Johnson C D, Rand J B, Herman R K, Stern B D, Russell R L
Department of Zoology, University of Wisconsin, Madison 53706.
Neuron. 1988 Apr;1(2):165-73. doi: 10.1016/0896-6273(88)90201-2.
In C. elegans, the newly identified ace-3 is the third gene affecting acetylcholinesterase (AChE) activity. ace-3 II specifically affects class C AChE and is unlinked to ace-1 X or ace-2 I, which affect the other two AChE classes (A and B, respectively). Strains homozygous for an ace-3 mutation have no apparent behavioral or developmental defect; ace-1 ace-3 and ace-2 ace-3 double mutants are also nearly wild type. In contrast, ace-1 ace-2 ace-3 triple mutant animals are paralyzed and developmentally arrested; their embryonic development is relatively unimpaired, but they are unable to grow beyond the hatching stage. Based on the analysis of genetic mosaics, we conclude that in the absence of ace-2 and ace-3 function, the expression of ace-1(+) in muscle cells, but not in neurons, is essential for postembryonic viability.
在秀丽隐杆线虫中,新鉴定出的ace-3是影响乙酰胆碱酯酶(AChE)活性的第三个基因。ace-3 II特异性影响C类乙酰胆碱酯酶,且与影响其他两类乙酰胆碱酯酶(分别为A类和B类)的ace-1 X或ace-2 I不连锁。ace-3突变纯合子菌株没有明显的行为或发育缺陷;ace-1 ace-3和ace-2 ace-3双突变体也近乎野生型。相比之下,ace-1 ace-2 ace-3三突变动物会出现麻痹并在发育上停滞;它们的胚胎发育相对未受损害,但无法在孵化阶段之后生长。基于基因嵌合体分析,我们得出结论,在缺乏ace-2和ace-3功能的情况下,ace-1(+)在肌肉细胞而非神经元中的表达对于胚胎后期的生存能力至关重要。