Sun Wenmin, Xiong Dan, Ouyang Jiamin, Xiao Xueshan, Jiang Yi, Wang Yingwei, Li Shiqiang, Xie Ziying, Wang Junwen, Tang Zhonghui, Zhang Qingjiong
State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Guangzhou, 510060, China.
Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, 510080, China.
Nat Commun. 2024 Jun 13;15(1):5048. doi: 10.1038/s41467-024-49376-w.
Despite the advent of genomic sequencing, molecular diagnosis remains unsolved in approximately half of patients with Mendelian disorders, largely due to unclarified functions of noncoding regions and the difficulty in identifying complex structural variations. In this study, we map a unique form of central iris hypoplasia in a large family to 6q15-q23.3 and 18p11.31-q12.1 using a genome-wide linkage scan. Long-read sequencing reveals a balanced translocation t(6;18)(q22.31;p11.22) with intergenic breakpoints. By performing Hi-C on induced pluripotent stem cells from a patient, we identify two chromatin topologically associating domains spanning across the breakpoints. These alterations lead the ectopic chromatin interactions between APCDD1 on chromosome 18 and enhancers on chromosome 6, resulting in upregulation of APCDD1. Notably, APCDD1 is specifically localized in the iris of human eyes. Our findings demonstrate that noncoding structural variations can lead to Mendelian diseases by disrupting the 3D genome structure and resulting in altered gene expression.
尽管基因组测序技术已经问世,但在大约一半的孟德尔疾病患者中,分子诊断问题仍未得到解决,这主要是由于非编码区功能尚不清楚,以及识别复杂结构变异存在困难。在本研究中,我们通过全基因组连锁扫描,将一个大家庭中一种独特形式的中央虹膜发育不全定位到6q15-q23.3和18p11.31-q12.1。长读长测序揭示了一个具有基因间断点的平衡易位t(6;18)(q22.31;p11.22)。通过对患者的诱导多能干细胞进行Hi-C分析,我们确定了两个跨越断点的染色质拓扑关联结构域。这些改变导致18号染色体上的APCDD1与6号染色体上的增强子之间发生异位染色质相互作用,从而导致APCDD1上调。值得注意的是,APCDD1特异性定位于人眼的虹膜中。我们的研究结果表明,非编码结构变异可通过破坏三维基因组结构并导致基因表达改变而引发孟德尔疾病。