Suppr超能文献

RIMB-1/RIM 结合蛋白和 UNC-10/RIM 冗余调节电压门控钙通道在. 的突触前定位。

RIMB-1/RIM-Binding Protein and UNC-10/RIM Redundantly Regulate Presynaptic Localization of the Voltage-Gated Calcium Channel in .

机构信息

Laboratory of Neuroscience, Graduate School of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan, and.

Neurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, California 92093.

出版信息

J Neurosci. 2019 Oct 30;39(44):8617-8631. doi: 10.1523/JNEUROSCI.0506-19.2019. Epub 2019 Sep 17.

Abstract

Presynaptic active zones (AZs) contain many molecules essential for neurotransmitter release and are assembled in a highly organized manner. A network of adaptor proteins known as cytomatrix at the AZ (CAZ) is important for shaping the structural characteristics of AZ. Rab3-interacting molecule (RIM)-binding protein (RBP) family are binding partners of the CAZ protein RIM and also bind the voltage-gated calcium channels (VGCCs) in mice and flies. Here, we investigated the physiological roles of RIMB-1, the homolog of RBPs in the nematode RIMB-1 is expressed broadly in neurons and predominantly localized at presynaptic sites. Loss-of-function animals of displayed slight defects in motility and response to pharmacological inhibition of synaptic transmission, suggesting a modest involvement of in synapse function. We analyzed genetic interactions of by testing candidate genes and by an unbiased forward genetic screen for enhancer. Both analyses identified the RIM homolog UNC-10 that acts together with RIMB-1 to regulate presynaptic localization of the P/Q-type VGCC UNC-2/Ca2. We also find that the precise localization of RIMB-1 to presynaptic sites requires presynaptic UNC-2/Ca2. RIMB-1 has multiple FN3 and SH3 domains. Our transgenic rescue analysis with RIMB-1 deletion constructs revealed a functional requirement of a C-terminal SH3 in regulating UNC-2/Ca2 localization. Together, these findings suggest a redundant role of RIMB-1/RBP and UNC-10/RIM to regulate the abundance of UNC-2/Ca2 at the presynaptic AZ in , depending on the bidirectional interplay between CAZ adaptor and channel proteins. Presynaptic active zones (AZs) are highly organized structures for synaptic transmission with characteristic networks of adaptor proteins called cytomatrix at the AZ (CAZ). In this study, we characterized a CAZ protein RIMB-1, named for RIM-binding protein (RBP), in the nematode Through systematic analyses of genetic interactions and an unbiased genetic enhancer screen of , we revealed a redundant role of two CAZ proteins RIMB-1/RBP and UNC-10/RIM in regulating presynaptic localization of UNC-2/Ca2, a voltage-gated calcium channel (VGCC) critical for proper neurotransmitter release. Additionally, the precise localization of RIMB-1/RBP requires presynaptic UNC-2/Ca2. These findings provide new mechanistic insight about how the interplay among multiple CAZ adaptor proteins and VGCC contributes to the organization of presynaptic AZ.

摘要

突触前活性区 (AZ) 包含许多对神经递质释放至关重要的分子,并以高度有序的方式组装。一种称为 AZ 基质 (CAZ) 的衔接蛋白网络对于塑造 AZ 的结构特征很重要。Rab3 相互作用分子 (RIM)-结合蛋白 (RBP) 家族是 CAZ 蛋白 RIM 的结合伴侣,在小鼠和苍蝇中也与电压门控钙通道 (VGCC) 结合。在这里,我们研究了线虫 RIMB-1 的生理作用,RIMB-1 是 RBP 的同源物,在神经元中广泛表达,并主要定位于突触前部位。 显示出运动和对突触传递药理学抑制的反应的轻微缺陷,表明 在突触功能中具有适度的参与。我们通过测试候选基因和进行无偏见的正向遗传筛选来分析 的遗传相互作用。这两种分析都鉴定出 RIM 同源物 UNC-10,它与 RIMB-1 一起调节 P/Q 型 VGCC UNC-2/Ca2 的突触前定位。我们还发现,RIMB-1 精确定位于突触前部位需要突触前 UNC-2/Ca2。RIMB-1 具有多个 FN3 和 SH3 结构域。我们用 RIMB-1 缺失构建体进行的转基因挽救分析表明,C 端 SH3 在调节 UNC-2/Ca2 定位中具有功能要求。总之,这些发现表明,在 中,RIMB-1/RBP 和 UNC-10/RIM 依赖于 CAZ 衔接蛋白和通道蛋白之间的双向相互作用,以冗余的方式调节 UNC-2/Ca2 在突触前 AZ 中的丰度。突触前活性区 (AZ) 是具有特征性衔接蛋白网络的高度有序的突触传递结构,称为 AZ 基质 (CAZ)。在这项研究中,我们在线虫 中描述了一种 CAZ 蛋白 RIMB-1,称为 RIM 结合蛋白 (RBP)。通过对遗传相互作用的系统分析和对 的无偏遗传增强筛选,我们揭示了两个 CAZ 蛋白 RIMB-1/RBP 和 UNC-10/RIM 在调节 UNC-2/Ca2 的突触前定位中的冗余作用,UNC-2/Ca2 是一种对适当神经递质释放至关重要的电压门控钙通道 (VGCC)。此外,RIMB-1/RBP 的精确定位需要突触前 UNC-2/Ca2。这些发现提供了关于多个 CAZ 衔接蛋白和 VGCC 如何相互作用有助于突触前 AZ 组织的新的机制见解。

相似文献

引用本文的文献

10
Presynaptic Cytomatrix Proteins.突触前细胞基质蛋白。
Adv Neurobiol. 2023;33:23-42. doi: 10.1007/978-3-031-34229-5_2.

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验