Vactor D V, Sink H, Fambrough D, Tsoo R, Goodman C S
Howard Hughes Medical Institute, Department of Molecular and Cell Biology, University of California, Berkeley 94720.
Cell. 1993 Jun 18;73(6):1137-53. doi: 10.1016/0092-8674(93)90643-5.
In each abdominal hemisegment of the Drosophila embryo, an array of 30 muscle fibers is innervated by about 34 motoneurons in a highly stereotyped and cell-specific fashion. To begin to elucidate the molecular basis of neural specificity in this system, we conducted a genetic screen for mutations affecting neuromuscular connectivity. We focus on 5 genes required for specific aspects of pathway (beaten path, stranded, and short stop) and target (walkabout and clueless) recognition. The different classes of mutant phenotypes suggest that neural specificity is controlled by a hierarchy of molecular mechanisms: motoneurons are guided toward the correct region of mesoderm, in many cases navigating a series of choice points along the way; they then display an affinity for a particular domain of neighboring muscles; and finally, they recognize their specific muscle target from within this domain.
在果蝇胚胎的每个腹部半节段中,一组30根肌肉纤维以高度刻板且细胞特异性的方式由约34个运动神经元支配。为了开始阐明该系统中神经特异性的分子基础,我们针对影响神经肌肉连接性的突变进行了遗传筛选。我们聚焦于通路(循经、搁浅和短停)和靶标(漫游和无知)识别特定方面所需的5个基因。不同类别的突变体表型表明,神经特异性受分子机制层次结构的控制:运动神经元被引导至中胚层的正确区域,在许多情况下会沿途经过一系列选择点;然后它们对相邻肌肉的特定区域表现出亲和力;最后,它们从该区域内识别出其特定的肌肉靶标。