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ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity

机译:ZC4H2突变与中枢和外周突触可塑性受损有关,与多发性先天性关节炎和智力障碍有关

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摘要

Arthrogryposis multiplex congenita (AMC) is caused by heterogeneous pathologies leading to multiple antenatal joint contractures through fetal akinesia. Understanding the pathophysiology of this disorder is important for clinical care of the affected individuals and genetic counseling of the families. We thus aimed to establish the genetic basis of an AMC subtype that is associated with multiple dysmorphic features and intellectual disability (ID). We used haplotype analysis, next-generation sequencing, array comparative genomic hybridization, and chromosome breakpoint mapping to identify the pathogenic mutations in families and simplex cases. Suspected disease variants were verified by cosegregation analysis. We identified disease-causing mutations in the zinc-finger gene ZC4H2 in four families affected by X-linked AMC plus ID and one family affected by cerebral palsy. Several heterozygous females were also affected, but to a lesser degree. Furthermore, we found two ZC4H2 deletions and one rearrangement in two female and one male unrelated simplex cases, respectively. In mouse primary hippocampal neurons, transiently produced ZC4H2 localized to the postsynaptic compartment of excitatory synapses, and the altered protein influenced dendritic spine density. In zebrafish, antisense-morpholino-mediated zc4h2 knockdown caused abnormal swimming and impaired α-motoneuron development. All missense mutations identified herein failed to rescue the swimming defect of zebrafish morphants. We conclude that ZC4H2 point mutations, rearrangements, and small deletions cause a clinically variable broad-spectrum neurodevelopmental disorder of the central and peripheral nervous systems in both familial and simplex cases of both sexes. Our results highlight the importance of ZC4H2 for genetic testing of individuals presenting with ID plus muscle weakness and minor or major forms of AMC
机译:多发性先天性关节炎(AMC)是由异质性病理导致的,通过胎儿运动障碍导致多个产前关节挛缩。了解这种疾病的病理生理学对受影响个体的临床护理和家庭遗传咨询很重要。因此,我们旨在建立与多种畸形特征和智力障碍(ID)相关的AMC亚型的遗传基础。我们使用单倍型分析,下一代测序,阵列比较基因组杂交和染色体断点作图,以鉴定家庭和单纯病例中的致病突变。通过共同偏析分析验证了疑似疾病变体。我们在四个受X连锁AMC加ID影响的家庭和一个受脑瘫影响的家庭中发现了锌指基因ZC4H2的致病突变。几位杂合子雌性也受到影响,但程度较小。此外,我们分别在两名女性和一名男性无关的单纯形病例中发现了两个ZC4H2缺失和一个重排。在小鼠原代海马神经元中,瞬时产生的ZC4H2定位于兴奋性突触的突触后区室,并且改变的蛋白质影响树突棘密度。在斑马鱼中,反义吗啉代介导的zc4h2敲低导致游泳异常和α-运动神经元发育受损。本文鉴定的所有错义突变均未能挽救斑马鱼吗啡酮的游泳缺陷。我们得出的结论是,ZC4H2点突变,重排和小缺失会导致中性和外周神经系统的临床可变的广谱神经发育障碍,无论是家族性还是单纯性。我们的结果凸显了ZC4H2对于具有ID,肌肉无力和AMC的次要或主要形式的个体进行基因测试的重要性

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