Key Lab of Organ Development and Regeneration of Zhejiang Province, College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, Zhejiang 310036, China; The Dorris Neuroscience Center, Department of Molecular and Cellular Neuroscience, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
The Dorris Neuroscience Center, Department of Molecular and Cellular Neuroscience, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA; Kellogg School of Science and Technology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Cell Rep. 2014 Feb 27;6(4):737-47. doi: 10.1016/j.celrep.2014.01.024. Epub 2014 Feb 13.
Neural plasticity requires protein synthesis, but the identity of newly synthesized proteins generated in response to plasticity-inducing stimuli remains unclear. We used in vivo bio-orthogonal noncanonical amino acid tagging (BONCAT) with the methionine analog azidohomoalanine (AHA) combined with the multidimensional protein identification technique (MudPIT) to identify proteins that are synthesized in the tadpole brain over 24 hr. We induced conditioning-dependent plasticity of visual avoidance behavior, which required N-methyl-D-aspartate (NMDA) and Ca(2+)-permeable α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors, αCaMKII, and rapid protein synthesis. Combining BONCAT with western blots revealed that proteins including αCaMKII, MEK1, CPEB, and GAD65 are synthesized during conditioning. Acute synthesis of CPEB during conditioning is required for behavioral plasticity as well as conditioning-induced synaptic and structural plasticity in the tectal circuit. We outline a signaling pathway that regulates protein-synthesis-dependent behavioral plasticity in intact animals, identify newly synthesized proteins induced by visual experience, and demonstrate a requirement for acute synthesis of CPEB in plasticity.
神经可塑性需要蛋白质合成,但对于响应可塑性诱导刺激产生的新合成蛋白质的身份仍不清楚。我们使用体内生物正交非典型氨基酸标记(BONCAT)与甲硫氨酸类似物叠氮高丙氨酸(AHA)结合多维蛋白质鉴定技术(MudPIT)来鉴定在 24 小时内合成的在蝌蚪大脑中的蛋白质。我们诱导了视觉回避行为的条件依赖性可塑性,这需要 N-甲基-D-天冬氨酸(NMDA)和 Ca(2+)可渗透的 α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体、αCaMKII 和快速蛋白质合成。BONCAT 与蛋白质印迹的结合表明,包括 αCaMKII、MEK1、CPEB 和 GAD65 在内的蛋白质在条件作用过程中被合成。在条件作用过程中 CPEB 的急性合成对于行为可塑性以及顶盖电路中的诱导性突触和结构可塑性都是必需的。我们概述了一条信号通路,该通路调节完整动物中的蛋白质合成依赖性行为可塑性,鉴定由视觉经验诱导的新合成蛋白质,并证明 CPEB 的急性合成在可塑性中是必需的。