Foxp-regulated signaling pathways in brain development

项目摘要/摘要 单个疾病相关基因对大脑发育的贡献仍然未知。长期的 我们实验室的目标是阐明被干扰的分子信号通路的交集 神经发育障碍与那些对大脑发育的特定方面很重要的通路有关。 FOXP转录因子家族的两个成员，Foxp1和FOXP2，已被认为与单基因 智力残疾、自闭症谱系障碍以及特定的言语和语言缺陷。中的变体 FOXP1或FOXP2是与自闭症谱系障碍相关的最重要的基因之一。我们 先前研究表明，Foxp1和Foxp2对皮质和纹状体的发育都有重要贡献。 我们通过对基因表达、电生理学和行为的研究将这些发育变化联系起来。我们 利用新获得的单细胞RNA进一步鉴定基因表达的非细胞自主变化 测序技术。根据这些数据，支持这一提议的中心假设是Foxp1 和Foxp2是转录信号级联的关键协调者，以一种特定于细胞类型的方式 对神经元功能很重要，并有患自闭症等神经发育障碍的风险。我们 建议通过使用啮齿动物模型来确定这些细胞类型在发育中的皮质中的特定贡献 3个具体目标：1)确定Foxp1调控的细胞类型特异性基因表达程序 2)确定Foxp2调控的细胞类型特异性基因表达程序。 以及3)评估Foxp1和Foxp2在细胞类型特异性活动依赖神经元中的作用 功能。总之，这些目标将描绘Foxp1和Foxp2对皮质的细胞类型贡献 发展。啮齿动物模型和特定细胞类型的基因组数据集将提供对基本的 控制正常哺乳动物大脑发育的分子机制。

Project Summary/Abstract The contribution of individual disease-relevant genes to brain development still remains unknown. The long-term goal of our laboratory is to elucidate the intersection of molecular signaling pathways that are disrupted in neurodevelopmental disorders with those pathways that are important for specific aspects of brain development. Two members of the FOXP family of transcription factors, FOXP1 and FOXP2, have been linked to monogenetic forms of intellectual disability, autism spectrum disorders, and specific speech and language deficits. Variants in FOXP1 or FOXP2 are among the most significant genes associated with autism spectrum disorders. We previously showed that Foxp1 and Foxp2 both have significant contributions to cortical and striatal development. We linked these developmental changes via studies of gene expression, electrophysiology, and behaviors. We further identified non-cell-autonomous changes in gene expression using newly available single-cell RNA- sequencing technology. Based on these data, the central hypothesis driving this proposal is that Foxp1 and Foxp2 are key orchestrators of transcriptional signaling cascades in a cell type-specific manner that are important for neuronal function and are at risk in neurodevelopmental disorders such as autism. We propose to identify these cell type-specific contributions in the developing cortex by using rodent models through three specific aims: 1) Determine the cell type-specific gene expression programs regulated by Foxp1 in the developing cortex; 2) Determine the cell type-specific gene expression programs regulated by Foxp2 in the developing cortex; and 3) Assess the role of Foxp1 and Foxp2 in cell type-specific activity-dependent neuronal function. Together, these aims will delineate the cell type contribution of both Foxp1 and Foxp2 to cortical development. The rodent models and cell-type specific genomic datasets will aprovide insight into the basic molecular mechanisms governing normal mammalian brain development.