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Tuba8 通过调节微管蛋白 C 末端的修饰来驱动皮质放射状胶质向顶端中间祖细胞分化。

Tuba8 Drives Differentiation of Cortical Radial Glia into Apical Intermediate Progenitors by Tuning Modifications of Tubulin C Termini.

机构信息

Centre for Developmental Neurobiology, King's College London, New Hunt's House, Guy's Campus, London SE1 1UL, UK.

Department of Otolaryngology-Head and Neck Surgery, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

出版信息

Dev Cell. 2020 Feb 24;52(4):477-491.e8. doi: 10.1016/j.devcel.2020.01.036.

Abstract

Most adult neurons and glia originate from radial glial progenitors (RGs), a type of stem cell typically extending from the apical to the basal side of the developing cortex. Precise regulation of the choice between RG self-renewal and differentiation is critical for normal development, but the mechanisms underlying this transition remain elusive. We show that the non-canonical tubulin Tuba8, transiently expressed in cortical progenitors, drives differentiation of RGs into apical intermediate progenitors, a more restricted progenitor type lacking attachment to the basal lamina. This effect depends on the unique C-terminal sequence of Tuba8 that antagonizes tubulin tyrosination and Δ2 cleavage, two post-translational modifications (PTMs) essential for RG fiber maintenance and the switch between direct and indirect neurogenesis and ultimately distinct neuronal lineage outcomes. Our work uncovers an instructive role of a developmentally regulated tubulin isotype in progenitor differentiation and provides new insights into biological functions of the cellular tubulin PTM "code."

摘要

大多数成年神经元和神经胶质细胞起源于放射状胶质祖细胞(RG),这是一种干细胞,通常从发育中的皮层的顶端延伸到底部。RG 自我更新和分化之间的选择的精确调控对于正常发育至关重要,但这种转变的机制仍不清楚。我们发现,非典型微管蛋白 Tuba8 在皮质祖细胞中短暂表达,驱动 RG 分化为顶端中间祖细胞,这是一种更局限的祖细胞类型,缺乏与基底膜的附着。这种效应取决于 Tuba8 的独特 C 末端序列,该序列拮抗微管蛋白酪氨酸化和 Δ2 切割,这两种翻译后修饰(PTM)对于 RG 纤维的维持以及直接和间接神经发生之间的转换以及最终不同的神经元谱系结果至关重要。我们的工作揭示了发育调节的微管蛋白同工型在祖细胞分化中的指导作用,并为细胞微管蛋白 PTM“密码”的生物学功能提供了新的见解。

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