Pervasive Positive and Negative Feedback Regulation of Insulin-Like Signaling inCaenorhabditis elegans
Author(s) -
Rebecca E. W. Kaplan,
Colin S. Maxwell,
Nicole Kurhanewicz Codd,
L. Ryan Baugh
Publication year - 2018
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1534/genetics.118.301702
Subject(s) - biology , caenorhabditis elegans , insulin receptor , signal transduction , transcription factor , microbiology and biotechnology , insulin , nutrient sensing , glucose homeostasis , genetics , gene , insulin resistance , endocrinology
The Caenorhabditis elegans genome encodes 40 insulin-like peptides, but the dynamics of insulin signaling both during development and in response to nutrient availability is not well understood. Kaplan and Maxwell et al. report that transcription of.... The Caenorhabditis elegans insulin-like signaling network supports homeostasis and developmental plasticity. The genome encodes 40 insulin-like peptides and one known receptor. Feedback regulation has been reported, but the extent of feedback and its effect on signaling dynamics in response to changes in nutrient availability has not been determined. We measured messenger RNA expression for each insulin-like peptide, the receptor daf-2, components of the PI3K pathway, and its transcriptional effectors daf-16/FoxO and skn-1/Nrf at high temporal resolution during transition from a starved, quiescent state to a fed, growing state in wild type and mutants affecting daf-2/InsR and daf-16/FoxO. We also analyzed the effect of temperature on insulin-like gene expression. We found that most PI3K pathway components and insulin-like peptides are affected by signaling activity, revealing pervasive positive and negative feedback regulation at intra- and intercellular levels. Reporter gene analysis demonstrated that the daf-2/InsR agonist daf-28 positively regulates its own transcription and that the putative agonist ins-6 cross-regulates DAF-28 protein expression through feedback. Our results show that positive and negative feedback regulation of insulin-like signaling is widespread, giving rise to an organismal FoxO-to-FoxO signaling network that supports homeostasis during fluctuations in nutrient availability.
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