Cau E, Gradwohl G, Casarosa S, Kageyama R, Guillemot F
IGBMC, CNRS/INSERM/Université Louis Pasteur, BP 163, CU de Strasbourg, France.
Development. 2000 Jun;127(11):2323-32. doi: 10.1242/dev.127.11.2323.
We have characterised the functions of the bHLH transcriptional repressors HES1 and HES5 in neurogenesis, using the development of the olfactory placodes in mouse embryos as a model. Hes1 and Hes5 are expressed with distinct patterns in the olfactory placodes and are subject to different regulatory mechanisms. Hes1 is expressed in a broad placodal domain, which is maintained in absence of the neural determination gene Mash1. In contrast, expression of Hes5 is restricted to clusters of neural progenitor cells and requires Mash1 function. Mutations in Hes1 and Hes5 also have distinct consequences on olfactory placode neurogenesis. Loss of Hes1 function leads both to expression of Mash1 outside of the normal domain of neurogenesis and to increased density of MASH1-positive progenitors within this domain, and results in an excess of neurons after a delay. A mutation in Hes5 does not produce any apparent defect. However, olfactory placodes that are double mutant for Hes1 and Hes5 upregulate Ngn1, a neural bHLH gene activated downstream of Mash1, and show a strong and rapid increase in neuronal density. Together, our results suggest that Hes1 regulates Mash1 transcription in the olfactory placode in two different contexts, initially as a prepattern gene defining the placodal domain undergoing neurogenesis and, subsequently, as a neurogenic gene controlling the density of neural progenitors in this domain. Hes5 synergizes with Hes1 and regulates neurogenesis at the level of Ngn1 expression. Therefore, the olfactory sensory neuron lineage is regulated at several steps by negative signals acting through different Hes genes and targeting the expression of different proneural gene homologs.
我们以小鼠胚胎中嗅基板的发育为模型,对bHLH转录抑制因子HES1和HES5在神经发生中的功能进行了表征。Hes1和Hes5在嗅基板中以不同模式表达,并受到不同的调控机制。Hes1在广泛的基板区域表达,在缺乏神经决定基因Mash1的情况下仍能维持。相反,Hes5的表达局限于神经祖细胞簇,并且需要Mash1的功能。Hes1和Hes5的突变对嗅基板神经发生也有不同的影响。Hes1功能的丧失导致Mash1在正常神经发生区域之外表达,并导致该区域内MASH1阳性祖细胞密度增加,且在延迟后导致神经元数量过多。Hes5的突变不会产生任何明显缺陷。然而,Hes1和Hes5双突变的嗅基板会上调Ngn1(一种在Mash1下游被激活的神经bHLH基因),并显示神经元密度强烈且迅速增加。总之,我们的结果表明,Hes1在两种不同情况下调节嗅基板中的Mash1转录,最初作为一个预模式基因定义正在进行神经发生的基板区域,随后作为一个神经发生基因控制该区域神经祖细胞的密度。Hes5与Hes1协同作用,并在Ngn1表达水平调节神经发生。因此,嗅觉感觉神经元谱系在多个步骤中受到通过不同Hes基因起作用并靶向不同神经源性基因同源物表达的负信号调控。