Student Author(s)

Sri Devi Narasimhan

UMMS Affiliation

Interdisciplinary Graduate Program, Program in Gene Function and Expression; Program in Molecular Medicine

Date

7-7-2010

Document Type

Article

Medical Subject Headings

Insulin-Like Growth Factor I; Caenorhabditis elegans Proteins; Transcription Factors; Forkhead Transcription Factors; Protein Isoforms; Longevity

Disciplines

Laboratory and Basic Science Research | Life Sciences | Medicine and Health Sciences

Abstract

The insulin/IGF-1 signalling (IIS) pathway has diverse roles from metabolism to longevity. In Caenorhabditis elegans, the single forkhead box O (FOXO) homologue, DAF-16, functions as the major target of the IIS pathway. One of two isoforms, DAF-16a, is known to regulate longevity, stress response and dauer diapause. However, it remains unclear how DAF-16 achieves its specificity in regulating these various biological processes. Here we identify a new isoform, DAF-16d/f, as an important isoform regulating longevity. We show that DAF-16 isoforms functionally cooperate to modulate IIS-mediated processes through differential tissue enrichment, preferential modulation by upstream kinases, and regulating distinct and overlapping target genes. Promoter-swapping experiments show both the promoter and the coding region of DAF-16 are important for its function. Importantly, in mammals, four FOXO genes have overlapping and different functions, and in C. elegans, a single FOXO/DAF-16 uses distinct isoforms to fine-tune the IIS-mediated processes in the context of a whole organism.

Rights and Permissions

Citation: Nature. 2010 Jul 7. [Epub ahead of print]. doi:10.1038/nature09184

Related Resources

Link to article in PubMed