The Ral small GTPase in C. elegans development

线虫发育中的 Ral 小 GTP 酶

• 批准号: 8788470
• 负责人: David Reiner
• 金额: $ 9.07万
• 依托单位: TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-04-01 至 2015-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8788470
• 关键词: Ral; small; GTPase; C.; elegans

DESCRIPTION (provided by applicant: Ras is the most frequently mutated oncogene in human cancers and the Raf-MEK-ERK protein kinase cascade is the best characterized downstream effector function of Ras. However, it is now clear that Ras function cannot be ascribed simply to one effector pathway, and that Ras utilizes a spectrum of functionally diverse effectors, with at least five implicated in oncogenesis. What remains unclear is how effector utilization is regulated. Recent studies have implicated a critical role for guanine nucleotide exchange factors for the Ral small GTPases (RalGEFs) as effectors of Ras in cancer. Yet we know little about the interplay between RalGEF-Ral and other effector pathways, and we know even less about the normal functions of RalGEF-Ral activity during development. Genetic analyses of the Ras homolog in C. elegans, LET-60, have elucidated the role of the Raf-MEK-ERK cascade in development and provided critical clues for understanding mechanisms of Ras signaling in mammalian cells. Since essentially all known components of RalGEF-Ral signaling are conserved in C. elegans, this prompted our interest in elucidating a role for the evolutionarily conserved C. elegans RGL-1 (RalGEF) and RAL-1 (Ral) in LET-60-regulated development. Our preliminary results indicate that, unexpectedly, RGL-1-RAL-1 signaling antagonized rather than cooperated with the Raf-MEK-ERK signal in inducing 10 cell fate in the vulva, and does so in parallel or downstream to the ERK substrate, the LIN- 31/HNF transcription factor. Additionally, our results suggest that RAL-1 is expressed only in 20 cells neighboring 10 vulval cells, suggesting that LET-60/Ras switches from the use of one effector (LIN-45/Raf) in 10 cells to another (RGL-1/RalGEF) in 20 cells, and that RAL-1 controls the balance of Ras-dependent cell fates. These observations provide the rationale for our analysis of the role of RGL-1-RAL-1 signaling in cell fate induction, a model for RalGEF-Ral oncogenic functions, and to our knowledge the first developmental model to study the potentially critical regulatory mechanism of differential effector usage by Ras. We propose studies that will apply a multi-faceted approach that utilizes genetic, biochemical and cell biological methods to elucidate the mechanisms and roles by which LET-60 dynamically regulates these two distinct effector- signaling networks. We propose aims to (1) determine the signaling properties of the RGL-1-RAL-1 module relative to the Ras-Raf-MEK-ERK pathway, (2) determine the developmental mechanisms by which RGL-1- RAL-1 controls equivalence group fate decisions, and (3) determine the genetic and molecular mechanism of RGL-1-RAL-1 function in 20 cells. Our studies will address outstanding questions of developmental patterning in response to a morphogen gradient, balance between Ras and Notch signaling, and differential use of effectors in development and cancer, all of which lie at a critical intersection between developmental biology and cancer.

描述（由申请人提供：Ras是人类癌症中最常突变的癌基因，Raf-MEK-ERK蛋白激酶级联是Ras的最佳表征的下游效应子功能。然而，现在很清楚，Ras功能不能简单地归因于一个效应子途径，Ras利用一系列功能多样的效应子，其中至少有五个与肿瘤发生有关。目前尚不清楚的是效应子的利用是如何调节的。最近的研究表明，鸟嘌呤核苷酸交换因子作为Ras在癌症中的效应物，对Ral小GTP酶（RalGEF）起着关键作用。然而，我们对RalGEF-Ral和其他效应通路之间的相互作用知之甚少，我们对发育过程中RalGEF-Ral活性的正常功能了解更少。对C. elegans，LET-60，阐明了Raf-MEK-ERK级联在发育中的作用，并为理解哺乳动物细胞中Ras信号传导机制提供了重要线索。由于RalGEF-Ral信号传导的基本上所有已知组分在C. elegans，这促使我们有兴趣阐明进化上保守的C。elegans RGL-1（RalGEF）和RAL-1（Ral）在LET-60调节的发育中的作用。我们的初步结果表明，出乎意料的是，RGL-1-RAL-1信号传导拮抗而不是与Raf-MEK-ERK信号在外阴中诱导10细胞命运，并且与ERK底物LIN- 31/HNF转录因子平行或下游地这样做。此外，我们的研究结果表明，RAL-1只在20个细胞中表达相邻的10个外阴细胞，这表明，LET-60/Ras开关从使用一个效应器（LIN-45/Raf）在10个细胞到另一个（RGL-1/RalGEF）在20个细胞，和RAL-1控制的Ras依赖性细胞命运的平衡。这些观察结果为我们分析RGL-1-RAL-1信号传导在细胞命运诱导中的作用提供了理论基础，这是RalGEF-Ral致癌功能的模型，据我们所知，这是研究Ras对差异效应子使用的潜在关键调节机制的第一个发育模型。我们提出的研究将应用多方面的方法，利用遗传，生物化学和细胞生物学方法来阐明LET-60动态调节这两个不同的效应器信号网络的机制和作用。我们提出的目的是（1）确定RGL-1-RAL-1模块相对于Ras-Raf-MEK-ERK通路的信号传导特性，（2）确定RGL-1- RAL-1控制等效组命运决定的发育机制，以及（3）确定20个细胞中RGL-1-RAL-1功能的遗传和分子机制。我们的研究将解决发育模式的突出问题，以响应形态梯度，Ras和Notch信号之间的平衡，以及在发育和癌症中效应子的差异化使用，所有这些都位于发育生物学和癌症之间的关键交叉点。