Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA, United States.
Curr Top Dev Biol. 2018;127:1-21. doi: 10.1016/bs.ctdb.2017.11.007. Epub 2018 Feb 2.
In Caenorhabditis elegans, there is a single FOXO transcription factor homolog, encoded by the gene, daf-16. As a central regulator for multiple signaling pathways, DAF-16 integrates these signals which results in modulation of several biological processes including longevity, development, fat storage, stress resistance, innate immunity, and reproduction. Using C. elegans allows for studies of FOXO in the context of the whole animal. Therefore, manipulating levels or the activity of daf-16 results in phenotypic changes. Genetic and molecular analysis revealed that similar to other systems, DAF-16 is the downstream target of the conserved insulin/IGF-1 signaling (IIS) pathway; a PI 3-kinase/AKT signaling cascade that ultimately controls the regulation of DAF-16 nuclear localization. In this chapter, I will focus on understanding how a single gene daf-16 can incorporate signals from multiple upstream pathways and in turn modulate different phenotypes as well as the study of FOXO in the context of a whole organism.
在秀丽隐杆线虫中,存在一个单一的 FOXO 转录因子同源物,由基因 daf-16 编码。作为多种信号通路的中央调节剂,DAF-16 整合这些信号,从而调节包括寿命、发育、脂肪储存、应激抗性、先天免疫和生殖在内的多种生物学过程。使用秀丽隐杆线虫可以在整个动物体内研究 FOXO。因此,操纵 daf-16 的水平或活性会导致表型变化。遗传和分子分析表明,与其他系统相似,DAF-16 是保守的胰岛素/IGF-1 信号(IIS)途径的下游靶标;一种 PI 3-激酶/AKT 信号级联,最终控制 DAF-16 核定位的调节。在本章中,我将重点研究单个基因 daf-16 如何整合来自多个上游途径的信号,以及如何反过来调节不同的表型,以及在整个生物体中研究 FOXO。