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Nature 449, 183-188 (13 September 2007) | doi:10.1038/nature06100; Received 5 February 2007; Accepted 18 July 2007; Published online 29 August 2007

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MicroRNA control of Nodal signalling

Graziano Martello1, Luca Zacchigna1, Masafumi Inui1, Marco Montagner1, Maddalena Adorno1, Anant Mamidi1, Leonardo Morsut1, Sandra Soligo1, Uyen Tran2, Sirio Dupont1, Michelangelo Cordenonsi1, Oliver Wessely2 & Stefano Piccolo1

  1. Department of Histology, Microbiology and Medical Biotechnologies, Section of Histology and Embryology, University of Padua, viale Colombo 3, 35126 Padua, Italy
  2. Departments of Cell Biology & Anatomy and Genetics, LSU Health Sciences Center, 1901 Perdido Street, New Orleans, Louisiana 70112, USA

Correspondence to: Stefano Piccolo1 Correspondence and requests for materials should be addressed to S.P. (Email: piccolo@bio.unipd.it).

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MicroRNAs are crucial modulators of gene expression, yet their involvement as effectors of growth factor signalling is largely unknown. Ligands of the transforming growth factor-beta superfamily are essential for development and adult tissue homeostasis. In early Xenopus embryos, signalling by the transforming growth factor-beta ligand Nodal is crucial for the dorsal induction of the Spemann's organizer. Here we report that Xenopus laevis microRNAs miR-15 and miR-16 restrict the size of the organizer by targeting the Nodal type II receptor Acvr2a. Endogenous miR-15 and miR-16 are ventrally enriched as they are negatively regulated by the dorsal Wnt/beta-catenin pathway. These findings exemplify the relevance of microRNAs as regulators of early embryonic patterning acting at the crossroads of fundamental signalling cascades.

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