Author
Listed:
- Julien Prudent
(Université de Lyon, Centre de recherche en cancérologie de Lyon, U1052 INSERM, UMS 3453 CNRS, Université Lyon I, Centre Léon Bérard, 28 rue Laennec)
- Nikolay Popgeorgiev
(Université de Lyon, Centre de recherche en cancérologie de Lyon, U1052 INSERM, UMS 3453 CNRS, Université Lyon I, Centre Léon Bérard, 28 rue Laennec)
- Benjamin Bonneau
(Université de Lyon, Centre de recherche en cancérologie de Lyon, U1052 INSERM, UMS 3453 CNRS, Université Lyon I, Centre Léon Bérard, 28 rue Laennec)
- Julien Thibaut
(Université de Lyon, Centre de recherche en cancérologie de Lyon, U1052 INSERM, UMS 3453 CNRS, Université Lyon I, Centre Léon Bérard, 28 rue Laennec)
- Rudy Gadet
(Université de Lyon, Centre de recherche en cancérologie de Lyon, U1052 INSERM, UMS 3453 CNRS, Université Lyon I, Centre Léon Bérard, 28 rue Laennec)
- Jonathan Lopez
(Université de Lyon, Centre de recherche en cancérologie de Lyon, U1052 INSERM, UMS 3453 CNRS, Université Lyon I, Centre Léon Bérard, 28 rue Laennec
Hospices Civils de Lyon, Fédération de Biochimie Nord, Hôpital de la Croix-Rousse, 103 Grande rue de la Croix-Rousse)
- Philippe Gonzalo
(Université de Lyon, Centre de recherche en cancérologie de Lyon, U1052 INSERM, UMS 3453 CNRS, Université Lyon I, Centre Léon Bérard, 28 rue Laennec
Hospices Civils de Lyon, Fédération de Biochimie Nord, Hôpital de la Croix-Rousse, 103 Grande rue de la Croix-Rousse)
- Ruth Rimokh
(Université de Lyon, Centre de recherche en cancérologie de Lyon, U1052 INSERM, UMS 3453 CNRS, Université Lyon I, Centre Léon Bérard, 28 rue Laennec)
- Stephen Manon
(Université de Bordeaux, Institut de génétique et biochimie cellulaires, UMR 5095 CNRS, 1 rue Camille Saint-Saëns)
- Corinne Houart
(MRC Centre for Developmental Neurobiology, King’s college, University of London, NHH, Guy’s Campus)
- Philippe Herbomel
(CNRS-URA 2578, Institut Pasteur, 25 rue du Dr Roux)
- Abdel Aouacheria
(Laboratoire de Biologie Moléculaire de la Cellule, Ecole Normale Supérieure de Lyon, UMR 5239 CNRS–UCBL–ENS Lyon, Université de Lyon, SFR BioSciences Gerland, Lyon Sud (UMS3444/US8), 46 Allée d’Italie)
- Germain Gillet
(Université de Lyon, Centre de recherche en cancérologie de Lyon, U1052 INSERM, UMS 3453 CNRS, Université Lyon I, Centre Léon Bérard, 28 rue Laennec)
Abstract
Bcl-2 proteins are acknowledged as key regulators of programmed cell death. However, increasing data suggest additional roles, including regulation of the cell cycle, metabolism and cytoskeletal dynamics. Here we report the discovery and characterization of a new Bcl-2-related multidomain apoptosis accelerator, Bcl-wav, found in fish and frogs. Genetic and molecular studies in zebrafish indicate that Bcl-wav and the recently identified mitochondrial calcium uniporter (MCU) contribute to the formation of the notochord axis by controlling blastomere convergence and extension movements during gastrulation. Furthermore, we found that Bcl-wav controls intracellular Ca2+ trafficking by acting on the mitochondrial voltage-dependent anion channel, and possibly on MCU, with direct consequences on actin microfilament dynamics and blastomere migration guidance. Thus, from an evolutionary point of view, the original function of Bcl-2 proteins might have been to contribute in controlling the global positioning system of blastomeres during gastrulation, a critical step in metazoan development.
Suggested Citation
Julien Prudent & Nikolay Popgeorgiev & Benjamin Bonneau & Julien Thibaut & Rudy Gadet & Jonathan Lopez & Philippe Gonzalo & Ruth Rimokh & Stephen Manon & Corinne Houart & Philippe Herbomel & Abdel Aou, 2013.
"Bcl-wav and the mitochondrial calcium uniporter drive gastrula morphogenesis in zebrafish,"
Nature Communications, Nature, vol. 4(1), pages 1-15, December.
Handle:
RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms3330
DOI: 10.1038/ncomms3330
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