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Compensatory flux changes within an endocytic trafficking network maintain thermal robustness of Notch signaling.


ABSTRACT: Developmental signaling is remarkably robust to environmental variation, including temperature. For example, in ectothermic animals such as Drosophila, Notch signaling is maintained within functional limits across a wide temperature range. We combine experimental and computational approaches to show that temperature compensation of Notch signaling is achieved by an unexpected variety of endocytic-dependent routes to Notch activation which, when superimposed on ligand-induced activation, act as a robustness module. Thermal compensation arises through an altered balance of fluxes within competing trafficking routes, coupled with temperature-dependent ubiquitination of Notch. This flexible ensemble of trafficking routes supports Notch signaling at low temperature but can be switched to restrain Notch signaling at high temperature and thus compensates for the inherent temperature sensitivity of ligand-induced activation. The outcome is to extend the physiological range over which normal development can occur. Similar mechanisms may provide thermal robustness for other developmental signals.

SUBMITTER: Shimizu H 

PROVIDER: S-EPMC4032575 | biostudies-literature | 2014 May

REPOSITORIES: biostudies-literature

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Compensatory flux changes within an endocytic trafficking network maintain thermal robustness of Notch signaling.

Shimizu Hideyuki H   Woodcock Simon A SA   Wilkin Marian B MB   Trubenová Barbora B   Monk Nicholas A M NA   Baron Martin M  

Cell 20140501 5


Developmental signaling is remarkably robust to environmental variation, including temperature. For example, in ectothermic animals such as Drosophila, Notch signaling is maintained within functional limits across a wide temperature range. We combine experimental and computational approaches to show that temperature compensation of Notch signaling is achieved by an unexpected variety of endocytic-dependent routes to Notch activation which, when superimposed on ligand-induced activation, act as a  ...[more]

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