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All animals coordinate growth and maturation to reach theirfinal size and shape. In insects, insulin family molecules controlgrowth and metabolism, whereas pulses of the steroid 20-hydroxyecdysone(20E) initiate major developmental transitions. We show that20E signaling also negatively controls animal growth rates byimpeding general insulin signaling involving localization ofthe transcription factor dFOXO and transcription of the translationinhibitor 4E-BP. We also demonstrate that the larval fat body,equivalent to the vertebrate liver, is a key relay element forecdysone-dependent growth inhibition. Hence, ecdysone counteractsthe growth-promoting action of insulins, thus forming a humoralregulatory loop that determines organismal size.
1 CNRS/University of NiceSophia Antipolis, UMR6543, Parc Valrose, 06108 Nice Cedex 2, France. 2 CNRS FRE2852, Université P. et M. Curie, 7 quai St. Bernard, 75252 Paris, France. 3 Institut Pasteur, 25-28 rue du Docteur Roux, 75724 Paris, France.
* These authors contributed equally to this work.
Present address: Cancer Research UK, London Institute, 44 Lincoln'sInn Fields, London WC2A 3PX, UK.
To whom correspondence should be addressed. E-mail: leopold{at}unice.fr
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