Abelson蛋白c端结构域的第1 / 4调控WAVE调控复合体和轴突引导中的Enabled。

IF 4 3区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Han Sian Joshua Cheong, Mark Nona, Samantha Barbara Guerra, Mark Francis VanBerkum
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引用次数: 8

摘要

背景:Abelson酪氨酸激酶(Abl)在连接引导受体与肌动蛋白动力学的轴突引导中起关键作用。果蝇Abl的长c端结构域(CTD)对这一作用很重要,以前的工作确定了CTD的“第一季度”(1Q)是必不可少的。在这里,我们将1Q结合伙伴的物理相互作用与Abl在轴突引导中的功能联系起来。方法:采用GST下拉法和质谱法鉴定1Q蛋白结合伙伴,并在胚胎神经索和运动神经元中采用轴突引导法进行验证。利用一系列Abl转基因与突变或过表达的下拉蛋白基因及其在肌动蛋白动力学中的伙伴基因结合,从遗传学角度评估了1Q的作用。这组Abl转基因有以下区域被删除:所有的1Q, 1Q的每一半('eighths', 1E和2E)或2E中的PxxP基序,它可能结合SH3结构域。结果:GST pulldown发现Hem和Sra-1是1Q的结合伙伴,我们的遗传分析表明这两种蛋白在轴突引导中与Abl一起起作用,Sra-1可能与1Q相互作用。由于Hem和Sra-1是肌动蛋白聚合WAVE调节复合体(WRC)的一部分,我们将分析扩展到Abi和Trio,它们与Abl和WRC成员相互作用。总的来说,1Q区域(尤其是2E和它的PxxP基序)对于Abl在轴突引导中与WRC一起工作的能力很重要。这些区域对于Abl在激活肌动蛋白调节因子时的功能也很重要。相比之下,1E对位于中线的WRC的Abl功能有贡献,但对Enabled的贡献较小。结论:1Q区域,特别是带有PxxP基序的2E区域,将Abl与WRC、其调控因子Trio和Abi以及肌动蛋白调控因子Ena连接起来。去除1E具有特定的影响,这表明它可能有助于调节Abl与WRC或Ena的相互作用。因此,Abl的1Q区域在轴突引导过程中调节肌动蛋白动力学中起关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The first quarter of the C-terminal domain of Abelson regulates the WAVE regulatory complex and Enabled in axon guidance.

The first quarter of the C-terminal domain of Abelson regulates the WAVE regulatory complex and Enabled in axon guidance.

The first quarter of the C-terminal domain of Abelson regulates the WAVE regulatory complex and Enabled in axon guidance.

The first quarter of the C-terminal domain of Abelson regulates the WAVE regulatory complex and Enabled in axon guidance.

Background: Abelson tyrosine kinase (Abl) plays a key role in axon guidance in linking guidance receptors to actin dynamics. The long C-terminal domain (CTD) of Drosophila Abl is important for this role, and previous work identified the 'first quarter' (1Q) of the CTD as essential. Here, we link the physical interactions of 1Q binding partners to Abl's function in axon guidance.

Methods: Protein binding partners of 1Q were identified by GST pulldown and mass spectrometry, and validated using axon guidance assays in the embryonic nerve cord and motoneurons. The role of 1Q was assessed genetically, utilizing a battery of Abl transgenes in combination with mutation or overexpression of the genes of pulled down proteins, and their partners in actin dynamics. The set of Abl transgenes had the following regions deleted: all of 1Q, each half of 1Q ('eighths', 1E and 2E) or a PxxP motif in 2E, which may bind SH3 domains.

Results: GST pulldown identified Hem and Sra-1 as binding partners of 1Q, and our genetic analyses show that both proteins function with Abl in axon guidance, with Sra-1 likely interacting with 1Q. As Hem and Sra-1 are part of the actin-polymerizing WAVE regulatory complex (WRC), we extended our analyses to Abi and Trio, which interact with Abl and WRC members. Overall, the 1Q region (and especially 2E and its PxxP motif) are important for Abl's ability to work with WRC in axon guidance. These areas are also important for Abl's ability to function with the actin regulator Enabled. In comparison, 1E contributes to Abl function with the WRC at the midline, but less so with Enabled.

Conclusions: The 1Q region, and especially the 2E region with its PxxP motif, links Abl with the WRC, its regulators Trio and Abi, and the actin regulator Ena. Removing 1E has specific effects suggesting it may help modulate Abl's interaction with the WRC or Ena. Thus, the 1Q region of Abl plays a key role in regulating actin dynamics during axon guidance.

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来源期刊
Neural Development
Neural Development 生物-发育生物学
CiteScore
6.60
自引率
0.00%
发文量
11
审稿时长
>12 weeks
期刊介绍: Neural Development is a peer-reviewed open access, online journal, which features studies that use molecular, cellular, physiological or behavioral methods to provide novel insights into the mechanisms that underlie the formation of the nervous system. Neural Development aims to discover how the nervous system arises and acquires the abilities to sense the world and control adaptive motor output. The field includes analysis of how progenitor cells form a nervous system during embryogenesis, and how the initially formed neural circuits are shaped by experience during early postnatal life. Some studies use well-established, genetically accessible model systems, but valuable insights are also obtained from less traditional models that provide behavioral or evolutionary insights.
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