Guillemot F
Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS, INSERM, Université Louis Pasteur, Collège de France, Illkirch, France.
Biol Cell. 1995;84(1-2):3-6. doi: 10.1016/0248-4900(96)81312-8.
The development of neural lineages is a complex process which is being actively investigated in both vertebrate and invertebrate models. A detailed genetic analysis of sensory organ development in Drosophila has revealed the contribution of numerous genes which function to progressively to specify the fate of neural precursor cells. Many of these genes have mammalian homologs which are also expressed in the developing nervous system, among which two families of genes encoding transcription factors of the helix-loop-helix class. The two mouse Mash genes are homologs of the Drosophila achaete-scute genes, which are positive regulators of neural precursor development. The five mouse HES genes are homologs of the Drosophila hairy and Enhancer of split genes, which act as negative regulators in this process. We have generated a null mutation in the mouse Mash1 gene by homologous recombination in embryonic stem cells. Animals homozygous for this mutation die at birth, and show severe losses in olfactory and autonomic neurons. In both lineages, the mutation appears to affect the development of neuronal precursors. We have also started a genetic analysis of the mouse HES genes to study their function during neurogenesis and the possibility that they regulate the activity of Mash1 and other positive regulators.
神经谱系的发育是一个复杂的过程,目前在脊椎动物和无脊椎动物模型中都在积极研究。对果蝇感觉器官发育的详细遗传分析揭示了众多基因的作用,这些基因逐步发挥功能来确定神经前体细胞的命运。其中许多基因在哺乳动物中有同源物,它们也在发育中的神经系统中表达,其中包括两个编码螺旋-环-螺旋类转录因子的基因家族。两个小鼠Mash基因是果蝇achaete-scute基因的同源物,后者是神经前体发育的正向调节因子。五个小鼠HES基因是果蝇hairy和split增强子基因的同源物,它们在此过程中作为负向调节因子起作用。我们通过胚胎干细胞中的同源重组在小鼠Mash1基因中产生了一个无效突变。该突变的纯合动物在出生时死亡,并在嗅觉和自主神经元中出现严重缺失。在这两个谱系中,该突变似乎影响神经元前体的发育。我们还开始了对小鼠HES基因的遗传分析,以研究它们在神经发生过程中的功能以及它们调节Mash1和其他正向调节因子活性的可能性。