Jiménez F, Martin-Morris L E, Velasco L, Chu H, Sierra J, Rosen D R, White K
Centro de Biología Molecular Severo Ochoa, Universidad Autónoma, CSIC, Madrid, Spain.
EMBO J. 1995 Jul 17;14(14):3487-95. doi: 10.1002/j.1460-2075.1995.tb07355.x.
The development of the central nervous system in Drosophila is initiated by the segregation of neuroblasts, the neural progenitors, from the embryonic neuroectoderm. This process is guided by at least two classes of genes: the achaete-scute complex (AS-C) proneural genes and the neurogenic genes. It has been known for some time that loss-of-function mutations in the AS-C result in neural hypoplasia and the first observed defect is failure of segregation of a fraction of neuroblasts. Loss-of-function mutations at the ventral nervous system defective (vnd) locus are known to lead to similar phenotypic defects in early neurogenesis. More recently, the vnd locus has been implicated in the regulation of the proneural AS-C genes and the neurogenic genes of the Enhancer of split complex. In this paper we report the identification of a transcript associated with the vnd locus, the transcript distribution in embryogenesis, which is compatible with the nervous system mutant phenotypes described for this gene, and that the protein product is a member of the NK-2 homeodomain family. We discuss these findings within the framework of early Drosophila neurogenesis and the known phenotypes associated with the vnd locus.
果蝇中枢神经系统的发育始于神经母细胞(即神经祖细胞)从胚胎神经外胚层的分离。这一过程至少受两类基因的引导:achaete-scute复合体(AS-C)原神经基因和神经源基因。一段时间以来人们已经知道,AS-C功能丧失性突变会导致神经发育不全,首次观察到的缺陷是一部分神经母细胞分离失败。已知腹侧神经系统缺陷(vnd)位点的功能丧失性突变会在早期神经发生中导致类似的表型缺陷。最近,vnd位点与原神经AS-C基因和分裂增强子复合体的神经源基因的调控有关。在本文中,我们报告了与vnd位点相关的一种转录物的鉴定、其在胚胎发生中的转录物分布,这与该基因所描述的神经系统突变体表型相符,并且该蛋白质产物是NK-2同源域家族的成员。我们在果蝇早期神经发生的框架以及与vnd位点相关的已知表型内讨论这些发现。