Orgad S., Llamazares S., Dudai Y., Ferrús A.
Neurobiology Department, The Weizmann Institute for Science, Rehovot, Israel.
Eur J Neurosci. 1989 Jul;1(4):367-373. doi: 10.1111/j.1460-9568.1989.tb00801.x.
The tetanic (tta; X.-52.6) mutation has been isolated on the basis of its sensitivity to extradoses of the normal Shaker gene complex (ShC) where the K+ channel la is encoded. The mutant shows up to threefold elevation of the membrane bound protein phosphatase type 1 (PP1) activity in body extracts, probably due to reduced levels of the PP1 specific inhibitor 2 (I-2). By contrast, PP1 activity in the head is only half of the normal value. In addition, tta fails to perform normally in a negative reinforcement olfactory paradigm. The functional relationships between phosphorylation, K+ currents, phosphatase activity and modulation of synaptic activity during learning and memory are discussed in the light of their possible genetic links.
强直性(tta;X.-52.6)突变是根据其对正常的“震荡器”基因复合体(ShC,其中编码K+通道la)额外剂量的敏感性而分离出来的。该突变体在身体提取物中膜结合蛋白磷酸酶1(PP1)活性高达正常水平的三倍,这可能是由于PP1特异性抑制剂2(I-2)水平降低所致。相比之下,头部的PP1活性仅为正常值的一半。此外,tta在负强化嗅觉范式中不能正常发挥作用。根据它们可能的遗传联系,讨论了学习和记忆过程中磷酸化、K+电流、磷酸酶活性与突触活动调节之间的功能关系。