Mehren Jennifer E, Griffith Leslie C
Department of Biology and Volen Center for Complex Systems, Brandeis University, Waltham, Massachusetts 02454-9110, USA.
J Neurosci. 2004 Nov 24;24(47):10584-93. doi: 10.1523/JNEUROSCI.3560-04.2004.
Calcium/calmodulin-dependent protein kinase II (CaMKII) is abundant in the CNS and is crucial for cellular and behavioral plasticity. It is thought that the ability of CaMKII to autophosphorylate and become Ca2+ independent allows it to act as a molecular memory switch. We have shown previously that inhibition of Drosophila CaMKII leads to impaired performance in the courtship conditioning associative memory assay, but it was unknown whether the constitutive form of the kinase had a special role in learning. In this study, we use a tripartite transgenic system combining GAL4/UAS with the tetracycline-off system to spatially and temporally manipulate levels of Ca2+-independent CaMKII activity in Drosophila. We find an enhancement of information processing during the training period with Ca2+-independent, but not Ca2+-dependent, CaMKII. During training, control animals have a lag before active suppression of courtship begins. Animals expressing Ca2+-independent CaMKII have no lag, implying that there is a threshold level of Ca2+-independent activity that must be present to suppress courtship. This is the first demonstration, in any organism, of enhanced behavioral plasticity with overexpression of constitutively active CaMKII. Anatomical studies indicate that transgene expression in antennal lobes and extrinsic mushroom body neurons drives this behavioral enhancement. Interestingly, immediate memory was unaffected by expression of T287D CaMKII in mushroom bodies, although previous studies have shown that CaMKII activity is required in this brain region for memory formation. These results suggest that the biochemical mechanisms of CaMKII-dependent memory formation are threshold based in only a subset of neurons.
钙/钙调蛋白依赖性蛋白激酶II(CaMKII)在中枢神经系统中含量丰富,对细胞和行为可塑性至关重要。据认为,CaMKII的自身磷酸化能力以及变得不依赖Ca2+的特性使其能够充当分子记忆开关。我们之前已经表明,抑制果蝇CaMKII会导致求偶条件性联想记忆试验中的表现受损,但尚不清楚该激酶的组成型形式在学习中是否具有特殊作用。在本研究中,我们使用一种将GAL4/UAS与四环素关闭系统相结合的三方转基因系统,在空间和时间上操纵果蝇中不依赖Ca2+的CaMKII活性水平。我们发现,在训练期间,不依赖Ca2+而非依赖Ca2+的CaMKII会增强信息处理能力。在训练过程中,对照动物在主动抑制求偶开始之前会有一个延迟。表达不依赖Ca2+的CaMKII的动物没有延迟,这意味着必须存在一定阈值水平的不依赖Ca2+的活性才能抑制求偶。这是在任何生物体中首次证明组成型活性CaMKII过表达会增强行为可塑性。解剖学研究表明,触角叶和外在蘑菇体神经元中的转基因表达驱动了这种行为增强。有趣的是,尽管先前的研究表明该脑区的记忆形成需要CaMKII活性,但蘑菇体中T287D CaMKII的表达并未影响即时记忆。这些结果表明,依赖CaMKII的记忆形成的生化机制仅在一部分神经元中基于阈值。