) and NCSVs contributed to an equal proportion of patients with NDD (0.76% vs. 0.82%). The candidate genes carrying NCSVs were associated with glutamatergic synapse and chromatin remodelling. Minigene successfully validated 59 of 79 (74.68%) NCSVs that led to abnormal splicing in 40 candidate genes, and 9 of the genes (ARID1B, KAT6B, TCF4, SMARCA2, SHANK3, PDHA1, WDR45, SCN2A, SYNGAP1) harboured recurrent NCSVs with the same variant present in more than two unrelated patients with NDD. Moreover, 36 of 59 (61.02%) NCSVs are novel clinically relevant variants, including 34 unreported and 2 clinically conflicting interpretations or of uncertain significance NCSVs in the ClinVar database.InterpretationThis study highlights the common pathology and clinical importance of NCSVs in unsolved patients with NDD.FundingThe present study was funded by grants from the National Natural Science Foundation of China, China Postdoctoral Science Foundation, the Hunan Youth Science and Technology Innovation Talent Project, the Provincial Natural Science Foundation of Hunan, The Scientific Research Program of FuRong laboratory, and the Natural Science Project of the University of Anhui Province
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