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p27 通过调节 α-微管蛋白乙酰转移酶 1 的稳定性来调节轴突运输。

p27 Modulates Axonal Transport by Regulating α-Tubulin Acetyltransferase 1 Stability.

机构信息

Liege Université, GIGA-Neurosciences, Interdisciplinary Cluster for Applied Genoproteomics (GIGA-R), 4000 Liège, Belgium; Universiteit Hasselt, BIOMED, 3500 Hasselt, Belgium.

Laboratory for Neurodegenerative Diseases and Personalized Medicine, Department of Cell Research and Immunology, The George S. Wise Faculty for Life Sciences, Sagol School of Neurosciences, Tel Aviv University, Ramat Aviv, 69978 Tel Aviv, Israel.

出版信息

Cell Rep. 2018 May 22;23(8):2429-2442. doi: 10.1016/j.celrep.2018.04.083.

Abstract

The protein p27 plays roles that extend beyond cell-cycle regulation during cerebral cortex development, such as the regulation of neuronal migration and neurite branching via signaling pathways that converge on the actin and microtubule cytoskeletons. Microtubule-dependent transport is essential for the maturation of neurons and the establishment of neuronal connectivity though synapse formation and maintenance. Here, we show that p27 controls the transport of vesicles and organelles along the axon of mice cortical projection neurons in vitro. Moreover, suppression of the p27 ortholog, dacapo, in Drosophila melanogaster disrupts axonal transport in vivo, leading to the reduction of locomotor activity in third instar larvae and adult flies. At the molecular level, p27 stabilizes the α-tubulin acetyltransferase 1, thereby promoting the acetylation of microtubules, a post-translational modification required for proper axonal transport.

摘要

蛋白 p27 在大脑皮层发育过程中的细胞周期调控之外发挥作用,例如通过信号通路调节神经元迁移和神经突分支,这些信号通路汇聚到肌动蛋白和微管细胞骨架上。微管依赖性运输对于神经元的成熟和通过突触形成和维持建立神经元连接至关重要。在这里,我们表明 p27 控制着体外培养的小鼠皮质投射神经元轴突中囊泡和细胞器的运输。此外,在果蝇中抑制 p27 的同源物 dacapo 会破坏体内的轴突运输,导致三龄幼虫和成年果蝇的运动活性降低。在分子水平上,p27 稳定了 α-微管乙酰转移酶 1,从而促进微管的乙酰化,这是适当的轴突运输所必需的翻译后修饰。

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