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Tao 在果蝇的神经肌肉接头发育过程中负调控 BMP 信号通路。

Tao Negatively Regulates BMP Signaling During Neuromuscular Junction Development in Drosophila.

机构信息

Department of Biology, John Carroll University, University Heights, Ohio, 44118.

Molecular Genetics and Cell Biology, University of Chicago, Chicago, Illinois, 60637.

出版信息

Dev Neurobiol. 2019 Apr;79(4):335-349. doi: 10.1002/dneu.22681. Epub 2019 May 11.

DOI:10.1002/dneu.22681
PMID:31002474
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6848449/
Abstract

The coordinated growth and development of synapses is critical for all aspects of neural circuit function and mutations that disrupt these processes can result in various neurological defects. Several anterograde and retrograde signaling pathways, including the canonical Bone Morphogenic Protein (BMP) pathway, regulate synaptic development in vertebrates and invertebrates. At the Drosophila larval neuromuscular junction (NMJ), the retrograde BMP pathway is a part of the machinery that controls NMJ expansion concurrent with larval growth. We sought to determine whether the conserved Hippo pathway, critical for proportional growth in other tissues, also functions in NMJ development. We found that neuronal loss of the serine-threonine protein kinase Tao, a regulator of the Hippo signaling pathway, results in supernumerary boutons which contain a normal density of active zones. Tao is also required for proper synaptic function, as reduction of Tao results in NMJs with decreased evoked excitatory junctional potentials. Surprisingly, Tao function in NMJ growth is independent of the Hippo pathway. Instead, our experiments suggest that Tao negatively regulates BMP signaling as reduction of Tao leads to an increase in pMad levels in motor neuron nuclei and an increase in BMP target gene expression. Taken together, these results support a role for Tao as a novel inhibitor of BMP signaling in motor neurons during synaptic development and function.

摘要

突触的协调生长和发育对于神经回路功能的各个方面都至关重要,而破坏这些过程的突变可能导致各种神经缺陷。几种顺行和逆行信号通路,包括经典的骨形态发生蛋白(BMP)通路,调节脊椎动物和无脊椎动物的突触发育。在果蝇幼虫的神经肌肉接点(NMJ)中,逆行 BMP 通路是控制 NMJ 与幼虫生长同时扩张的机制的一部分。我们试图确定保守的 Hippo 通路是否也在 NMJ 发育中起作用,Hippo 通路对于其他组织中的比例生长至关重要。我们发现,丝氨酸-苏氨酸蛋白激酶 Tao 的神经元缺失,Hippo 信号通路的调节剂,导致含有正常活性区密度的多余突触及。Tao 对于正常的突触功能也是必需的,因为 Tao 的减少导致 NMJ 中的诱发兴奋性连接电位降低。令人惊讶的是,Tao 在 NMJ 生长中的功能独立于 Hippo 通路。相反,我们的实验表明,Tao 负调控 BMP 信号,因为 Tao 的减少导致运动神经元核中 pMad 水平的增加和 BMP 靶基因表达的增加。总之,这些结果支持 Tao 作为在突触发育和功能过程中运动神经元中 BMP 信号的新型抑制剂的作用。

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本文引用的文献

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A Hippo-like Signaling Pathway Controls Tracheal Morphogenesis in Drosophila melanogaster.Hippo 样信号通路控制果蝇的气管形态发生。
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Yorkie Functions at the Cell Cortex to Promote Myosin Activation in a Non-transcriptional Manner.约克犬在细胞皮层发挥作用,以非转录方式促进肌球蛋白的激活。
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Mammalian Sterile20-like Kinases: Signalings and Roles in Central Nervous System.
神经发育障碍中TAO激酶家族的临床和神经生物学方面
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Target-dependent retrograde signaling mediates synaptic plasticity at the Drosophila neuromuscular junction.靶向依赖性逆行信号介导果蝇神经肌肉接点的突触可塑性。
Dev Neurobiol. 2019 Nov;79(11-12):895-912. doi: 10.1002/dneu.22731. Epub 2020 Feb 11.
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A new TAO kinase inhibitor reduces tau phosphorylation at sites associated with neurodegeneration in human tauopathies.一种新型 TAO 激酶抑制剂可减少与神经退行性变相关的人 tau 病中 tau 磷酸化位点的磷酸化。
Acta Neuropathol Commun. 2018 May 7;6(1):37. doi: 10.1186/s40478-018-0539-8.
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Kinesin Khc-73/KIF13B modulates retrograde BMP signaling by influencing endosomal dynamics at the Drosophila neuromuscular junction.驱动蛋白 Khc-73/KIF13B 通过影响果蝇神经肌肉接头处的内体动力学来调节逆行 BMP 信号。
PLoS Genet. 2018 Jan 26;14(1):e1007184. doi: 10.1371/journal.pgen.1007184. eCollection 2018 Jan.
6
Input-Specific Plasticity and Homeostasis at the Drosophila Larval Neuromuscular Junction.果蝇幼虫神经肌肉接头处的输入特异性可塑性与稳态
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