增强子
表型
斑马鱼
下调和上调
遗传学
基因
生物
基因缺失
基因表达调控
表观遗传学
遗传异质性
转录调控
转录因子
细胞生物学
遗传关联
候选基因
萤光素酶类
体内
基因表达
生物信息学
突变
遗传倾向
作者
Xiaofeng Li,Dandan Li,Shu Lou,Junyan Lin,Yue Gao,Barbara Vona,Congbo Mi,Lin Wang,Lan Ma,Mulong Du,Yongchu Pan
出处
期刊:Cell Reports
[Cell Press]
日期:2025-10-01
卷期号:44 (10): 116377-116377
被引量:1
标识
DOI:10.1016/j.celrep.2025.116377
摘要
Genome-wide association studies have identified numerous loci associated with nonsyndromic cleft lip with/without cleft palate (nsCL/P). However, the causal genes within these loci remain to be systematically investigated. Through a multiomics screening strategy, we identified 20 candidate genes, with ARID3B emerging as the most significant risk gene for nsCL/P. Focusing on the ARID3B locus, we found a casual variant at rs1821848 that diminished the binding affinity of NR2C2, resulting in the upregulation of ARID3B. Notably, we observed the formation of ARID3B granules through liquid-liquid phase separation (LLPS) both in vivo and in vitro. This ARID3B-mediated LLPS could essentially recruit coactivators SMAD2/3 and establish enhancer activity necessary for initiating the gene profile related to nsCL/P. Ultimately, disrupting the LLPS of arid3b effectively rescued migration, apoptosis, and phenotype deficits in zebrafish models. This study systematically revealed biological functions of both rs1821848 and ARID3B during nsCL/P development.
科研通智能强力驱动
Strongly Powered by AbleSci AI