Sundaram M, Han M
Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder 80309-347, USA.
Bioessays. 1996 Jun;18(6):473-80. doi: 10.1002/bies.950180609.
Vulval development in the Caenorhabditis elegans hermaphrodite represents a simple, genetically tractable system for studying how cell signaling events control cell fate decisions. Current models suggest that proper specification of vulval cell fates relies on the integration of multiple signaling systems, including one that involves a receptor tyrosine kinase (RTK)-->Ras-->mitogen activated protein kinase (MAPK) cascade and one that involves a LIN-12/Notch family receptor. In this review, we first discuss how genetic strategies are being used to identify and analyze components that control vulval cell fate decisions. We then describe the different signaling systems that have been elucidated and how they relate to one another. Finally, we highlight several recently characterized genes that encode positive regulators, negative regulators or potential targets of the RTK-->Ras-->MAPK cascade involved in vulval induction.
秀丽隐杆线虫雌雄同体的外阴发育代表了一个简单的、具有遗传易处理性的系统,用于研究细胞信号事件如何控制细胞命运决定。目前的模型表明,外阴细胞命运的正确指定依赖于多种信号系统的整合,其中一个涉及受体酪氨酸激酶(RTK)→Ras→丝裂原活化蛋白激酶(MAPK)级联反应,另一个涉及LIN-12/Notch家族受体。在这篇综述中,我们首先讨论如何利用遗传策略来识别和分析控制外阴细胞命运决定的成分。然后,我们描述已阐明的不同信号系统以及它们之间的相互关系。最后,我们重点介绍了几个最近鉴定的基因,这些基因编码参与外阴诱导的RTK→Ras→MAPK级联反应的正调控因子、负调控因子或潜在靶点。