Worming pathways to and from DAF-16/FOXO

Mukhopadhyay, Arnab ; Oh, Seung Wook ; Tissenbaum, Heidi A. (2006) Worming pathways to and from DAF-16/FOXO Experimental Gerontology, 41 (10). pp. 928-934. ISSN 0531-5565

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Official URL: http://doi.org/10.1016/j.exger.2006.05.020

Related URL: http://dx.doi.org/10.1016/j.exger.2006.05.020

Abstract

In Caenorhabditis elegans, the insulin/IGF-1 signaling pathway controls many biological processes such as life span, fat storage, dauer diapause, reproduction and stress response Barbieri et al., 2003. This pathway is comprised of many genes including the insulin/IGF-1 receptor (DAF-2) that signals through a conserved PI 3-kinase/AKT pathway and ultimately down-regulates DAF-16, a forkhead transcription factor (FOXO). DAF-16 also receives input from several other pathways that regulate life span such as the germline and the JNK pathway [Hsin, H., Kenyon, C., 1999. Signals from the reproductive system regulate the lifespan of C. elegans. Nature 399, 362–366; Oh, S.W., Mukhopadhyay, A., Svrzikapa, N., Jiang, F., Davis, R.J., Tissenbaum, H.A., 2005. JNK regulates lifespan in Caenorhabditis elegans by modulating nuclear translocation of forkhead transcription factor/DAF-16. Proc. Natl. Acad. Sci. USA 102, 4494–4499]. Therefore, DAF-16 integrates signals from multiple pathways and regulates its downstream target genes to control diverse processes. Here, we discuss the signals to and from DAF-16, with a focus on life span regulation.

Item Type:Article
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