Groupe de Recherche en Neurosciences, Département de Chimie-Biologie, Université du Québec à Trois-Rivières, Trois-Rivières, Québec, Canada.
Behav Brain Res. 2011 Aug 1;221(1):108-17. doi: 10.1016/j.bbr.2011.02.030. Epub 2011 Mar 2.
Much research has implicated the striatum in motor learning, but the underlying mechanism is still under extensive investigation. In this study, genome-wide analysis of gene expression was conducted in mice that have learned a complex motor task. It is well recognized that successful learning requires repetitive training and is learned slowly over several training sessions. We therefore used mice that have fully learned the accelerating rotarod task that discriminates the faster and slower phases of motor learning. As important modulators of movement behavior, the striatum was the target of this analysis along with the cerebellum and anterior cortex. To identify potential genes implicated in long memorization process, we compared the lists of genes modulated in the striatum to those modulated in the cerebellum and cortex. As a second approach, we also determined which gene ontology categories were enriched in modulated striatal genes and identified genes with the highest numbers of annotation throughout categories. Although only some of these changes were further confirmed by RT-PCR, these two complementary analyses allowed the identification of highly relevant genes like calcium/calmodulin-dependent protein kinase 2, protein kinase C zeta and N-methyl-D-aspartate receptors. Notably, these genes are all associated with synaptic plasticity, suggesting that stabilized neuronal connections in the striatum are the foundation of durable motor memory. Our study provides the first report of a whole genome analysis of gene expression in mice that have memorized a new complex motor task, and expands our knowledge on striatal gene expression changes associated with motor skill learning.
大量研究表明纹状体在运动学习中起作用,但潜在的机制仍在广泛研究中。在这项研究中,对已经学习了复杂运动任务的小鼠进行了全基因组基因表达分析。众所周知,成功的学习需要重复训练,并且需要在几个训练过程中缓慢学习。因此,我们使用已经完全学会加速旋转棒任务的小鼠,该任务可以区分运动学习的较快和较慢阶段。作为运动行为的重要调节剂,纹状体与小脑和前皮质一起成为该分析的目标。为了确定可能与长期记忆过程有关的潜在基因,我们将纹状体中调节的基因列表与小脑和皮质中调节的基因列表进行了比较。作为第二种方法,我们还确定了哪些基因本体论类别在调节的纹状体基因中富集,并确定了在整个类别中具有最高注释数量的基因。尽管其中一些变化仅通过 RT-PCR 进一步证实,但这两种互补分析允许鉴定出高度相关的基因,如钙/钙调蛋白依赖性蛋白激酶 2、蛋白激酶 C zeta 和 N-甲基-D-天冬氨酸受体。值得注意的是,这些基因都与突触可塑性有关,这表明纹状体中稳定的神经元连接是持久运动记忆的基础。我们的研究首次报道了对已经记住新的复杂运动任务的小鼠进行全基因组基因表达分析,并扩展了我们对与运动技能学习相关的纹状体基因表达变化的认识。