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CHAMP1基因中的新生致病性变异与全面发育迟缓、智力障碍和面部畸形特征有关。

De novo pathogenic variants in CHAMP1 are associated with global developmental delay, intellectual disability, and dysmorphic facial features.

作者信息

Tanaka Akemi J, Cho Megan T, Retterer Kyle, Jones Julie R, Nowak Catherine, Douglas Jessica, Jiang Yong-Hui, McConkie-Rosell Allyn, Schaefer G Bradley, Kaylor Julie, Rahman Omar A, Telegrafi Aida, Friedman Bethany, Douglas Ganka, Monaghan Kristin G, Chung Wendy K

机构信息

Department of Pediatrics, Columbia University Medical Center, New York, New York 10032, USA;

GeneDx, Gaithersburg, Maryland 20877, USA;

出版信息

Cold Spring Harb Mol Case Stud. 2016 Jan;2(1):a000661. doi: 10.1101/mcs.a000661.

Abstract

We identified five unrelated individuals with significant global developmental delay and intellectual disability (ID), dysmorphic facial features and frequent microcephaly, and de novo predicted loss-of-function variants in chromosome alignment maintaining phosphoprotein 1 (CHAMP1). Our findings are consistent with recently reported de novo mutations in CHAMP1 in five other individuals with similar features. CHAMP1 is a zinc finger protein involved in kinetochore-microtubule attachment and is required for regulating the proper alignment of chromosomes during metaphase in mitosis. Mutations in CHAMP1 may affect cell division and hence brain development and function, resulting in developmental delay and ID.

摘要

我们鉴定出了五名无亲缘关系的个体,他们均有明显的全面发育迟缓及智力残疾(ID)、面部畸形特征且常伴有小头畸形,并且在染色体排列维持磷蛋白1(CHAMP1)中存在从头预测的功能丧失变异。我们的发现与最近报道的另外五名具有相似特征个体中CHAMP1的从头突变一致。CHAMP1是一种锌指蛋白,参与动粒-微管附着,并且是有丝分裂中期调节染色体正确排列所必需的。CHAMP1中的突变可能影响细胞分裂,并因此影响大脑发育和功能,导致发育迟缓及智力残疾。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/449e/4849844/dc144370d1bc/TanakaMCS000661_F1.jpg

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