Petrovich T Z, Merakovsky J, Kelly L E
Department of Genetics, University of Melbourne, Parkville, Victoria, Australia.
Genetics. 1993 Apr;133(4):955-65. doi: 10.1093/genetics/133.4.955.
The genetic complementation patterns of both behavioral and lethal alleles at the stoned locus have been characterized. Mosaic analysis of a stoned lethal allele suggests that stoned functions either in the nervous system or in both the nervous system and musculature, but is not required for gross neural development. The behavioral alleles stnts and stnC, appear to be defective in a diametrically opposite sense, show interallelic complementation, and indicate distinct roles for the stoned gene product in the visual system and in motor coordination. A number of other neurological mutations have been investigated for their possible interaction with the viable stoned alleles. Mutations at two loci, dunce and shibire, act synergistically with the stnts mutations to cause lethality, but fail to interact with stnC. A third variant (Suppressor of stoned) has been identified which can suppress the debilitation associated with the stnts mutations. These data, together with a previously identified interaction between the stnts and tan mutants, indicate a central role for the stoned gene product in neuronal function, and suggests that the stoned gene product interacts, either directly or indirectly, with the neural cAMP second messenger system, with the synaptic membrane recycling pathway via dynamin, and with biogenic amine metabolism.
已对“stoned”位点的行为和致死等位基因的遗传互补模式进行了表征。对一个“stoned”致死等位基因的嵌合体分析表明,“stoned”要么在神经系统中起作用,要么在神经系统和肌肉组织中都起作用,但对于整体神经发育并非必需。行为等位基因“stnts”和“stnC”,似乎在完全相反的意义上存在缺陷,表现出等位基因间互补,并表明“stoned”基因产物在视觉系统和运动协调中具有不同作用。已经研究了许多其他神经学突变与存活的“stoned”等位基因可能存在的相互作用。两个位点“dunce”和“shibire”的突变与“stnts”突变协同作用导致致死,但与“stnC”不发生相互作用。已鉴定出第三个变体(“stoned”的抑制子),它可以抑制与“stnts”突变相关的衰弱。这些数据,连同先前鉴定出的“stnts”和“tan”突变体之间的相互作用,表明“stoned”基因产物在神经元功能中起核心作用,并表明“stoned”基因产物直接或间接与神经cAMP第二信使系统、通过发动蛋白的突触膜回收途径以及生物胺代谢相互作用。