Liu Han-Hsuan, Cline Hollis T
Dorris Neuroscience Center, Kellogg School of Science and Technology, The Scripps Research Institute, La Jolla, California 92037.
Dorris Neuroscience Center, Kellogg School of Science and Technology, The Scripps Research Institute, La Jolla, California 92037
J Neurosci. 2016 Jul 6;36(27):7325-39. doi: 10.1523/JNEUROSCI.4282-15.2016.
Fragile X mental retardation protein (FMRP) is thought to regulate neuronal plasticity by limiting dendritic protein synthesis, but direct demonstration of a requirement for FMRP control of local protein synthesis during behavioral plasticity is lacking. Here we tested whether FMRP knockdown in Xenopus optic tectum affects local protein synthesis in vivo and whether FMRP knockdown affects protein synthesis-dependent visual avoidance behavioral plasticity. We tagged newly synthesized proteins by incorporation of the noncanonical amino acid azidohomoalanine and visualized them with fluorescent noncanonical amino acid tagging (FUNCAT). Visual conditioning and FMRP knockdown produce similar increases in FUNCAT in tectal neuropil. Induction of visual conditioning-dependent behavioral plasticity occurs normally in FMRP knockdown animals, but plasticity degrades over 24 h. These results indicate that FMRP affects visual conditioning-induced local protein synthesis and is required to maintain the visual conditioning-induced behavioral plasticity.
Fragile X syndrome (FXS) is the most common form of inherited intellectual disability. Exaggerated dendritic protein synthesis resulting from loss of fragile X mental retardation protein (FMRP) is thought to underlie cognitive deficits in FXS, but no direct evidence has demonstrated that FMRP-regulated dendritic protein synthesis affects behavioral plasticity in intact animals. Xenopus tadpoles exhibit a visual avoidance behavior that improves with visual conditioning in a protein synthesis-dependent manner. We showed that FMRP knockdown and visual conditioning dramatically increase protein synthesis in neuronal processes. Furthermore, induction of visual conditioning-dependent behavioral plasticity occurs normally after FMRP knockdown, but performance rapidly deteriorated in the absence of FMRP. These studies show that FMRP negatively regulates local protein synthesis and is required to maintain visual conditioning-induced behavioral plasticity in vivo.
脆性X智力低下蛋白(FMRP)被认为通过限制树突蛋白合成来调节神经元可塑性,但缺乏在行为可塑性过程中FMRP对局部蛋白合成控制的必要性的直接证据。在这里,我们测试了非洲爪蟾视顶盖中FMRP的敲低是否会影响体内局部蛋白合成,以及FMRP敲低是否会影响依赖蛋白合成的视觉回避行为可塑性。我们通过掺入非标准氨基酸叠氮高丙氨酸来标记新合成的蛋白质,并使用荧光非标准氨基酸标记(FUNCAT)对其进行可视化。视觉条件反射和FMRP敲低在顶盖神经纤维网中使FUNCAT产生类似的增加。依赖视觉条件反射的行为可塑性的诱导在FMRP敲低的动物中正常发生,但可塑性在24小时内会退化。这些结果表明,FMRP影响视觉条件反射诱导的局部蛋白合成,并且是维持视觉条件反射诱导的行为可塑性所必需的。
脆性X综合征(FXS)是遗传性智力残疾最常见的形式。由于脆性X智力低下蛋白(FMRP)缺失导致的过度树突蛋白合成被认为是FXS认知缺陷的基础,但没有直接证据表明FMRP调节的树突蛋白合成会影响完整动物的行为可塑性。非洲爪蟾蝌蚪表现出一种视觉回避行为,这种行为会随着视觉条件反射以依赖蛋白合成的方式得到改善。我们表明,FMRP敲低和视觉条件反射会显著增加神经元突起中的蛋白合成。此外,FMRP敲低后,依赖视觉条件反射的行为可塑性的诱导正常发生,但在没有FMRP的情况下,表现会迅速恶化。这些研究表明,FMRP对局部蛋白合成起负调节作用,并且是在体内维持视觉条件反射诱导的行为可塑性所必需的。