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与自闭症和智力残疾相关的MYT1L突变会改变人类皮质中间神经元的分化、成熟和生理功能。

Autism- and intellectual disability-associated MYT1L mutation alters human cortical interneuron differentiation, maturation, and physiology.

作者信息

Prakasam Ramachandran, Determan Julianna, Chapman Gareth, Narasimhan Mishka, Shen Renata, Saleh Maamoon, Kaushik Komal, Gontarz Paul, Meganathan Kesavan, Hakim Bilal, Zhang Bo, Huettner James E, Kroll Kristen L

机构信息

Department of Developmental Biology, Washington University School of Medicine, St Louis, MO 63110, USA.

Department of Cell Biology and Physiology, Washington University School of Medicine, St Louis, MO 63110, USA.

出版信息

Stem Cell Reports. 2025 Mar 11;20(3):102421. doi: 10.1016/j.stemcr.2025.102421. Epub 2025 Feb 27.

Abstract

Myelin transcription factor 1 like (MYT1L) is a neuronal transcription factor highly expressed in the developing and adult brain, and, while pathogenic MYT1L mutations cause neurodevelopmental disorders, these have not been characterized in human models of neurodevelopment. Here, we modeled the consequences of pathogenic MYT1L mutation using human stem cell-derived cortical neurons, demonstrating that MYT1L mutation alters the differentiation trajectory, increasing neuronal gene expression, morphological complexity, and synapse production. We also examined consequences of MYT1L mutation in mature cortical interneurons, identifying hallmarks of impaired neuronal identity and maturation and correspondingly altered channel expression and electrophysiological properties. Finally, by defining MYT1L genome-wide occupancy in cortical interneurons, we identified direct MYT1L targets likely to mediate these phenotypes. Together, this work elucidates new MYT1L requirements for human cortical interneuron development and demonstrates how pathogenic MYT1L mutation perturbs this developmental program, contributing to the etiology of neurodevelopmental disorders.

摘要

髓磷脂转录因子1样蛋白(MYT1L)是一种在发育中的大脑和成年大脑中高度表达的神经元转录因子。虽然致病性MYT1L突变会导致神经发育障碍,但这些在神经发育的人类模型中尚未得到表征。在这里,我们使用人类干细胞衍生的皮质神经元对致病性MYT1L突变的后果进行建模,证明MYT1L突变会改变分化轨迹,增加神经元基因表达、形态复杂性和突触产生。我们还研究了MYT1L突变在成熟皮质中间神经元中的后果,确定了神经元身份和成熟受损的特征,并相应地改变了通道表达和电生理特性。最后,通过定义MYT1L在皮质中间神经元中的全基因组占据情况,我们确定了可能介导这些表型的直接MYT1L靶标。总之,这项工作阐明了人类皮质中间神经元发育对MYT1L的新需求,并证明了致病性MYT1L突变如何扰乱这一发育程序,从而导致神经发育障碍的病因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6e9/11960533/e773faecf619/gr1.jpg

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