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Letter
Nature 446, 797-800 (12 April 2007) | doi:10.1038/nature05722; Received 31 October 2006; Accepted 26 February 2007; Published online 28 March 2007
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A mirror-symmetric cell division that orchestrates neuroepithelial morphogenesis
Marcel Tawk1, Claudio Araya1, Dave A. Lyons1,4, Alexander M. Reugels2, Gemma C. Girdler1, Philippa R. Bayley1,4, David R. Hyde3, Masazumi Tada1 & Jonathan D. W. Clarke1
- Anatomy and Developmental Biology, UCL, Gower Street, London WC1E 6BT, UK
- Institut für Entwicklungsbiologie, Universität zu Köln, 50923 Köln, Germany
- Department of Biological Sciences and Center for Zebrafish Research, University of Notre Dame, Notre Dame, Indiana 46556, USA
- Present addresses: Department of Developmental Biology, Stanford University School of Medicine, Beckman Center B300, 279 Campus Drive, Stanford, California 94305, USA (D.A.L.); Department of Academic and Student Affairs, Oregon Health and Science University, 3181 SW Sam Jackson Park Road, Portland, Oregon 97239, USA (P.R.B).
Correspondence to: Jonathan D. W. Clarke1 Correspondence and requests for materials should be addressed to J.D.W.C. (Email: jonathan.clarke@ucl.ac.uk).
Abstract
The development of cell polarity is an essential prerequisite for tissue morphogenesis during embryogenesis, particularly in the development of epithelia1, 2. In addition, oriented cell division can have a powerful influence on tissue morphogenesis3. Here we identify a novel mode of polarized cell division that generates pairs of neural progenitors with mirror-symmetric polarity in the developing zebrafish neural tube and has dramatic consequences for the organization of embryonic tissue. We show that during neural rod formation the polarity protein Pard3 is localized to the cleavage furrow of dividing progenitors, and then mirror-symmetrically inherited by the two daughter cells. This allows the daughter cells to integrate into opposite sides of the developing neural tube. Furthermore, these mirror-symmetric divisions have powerful morphogenetic influence: when forced to occur in ectopic locations during neurulation, they orchestrate the development of mirror-image pattern formation and the consequent generation of ectopic neural tubes.
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