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J Cell Biol. 2013 Aug 19;202(4):667-83. doi: 10.1083/jcb.201301072.
2
Presynaptic calcium influx controls neurotransmitter release in part by regulating the effective size of the readily releasable pool.突触前钙离子内流通过调节易释放池的有效大小来控制神经递质的释放。
J Neurosci. 2013 Mar 13;33(11):4625-33. doi: 10.1523/JNEUROSCI.4031-12.2013.
3
RIM promotes calcium channel accumulation at active zones of the Drosophila neuromuscular junction.RIM 促进了果蝇神经肌肉接点活性区钙离子通道的聚集。
J Neurosci. 2012 Nov 21;32(47):16586-96. doi: 10.1523/JNEUROSCI.0965-12.2012.
4
Interaction of voltage-gated sodium channel Nav1.6 (SCN8A) with microtubule-associated protein Map1b.电压门控钠离子通道 Nav1.6(SCN8A)与微管相关蛋白 Map1b 的相互作用。
J Biol Chem. 2012 May 25;287(22):18459-66. doi: 10.1074/jbc.M111.336024. Epub 2012 Apr 3.
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SAF-A forms a complex with BRG1 and both components are required for RNA polymerase II mediated transcription.SAF-A 与 BRG1 形成复合物,这两个组件都是 RNA 聚合酶 II 介导的转录所必需的。
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Cancer Res. 2011 Dec 15;71(24):7537-46. doi: 10.1158/0008-5472.CAN-11-2170. Epub 2011 Oct 28.
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Microtubule-associated protein 1B (MAP1B) is required for dendritic spine development and synaptic maturation.微管相关蛋白 1B(MAP1B)对于树突棘发育和突触成熟是必需的。
J Biol Chem. 2011 Nov 25;286(47):40638-48. doi: 10.1074/jbc.M111.271320. Epub 2011 Oct 7.
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10
MAP1B binds to the NMDA receptor subunit NR3A and affects NR3A protein concentrations.MAP1B 与 NMDA 受体亚基 NR3A 结合,并影响 NR3A 蛋白浓度。
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微管相关蛋白 1/Futsch 在果蝇中的突触前作用:调节活性区数量和神经递质释放。

A presynaptic role of microtubule-associated protein 1/Futsch in Drosophila: regulation of active zone number and neurotransmitter release.

机构信息

Institut de Génomique Fonctionnelle, CNRS-UMR5203, INSERM-U661, Université Montpellier, Montpellier, Cedex 5, F-34094, France.

Institut de Génomique Fonctionnelle, CNRS-UMR5203, INSERM-U661, Université Montpellier, Montpellier, Cedex 5, F-34094, France

出版信息

J Neurosci. 2014 May 14;34(20):6759-71. doi: 10.1523/JNEUROSCI.4282-13.2014.

DOI:10.1523/JNEUROSCI.4282-13.2014
PMID:24828631
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6608111/
Abstract

Structural microtubule-associated proteins (MAPs), like MAP1, not only control the stability of microtubules, but also interact with postsynaptic proteins in the nervous system. Their presynaptic role has barely been studied. To tackle this question, we used the Drosophila model in which there is only one MAP1 homolog: Futsch, which is expressed at the larval neuromuscular junction, presynaptically only. We show that Futsch regulates neurotransmitter release and active zone density. Importantly, we provide evidence that this role of Futsch is not just the consequence of its microtubule-stabilizing function. Using high-resolution microscopy, we show that Futsch and microtubules are almost systematically present in close proximity to active zones, with Futsch being localized in-between microtubules and active zones. Using proximity ligation assays, we further demonstrate the proximity of Futsch, but not microtubules, to active zone components. Altogether our data are in favor of a model by which Futsch locally stabilizes active zones, by reinforcing their link with the underlying microtubule cytoskeleton.

摘要

结构微管相关蛋白(MAPs),如 MAP1,不仅控制微管的稳定性,还与神经系统中的突触后蛋白相互作用。它们在突触前的作用几乎没有被研究过。为了解决这个问题,我们使用了果蝇模型,其中只有一个 MAP1 同源物:Futsch,它在幼虫的神经肌肉接头处表达,仅在突触前表达。我们表明 Futsch 调节神经递质的释放和活性区密度。重要的是,我们提供了证据表明,Futsch 的这种作用不仅仅是其微管稳定功能的结果。使用高分辨率显微镜,我们表明 Futsch 和微管几乎总是与活性区紧密相邻,Futsch 位于微管和活性区之间。通过邻近连接测定,我们进一步证明了 Futsch 而不是微管与活性区成分接近。总的来说,我们的数据支持这样一种模型,即 Futsch 通过加强与基础微管细胞骨架的连接,局部稳定活性区。