Key Laboratory of Molecular Biophysics of the Ministry of Education, College of Life Science and Technology, Center for Human Genome Research and Cardio-X Institute, Huazhong University of Science and Technology, Wuhan, 430074, China.
Department of Molecular Cardiology, Center for Cardiovascular Genetics, Cleveland Clinic Lerner Research Institute, Cleveland, OH, 44195, USA.
Mol Genet Genomics. 2018 Jun;293(3):699-710. doi: 10.1007/s00438-018-1417-6. Epub 2018 Jan 10.
We investigated an Amish family in which three siblings presented with an early-onset childhood retinal dystrophy inherited in an autosomal recessive fashion. Genome-wide linkage analysis identified significant linkage to marker D2S2216 on 2q11 with a two-point LOD score of 1.95 and a multi-point LOD score of 3.76. Whole exome sequencing was then performed for the three affected individuals and identified a homozygous nonsense mutation (c.C1813T, p.R605X) in the cyclin and CBS domain divalent metal cation transport mediator 4 (CNNM4) gene located within the 2p14-2q14 Jalili syndrome locus. The initial assessment and collection of the family were performed before the clinical delineation of Jalili syndrome. Another assessment was made after the discovery of the responsible gene and the dental abnormalities characteristic of Jalili syndrome were retrospectively identified. The p.R605X mutation represents the first probable founder mutation of Jalili syndrome identified in the Amish community. The molecular mechanism underlying Jalili syndrome is unknown. Here we show that CNNM4 interacts with IQCB1, which causes Leber congenital amaurosis (LCA) when mutated. A truncated CNNM4 protein starting at R605 significantly increased the rate of apoptosis, and significantly increased the interaction between CNNM4 and IQCB1. Mutation p.R605X may cause Jalili syndrome by a nonsense-mediated decay mechanism, affecting the function of IQCB1 and apoptosis, or both. Our data, for the first time, functionally link Jalili syndrome gene CNNM4 to LCA gene IQCB1, providing important insights into the molecular pathogenic mechanism of retinal dystrophy in Jalili syndrome.
我们调查了一个阿米什家族,该家族的三个兄弟姐妹表现出常染色体隐性遗传的早发性儿童视网膜营养不良。全基因组连锁分析确定与 2q11 上的标记 D2S2216 存在显著连锁,两点 LOD 得分为 1.95,多点 LOD 得分为 3.76。然后对 3 名受影响个体进行全外显子组测序,发现位于 2p14-2q14 Jalili 综合征基因座内的细胞周期蛋白和 CBS 域二价金属阳离子转运介质 4(CNNM4)基因存在纯合无义突变(c.C1813T,p.R605X)。在 Jalili 综合征临床描述之前,对该家族进行了初步评估和样本收集。在发现相关基因后,进行了另一次评估,并回顾性确定了 Jalili 综合征的特征性牙齿异常。p.R605X 突变代表在阿米什社区中发现的 Jalili 综合征的第一个可能的创始人突变。Jalili 综合征的分子机制尚不清楚。在这里,我们展示了 CNNM4 与 IQCB1 相互作用,当 IQCB1 发生突变时会导致莱伯先天性黑蒙(LCA)。从 R605 开始的截断 CNNM4 蛋白显著增加了细胞凋亡率,并显著增加了 CNNM4 与 IQCB1 之间的相互作用。突变 p.R605X 可能通过无义介导的衰变机制导致 Jalili 综合征,影响 IQCB1 和细胞凋亡的功能,或两者兼而有之。我们的数据首次将 Jalili 综合征基因 CNNM4 与 LCA 基因 IQCB1 功能联系起来,为 Jalili 综合征视网膜营养不良的分子发病机制提供了重要的见解。