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在秀丽隐杆线虫的触角轴突导向中,Eph 受体蛋白激酶非依赖性信号传导的机制。

Mechanisms of ephrin receptor protein kinase-independent signaling in amphid axon guidance in Caenorhabditis elegans.

机构信息

Division of Biological Sciences, Section of Cell and Developmental Biology, University of California, San Diego, La Jolla, California 92093.

出版信息

Genetics. 2013 Nov;195(3):899-913. doi: 10.1534/genetics.113.154393. Epub 2013 Aug 26.

Abstract

Eph receptors and their ephrin ligands are key conserved regulators of axon guidance and can function in a variety of signaling modes. Here we analyze the genetic and cellular requirements for Eph signaling in a Caenorhabditis elegans axon guidance choice point, the ventral guidance of axons in the amphid commissure. The C. elegans Eph receptor EFN-1 has both kinase-dependent and kinase-independent roles in amphid ventral guidance. Of the four C. elegans ephrins, we find that only EFN-1 has a major role in amphid axon ventral guidance, and signals in both a receptor kinase-dependent and kinase-independent manner. Analysis of EFN-1 and EFN-1 expression and tissue-specific requirements is consistent with a model in which VAB-1 acts in amphid neurons, interacting with EFN-1 expressed on surrounding cells. Unexpectedly, left-hand neurons are more strongly affected than right-hand neurons by loss of Eph signaling, indicating a previously undetected left-right asymmetry in the requirement for Eph signaling. By screening candidate genes involved in Eph signaling, we find that the Eph kinase-independent pathway involves the ABL-1 nonreceptor tyrosine kinase and possibly the phosphatidylinositol 3-kinase pathway. Overexpression of ABL-1 is sufficient to rescue EFN-1 ventral guidance defects cell autonomously. Our results reveal new aspects of Eph signaling in a single axon guidance decision in vivo.

摘要

Eph 受体及其 Ephrin 配体是轴突导向的关键保守调节因子,可在多种信号模式中发挥作用。在这里,我们分析了 Eph 信号在秀丽隐杆线虫轴突导向选择点(即触角连合中轴突的腹侧导向)中的遗传和细胞需求。秀丽隐杆线虫 Eph 受体 EFN-1 在触角腹侧导向中具有激酶依赖性和非激酶依赖性作用。在四种秀丽隐杆线虫 Ephrin 中,我们发现只有 EFN-1 在触角轴突腹侧导向中起主要作用,并以受体激酶依赖性和非激酶依赖性方式发出信号。对 EFN-1 和 EFN-1 表达的分析以及组织特异性需求的分析与 VAB-1 在触角神经元中起作用的模型一致,与周围细胞表达的 EFN-1 相互作用。出乎意料的是,与 Eph 信号缺失相比,左手神经元比右手神经元受到更大的影响,这表明 Eph 信号的需求存在以前未检测到的左右不对称性。通过筛选涉及 Eph 信号的候选基因,我们发现 Eph 激酶非依赖性途径涉及 ABL-1 非受体酪氨酸激酶,并且可能涉及磷脂酰肌醇 3-激酶途径。ABL-1 的过表达足以自主挽救 EFN-1 腹侧导向缺陷。我们的结果揭示了 Eph 信号在体内单个轴突导向决策中的新方面。

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