The C. elegans adult neuronal IIS/FOXO transcriptome reveals adult phenotype regulators.

TitleThe C. elegans adult neuronal IIS/FOXO transcriptome reveals adult phenotype regulators.
Publication TypeJournal Article
Year of Publication2016
AuthorsKaletsky, R, Lakhina, V, Arey, R, Williams, A, Landis, J, Ashraf, J, Murphy, CT
JournalNature
Volume529
Issue7584
Pagination92-6
Date Published2016 Jan 7
ISSN1476-4687
KeywordsAging, Animals, Axons, Caenorhabditis elegans, Caenorhabditis elegans Proteins, Cell Separation, Forkhead Transcription Factors, Insulin, Longevity, Mechanotransduction, Cellular, Memory, Mutation, Neurons, Phenotype, Regeneration, Signal Transduction, Somatomedins, Transcriptome
Abstract

<p>Insulin/insulin-like growth factor signalling (IIS) is a critical regulator of an organism's most important biological decisions from growth, development, and metabolism to reproduction and longevity. It primarily does so through the activity of the DAF-16 transcription factor (forkhead box O (FOXO) homologue), whose global targets were identified in Caenorhabditis elegans using whole-worm transcriptional analyses more than a decade ago. IIS and FOXO also regulate important neuronal and adult behavioural phenotypes, such as the maintenance of memory and axon regeneration with age, in both mammals and C. elegans, but the neuron-specific IIS/FOXO targets that regulate these functions are still unknown. By isolating adult C. elegans neurons for transcriptional profiling, we identified both the wild-type and IIS/FOXO mutant adult neuronal transcriptomes for the first time. IIS/FOXO neuron-specific targets are distinct from canonical IIS/FOXO-regulated longevity and metabolism targets, and are required for extended memory in IIS daf-2 mutants. The activity of the forkhead transcription factor FKH-9 in neurons is required for the ability of daf-2 mutants to regenerate axons with age, and its activity in non-neuronal tissues is required for the long lifespan of daf-2 mutants. Together, neuron-specific and canonical IIS/FOXO-regulated targets enable the coordinated extension of neuronal activities, metabolism, and longevity under low-insulin signalling conditions.</p>

DOI10.1038/nature16483
Alternate JournalNature
PubMed ID26675724
PubMed Central IDPMC4708089
Grant ListDP1 GM119167 / GM / NIGMS NIH HHS / United States
R01 AG034446 / AG / NIA NIH HHS / United States
T32 HG003284 / HG / NHGRI NIH HHS / United States