Division of Biological Sciences, Section of Cell and Developmental Biology, University of California, San Diego, La Jolla, California 92093.
Genetics. 2013 Nov;195(3):899-913. doi: 10.1534/genetics.113.154393. Epub 2013 Aug 26.
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.
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。