Identification of direct DAF-16 targets controlling longevity, metabolism and diapause by chromatin immunoprecipitation
Program in Gene Function and Expression; Program in Molecular Medicine
Alleles; Animals; Caenorhabditis elegans; Caenorhabditis elegans Proteins; Chromatin Immunoprecipitation; Gene Expression Regulation; Genes, Helminth; Longevity; Phenotype; Transcription Factors
Genetics and Genomics
DAF-16, a forkhead transcription factor, is a key regulator of longevity, metabolism and dauer diapause in Caenorhabditis elegans. The precise mechanism by which DAF-16 regulates multiple functions, however, is poorly understood. Here, we used chromatin immunoprecipitation (ChIP) to identify direct targets of DAF-16. We cloned 103 target sequences containing consensus DAF-16 binding sites and selected 33 targets for further analysis. Expression of most of these genes is regulated in a DAF-16-dependent manner, and inactivation of more than half of these genes significantly altered DAF-16-dependent functions, including life span, fat storage and dauer formation. Our results show that the ChIP-based cloning strategy leads to greater enrichment for DAF-16 target genes than previous screening strategies. We also demonstrate that DAF-16 is recruited to multiple promoters to coordinate regulation of its downstream targets. The large number of target genes discovered provides insight into how DAF-16 controls diverse biological functions.
DOI of Published Version
Nat Genet. 2006 Feb;38(2):251-7. Epub 2005 Dec 25. Link to article on publisher's website
Oh SW, Mukhopadhyay A, Dixit BL, Raha T, Green MR, Tissenbaum HA. (2006). Identification of direct DAF-16 targets controlling longevity, metabolism and diapause by chromatin immunoprecipitation. Program in Gene Function and Expression Publications. https://doi.org/10.1038/ng1723. Retrieved from https://escholarship.umassmed.edu/pgfe_pp/148