Atkinson N S, Brenner R, Chang W m, Wilbur J, Larimer J L, Yu J
Section of Neurobiology, School of Biological Sciences, Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, Texas 78712-1064, USA.
J Neurosci. 2000 Apr 15;20(8):2988-93. doi: 10.1523/JNEUROSCI.20-08-02988.2000.
The Drosophila slowpoke gene encodes a BK-type calcium-activated potassium channel. Null mutations in slowpoke perturb the signaling properties of neurons and muscles and cause behavioral defects. The animals fly very poorly compared with wild-type strains and, after exposure to a bright but cool light or a heat pulse, exhibit a "sticky-feet" phenotype. Expression of slowpoke arises from five transcriptional promoters that express the gene in neural, muscle, and epithelial tissues. A chromosomal deletion (ash2(18)) has been identified that removes the neuronal promoters but not the muscle-tracheal cell promoter. This deletion complements the flight defect of slowpoke null mutants but not the sticky-feet phenotype. Electrophysiological assays confirm that the ash2(18) chromosome restores normal electrical properties to the flight muscle. This suggests that the flight defect arises from a lack of slowpoke expression in muscle, whereas the sticky-feet phenotype arises from a lack of expression in nervous tissue.
果蝇慢poke基因编码一种BK型钙激活钾通道。慢poke基因的无效突变扰乱了神经元和肌肉的信号特性,并导致行为缺陷。与野生型菌株相比,这些动物飞行能力很差,在暴露于明亮但凉爽的光线或热脉冲后,表现出“粘脚”表型。慢poke基因的表达源自五个转录启动子,这些启动子在神经、肌肉和上皮组织中表达该基因。已鉴定出一种染色体缺失(ash2(18)),它去除了神经元启动子,但没有去除肌肉-气管细胞启动子。这种缺失弥补了慢poke无效突变体的飞行缺陷,但没有弥补“粘脚”表型。电生理分析证实,ash2(18)染色体恢复了飞行肌肉的正常电特性。这表明飞行缺陷是由于肌肉中缺乏慢poke基因的表达,而“粘脚”表型是由于神经组织中缺乏表达所致。