Meyer Néva P, Roelink Henk
Molecular and Cellular Biology Program, Department of Biological Structure, Center for Developmental Biology, University of Washington, Box 357420, Seattle, WA 98195, USA.
Dev Biol. 2003 May 15;257(2):343-55. doi: 10.1016/s0012-1606(03)00065-4.
A concentration gradient of Shh is thought to pattern the ventral neural tube, and these ventral cell types are absent in shh-/- mice. Based on in vitro and genetic studies, the zinc finger-containing transcription factors Gli 1, 2, and 3 are mediators of the Shh intracellular response. The floorplate and adjacent cell types are absent in gli1-/-;gli2-/- mice, but part of the Shh-/- phenotype in the neural tube is alleviated in the Shh-/-;gli3-/- double mutant. This is consistent with the predicted role of Gli3 as a repressor of the Shh response. Gli3 repressor activity is blocked by Shh. In order to test the role of the repressor form of Gli3 in the neural tube, a truncated version of Gli3 (Gli3R*) was designed to mimic a Pallister Hall allele. Gli3R* acts as a constitutive repressor independent of Shh signaling. Misexpression of Gli3R* in the chick neural tube caused a ventral expansion of class-I, dorsal progenitor proteins and a loss of class-II, ventral progenitor proteins consistent with expected activity as a repressor of the Shh response. Activation of the BMP response is sufficient to maintain gli3 expression in neural plate explants, which might be a mechanism by which BMPs antagonize the Shh response.
Shh浓度梯度被认为可对腹侧神经管进行模式化,而在shh基因敲除小鼠中不存在这些腹侧细胞类型。基于体外和遗传学研究,含锌指的转录因子Gli 1、2和3是Shh细胞内反应的介质。在gli1基因敲除;gli2基因敲除小鼠中,底板和相邻细胞类型缺失,但在Shh基因敲除;gli3基因敲除双突变体中,神经管中部分Shh基因敲除表型得到缓解。这与Gli3作为Shh反应抑制因子的预测作用一致。Gli3抑制活性被Shh阻断。为了测试Gli3抑制形式在神经管中的作用,设计了一种Gli3截短版本(Gli3R*)来模拟帕利斯特·霍尔等位基因。Gli3R作为一种独立于Shh信号传导的组成型抑制因子发挥作用。Gli3R在鸡神经管中的错误表达导致I类背侧祖细胞蛋白腹侧扩展和II类腹侧祖细胞蛋白缺失,这与作为Shh反应抑制因子的预期活性一致。BMP反应的激活足以维持神经板外植体中gli3的表达,这可能是BMP拮抗Shh反应的一种机制。