Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Raymond G. Perelman Center for Cellular & Molecular Therapeutics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Mov Disord. 2021 Dec;36(12):2780-2794. doi: 10.1002/mds.28750. Epub 2021 Aug 17.
X-linked dystonia parkinsonism is a generalized, progressive dystonia followed by parkinsonism with onset in adulthood and accompanied by striatal neurodegeneration. Causative mutations are located in a noncoding region of the TATA-box binding protein-associated factor 1 (TAF1) gene and result in aberrant splicing. There are 2 major TAF1 isoforms that may be decreased in symptomatic patients, including the ubiquitously expressed canonical cTAF1 and the neuronal-specific nTAF1.
The objective of this study was to determine the behavioral and transcriptomic effects of decreased cTAF1 and/or nTAF1 in vivo.
We generated adeno-associated viral (AAV) vectors encoding microRNAs targeting Taf1 in a splice-isoform selective manner. We performed intracerebroventricular viral injections in newborn mice and rats and intrastriatal infusions in 3-week-old rats. The effects of Taf1 knockdown were assayed at 4 months of age with evaluation of motor function, histology, and RNA sequencing of the striatum, followed by its validation.
We report motor deficits in all cohorts, more pronounced in animals injected at P0, in which we also identified transcriptomic alterations in multiple neuronal pathways, including the cholinergic synapse. In both species, we show a reduced number of striatal cholinergic interneurons and their marker mRNAs after Taf1 knockdown in the newborn.
This study provides novel information regarding the requirement for TAF1 in the postnatal maintenance of striatal cholinergic neurons, the dysfunction of which is involved in other inherited forms of dystonia. © 2021 International Parkinson and Movement Disorder Society.
X 连锁型肌张力障碍帕金森病是一种以成年期起病、进行性加重的全身性肌张力障碍,伴有帕金森病,伴纹状体神经退行性变。致病突变位于 TATA 框结合蛋白相关因子 1(TAF1)基因的非编码区,导致剪接异常。有 2 种主要的 TAF1 同工型可能在有症状的患者中减少,包括普遍表达的经典 cTAF1 和神经元特异性 nTAF1。
本研究旨在确定体内 cTAF1 和/或 nTAF1 减少的行为和转录组学效应。
我们生成了腺相关病毒(AAV)载体,以剪接异构体选择性的方式靶向 Taf1 的 microRNAs。我们在新生小鼠和大鼠的侧脑室中进行病毒注射,在 3 周龄大鼠的纹状体中进行脑内注射。用 4 个月大的动物评估运动功能、组织学和纹状体的 RNA 测序来检测 Taf1 敲低的效果,随后进行验证。
我们报告了所有队列的运动缺陷,在 P0 时注射的动物更为明显,其中我们还鉴定了多个神经元通路(包括胆碱能突触)的转录组改变。在这两种物种中,我们在新生鼠中观察到 Taf1 敲低后纹状体胆碱能中间神经元及其标志物 mRNAs 的数量减少。
本研究提供了关于 TAF1 在纹状体胆碱能神经元出生后维持中的必要性的新信息,其功能障碍与其他遗传性肌张力障碍有关。