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非典型肌球蛋白调节树突分支。

Atypical Myosin Tunes Dendrite Arbor Subdivision.

机构信息

Laboratory for Neurodiversity, RIKEN Center for Brain Science, Wako-shi, Saitama 351-0198, Japan.

Laboratory for Neurodiversity, RIKEN Center for Brain Science, Wako-shi, Saitama 351-0198, Japan; School of Health Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan 16150, Malaysia.

出版信息

Neuron. 2020 May 6;106(3):452-467.e8. doi: 10.1016/j.neuron.2020.02.002. Epub 2020 Mar 9.

Abstract

Dendrite arbor pattern determines the functional characteristics of a neuron. It is founded on primary branch structure, defined through cell intrinsic and transcription-factor-encoded mechanisms. Developing arbors have extensive acentrosomal microtubule dynamics, and here, we report an unexpected role for the atypical actin motor Myo6 in creating primary branch structure by specifying the position, polarity, and targeting of these events. We carried out in vivo time-lapse imaging of Drosophila adult sensory neuron differentiation, integrating machine-learning-based quantification of arbor patterning with molecular-level tracking of cytoskeletal remodeling. This revealed that Myo6 and the transcription factor Knot regulate transient surges of microtubule polymerization at dendrite tips; they drive retrograde extension of an actin filament array that specifies anterograde microtubule polymerization and guides these microtubules to subdivide the tip into multiple branches. Primary branches delineate functional compartments; this tunable branching mechanism is key to define and diversify dendrite arbor compartmentalization.

摘要

树突分支模式决定了神经元的功能特征。它建立在初级分支结构的基础上,通过细胞内在和转录因子编码机制来定义。发育中的树突具有广泛的无中心体微管动力学,在这里,我们报告了非典型肌球蛋白 6(Myo6)在通过指定这些事件的位置、极性和靶向来创建初级分支结构方面的意外作用。我们对果蝇成年感觉神经元分化进行了体内延时成像,将基于机器学习的树突模式定量分析与细胞骨架重塑的分子水平跟踪相结合。这表明,Myo6 和转录因子 Knot 调节树突末梢处微管聚合的短暂激增;它们驱动肌动蛋白丝阵列的逆行延伸,该延伸指定了顺行微管聚合,并指导这些微管将末梢细分成分叉的多个分支。初级分支描绘了功能区室;这种可调分枝机制是定义和多样化树突分支区室化的关键。

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