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γ-微管蛋白独立于高尔基体前哨控制神经元微管极性。

Γ-tubulin controls neuronal microtubule polarity independently of Golgi outposts.

作者信息

Nguyen Michelle M, McCracken Christie J, Milner E S, Goetschius Daniel J, Weiner Alexis T, Long Melissa K, Michael Nick L, Munro Sean, Rolls Melissa M

机构信息

Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802.

Division of Cell Biology, MRC Laboratory of Molecular Biology, Cambridge CB2 0QH, United Kingdom.

出版信息

Mol Biol Cell. 2014 Jul 1;25(13):2039-50. doi: 10.1091/mbc.E13-09-0515. Epub 2014 May 7.

DOI:10.1091/mbc.E13-09-0515
PMID:24807906
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4072577/
Abstract

Neurons have highly polarized arrangements of microtubules, but it is incompletely understood how microtubule polarity is controlled in either axons or dendrites. To explore whether microtubule nucleation by γ-tubulin might contribute to polarity, we analyzed neuronal microtubules in Drosophila containing gain- or loss-of-function alleles of γ-tubulin. Both increased and decreased activity of γ-tubulin, the core microtubule nucleation protein, altered microtubule polarity in axons and dendrites, suggesting a close link between regulation of nucleation and polarity. To test whether nucleation might locally regulate polarity in axons and dendrites, we examined the distribution of γ-tubulin. Consistent with local nucleation, tagged and endogenous γ-tubulins were found in specific positions in dendrites and axons. Because the Golgi complex can house nucleation sites, we explored whether microtubule nucleation might occur at dendritic Golgi outposts. However, distinct Golgi outposts were not present in all dendrites that required regulated nucleation for polarity. Moreover, when we dragged the Golgi out of dendrites with an activated kinesin, γ-tubulin remained in dendrites. We conclude that regulated microtubule nucleation controls neuronal microtubule polarity but that the Golgi complex is not directly involved in housing nucleation sites.

摘要

神经元具有高度极化的微管排列方式,但人们对轴突或树突中微管极性是如何被控制的还不完全清楚。为了探究由γ-微管蛋白介导的微管成核是否有助于极性形成,我们分析了果蝇中含有γ-微管蛋白功能获得或功能缺失等位基因的神经元微管。微管成核的核心蛋白γ-微管蛋白的活性增加和降低,都会改变轴突和树突中的微管极性,这表明成核调节与极性之间存在紧密联系。为了测试成核是否可能在局部调节轴突和树突中的极性,我们检测了γ-微管蛋白的分布。与局部成核一致,在树突和轴突的特定位置发现了标记的和内源性的γ-微管蛋白。由于高尔基体复合物可以容纳成核位点,我们探究了微管成核是否可能发生在树突状高尔基体驻点。然而,并非所有需要通过调节成核来实现极性的树突中都存在明显的高尔基体驻点。此外,当我们用激活的驱动蛋白将高尔基体拖出树突时,γ-微管蛋白仍留在树突中。我们得出结论,受调控的微管成核控制着神经元微管的极性,但高尔基体复合物并不直接参与容纳成核位点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a14b/4072577/d08dbbe7664e/2039fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a14b/4072577/b259ab7e31fd/2039fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a14b/4072577/417373c3f97e/2039fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a14b/4072577/9b0cc0a3cc94/2039fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a14b/4072577/bc40e0d301ef/2039fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a14b/4072577/f1ddde22e92c/2039fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a14b/4072577/28f32e5436f9/2039fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a14b/4072577/40c03d22e571/2039fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a14b/4072577/d08dbbe7664e/2039fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a14b/4072577/b259ab7e31fd/2039fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a14b/4072577/417373c3f97e/2039fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a14b/4072577/9b0cc0a3cc94/2039fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a14b/4072577/bc40e0d301ef/2039fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a14b/4072577/f1ddde22e92c/2039fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a14b/4072577/28f32e5436f9/2039fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a14b/4072577/40c03d22e571/2039fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a14b/4072577/d08dbbe7664e/2039fig8.jpg

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