Embryonic Development of the Cerebellum

超出所提供的空间。我们以前的工作集中在胚胎小脑颗粒细胞的规格。在这里，我们希望把注意力转向小脑的另一个主要神经元，浦肯野细胞和深部神经元。该项目的总体目标是确定四类转录因子的地形表达，LIM同源结构域基因（Lhxl, Lhx3， Lhx5和Lhx9），基本螺旋-环-螺旋基因（Math1, Mash1, Ngnl, Ngn2），配对盒包含基因（Pax2）和甚至跳过基因（Evxl,2）在胚胎小脑原基的浦金野和深层神经元祖细胞群体中，并使用这些标记来检查塑造细胞命运规范的因素。局部诱导因子、bmp对基因表达和细胞特异模式的作用将在鸡胚和Dreher突变小鼠的基因表达研究中得到验证。首先，我们将定义动物和鸟类胚胎中的基因表达模式，重点关注深度神经元和浦肯野细胞产生的时间周期。我们将通过研究另一个项目中产生的Lhxl、Lhx3、Lhx5、Lhx9、Math1、Mash1、Ngnl、Ngn2和Evxl的BAC转基因小鼠来进一步完善我们的分析。其次，我们将研究Dreher突变小鼠，因为它遭受BMPs的损失，并使用禽胚胎的卵电穿孔来确定BMP6的作用。转录因子表达模式中的BMP7和GDF7。最后，我们将研究这些转录因子在小脑细胞分化中的功能，通过分析小鼠靶向零突变和将morpholino反义寡核苷酸转染到禽类胚胎中。网站性能 ======================================== 节结束 ===========================================

EXCEED THE SPACE _ROVIDED. Our previous work has focused on the specification of granule cells in the embryonic cerebellum. Here we wish to turn our attention to the other principal neuron of the cerebellum, the Purkinje cell and to the deep neurons. The overall aim of this project is to determine the topographic expression of four classes of transcription factors, LIM homeodomain genes (Lhxl, Lhx3, Lhx5, and Lhx9), basic helix-loop-helix genes (Math1, Mash1, Ngnl, Ngn2), Paired box containing genes (Pax2) and Even-Skipped genes (Evxl,2) in Purkinje and deep neuron progenitor cell populations in the embryonic cerebellar primordium, and to use these markers to examine factors that shape cell fate specification. The action of local inductive factors, BMPs on gene expression and cell specification patterning will be tested in gone expression studies in the chick embryo and in the Dreher mutant mouse. First, we will define patterns of gene expression in mudne and avian embryos focusing on the time periods when deep neurons and Purkinje cells are generated. We will further refine our analysis by studying BAC transgenic mice for Lhxl, Lhx3, Lhx5, Lhx9, Math1, Mash1, Ngnl, Ngn2 and Evxl generated in another project. Second, we will study the Dreher mutant mouse, because it suffers a loss of BMPs, and use in ovo electroporation in avian embryos to define the role of BMP6. BMP7 and GDF7 in transcription factor expression patterns. Finally, we will study the function of these transcription factors in cerebellar cell differentiation by analyzing mice with targeted null mutations and by transfecting morpholino antisense oligonucleotides into avian embryos. PERFORMANCE SITE ========================================Section End===========================================