双等位基因 MED16 变体会导致一种伴有智力障碍、运动迟缓以及颅面、心脏和四肢畸形的 MEDopathy。

IF 8.1 1区 生物学 Q1 GENETICS & HEREDITY
American journal of human genetics Pub Date : 2025-04-03 Epub Date: 2025-03-12 DOI:10.1016/j.ajhg.2025.02.016
Charlotte Guillouet, Valeria Agostini, Geneviève Baujat, Dario Cocciadiferro, Tommaso Pippucci, Marion Lesieur-Sebellin, Mathieu Georget, Ulrich Schatz, Christine Fauth, Raymond J Louie, Curtis Rogers, Jessica M Davis, Vassiliki Konstantopoulou, Johannes A Mayr, Arjan Bouman, Martina Wilke, Grace E VanNoy, Eleina M England, Kristen L Park, Kathleen Brown, Margarita Saenz, Antonio Novelli, Maria Cristina Digilio, Gioia Mastromoro, Mauro Ciro Antonio Rongioletti, Gerardo Piacentini, Rauan Kaiyrzhanov, Sughra Guliyeva, Lala Hasanova, Deborah Shears, Ishita Bhatnagar, Karen Stals, Oliver Klaas, Judit Horvath, Patrice Bouvagnet, P Dane Witmer, Gretchen MacCarrick, Katarina Cisarova, Jean-Marc Good, Svetlana Gorokhova, Odile Boute, Thomas Smol, Ange-Line Bruel, Olivier Patat, Julia R Broadbent, Tiong Y Tan, Natalie B Tan, Stanislas Lyonnet, Tiffany Busa, Claudio Graziano, Jeanne Amiel, Christopher T Gordon
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引用次数: 0

摘要

中介体复合体通过协调上游增强子与启动子基础转录机制的相互作用来调节蛋白质编码基因的转录。介质亚基的致病性变异通常导致具有不同临床表现的神经发育或神经退行性疾病,称为MEDopathies。在这里,我们报告了来自18个具有双等位基因MED16变异的家庭的25名个体,他们患有多发性先天性异常(MCAs)-智力残疾综合征。智力残疾、语言迟缓和/或不同程度的运动迟缓是恒定的,并与颅面缺陷(微颌后畸形、腭裂和耳前标记)、四肢异常和心脏缺陷(主要是法洛四联症)的不同组合有关。视力障碍、耳聋和磁共振成像(MRI)异常也很常见。鉴定的26个变异包括8个预测的蛋白质截断(3个基因内缺失,2个帧移位,1个无义和2个基本剪接位点变异)和18个影响保守残基的错义或帧内重复变异,表型严重程度与变异类型组合之间没有明确的相关性。三维模型表明,错义和重复变异可能对蛋白质的结构元件产生不稳定的影响。免疫荧光分析显示,17种变异中有16种的蛋白质从细胞核错定位到细胞质。与野生型相比,纯合子突变的med16斑马鱼表现出生长延迟和死亡率增加,而med16敲除小鼠在断奶前是致命的,这突出了med16对发育的保守要求。总的来说,我们描述了一种常染色体隐性mcas -智力残疾MEDopathy,强调了在神经发育过程中Mediator的重要性,并表明一些组织对某些亚基的缺失特别敏感。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bi-allelic MED16 variants cause a MEDopathy with intellectual disability, motor delay, and craniofacial, cardiac, and limb malformations.

The Mediator complex regulates protein-coding gene transcription by coordinating the interaction of upstream enhancers with the basal transcription machinery at the promoter. Pathogenic variants in Mediator subunits typically lead to neurodevelopmental or neurodegenerative disorders with variable clinical presentations, designated as MEDopathies. Here, we report the identification of 25 individuals from 18 families with bi-allelic MED16 variants who have a multiple congenital anomalies (MCAs)-intellectual disability syndrome. Intellectual disability, speech delay, and/or motor delay of variable severity were constant and associated with variable combinations of craniofacial defects (micro/retrognathia, cleft palate, and preauricular tags), anomalies of the extremities, and heart defects (predominantly tetralogy of Fallot). Visual impairment, deafness, and magnetic resonance imaging (MRI) abnormalities were also frequent. The 26 variants identified were comprised of eight predicted protein-truncating (three intragenic deletions, two frameshifts, and one nonsense and two essential splice site variants) and 18 missense or in-frame duplication variants affecting conserved residues, without clear correlation between phenotypic severity and variant type combination. Three-dimensional modeling indicated that the missense and duplication variants likely have a destabilizing effect on the structural elements of the protein. Immunofluorescence assays demonstrated protein mislocalization from the nucleus to the cytoplasm for 16 of the 17 variants studied. Homozygous mutant med16 zebrafish presented growth delay and increased mortality compared with wild-type fish, and Med16 knockout mice are preweaning lethal, highlighting the conserved requirement of MED16 for development. Overall, we describe an autosomal recessive MCAs-intellectual disability MEDopathy, emphasizing the importance of Mediator during neurodevelopment and suggesting that some tissues are particularly sensitive to the loss of certain subunits.

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来源期刊
CiteScore
14.70
自引率
4.10%
发文量
185
审稿时长
1 months
期刊介绍: The American Journal of Human Genetics (AJHG) is a monthly journal published by Cell Press, chosen by The American Society of Human Genetics (ASHG) as its premier publication starting from January 2008. AJHG represents Cell Press's first society-owned journal, and both ASHG and Cell Press anticipate significant synergies between AJHG content and that of other Cell Press titles.
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