|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
First published online 1 November 2006
doi: 10.1242/dev.02678
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Research Report |
1 Department of Physiology, Development and Neuroscience, University of
Cambridge, Downing Street, Cambridge CB2 3DY, UK.
2 Division of Engineering and Applied Sciences, Harvard University, Pierce Hall,
29 Oxford Street, Cambridge, MA 02138, USA.
* Author for correspondence (e-mail: rja46{at}cam.ac.uk)
Accepted 4 October 2006
SUMMARY
Mechanisms for shaping and folding sheets of cells during development are poorly understood. An example is the complex reorganisation of the forebrain neural plate during neurulation, which must fold a sheet into a tube while evaginating two eyes from a single contiguous domain within the neural plate. We, for the first time, track these cell rearrangements to show that forebrain morphogenesis differs significantly from prior hypotheses. We postulate a new model for forebrain neurulation and demonstrate how mutations affecting two signalling pathways can generate cyclopic phenotypes by disrupting normal cell movements or introducing new erroneous behaviours.
Key words: Zebrafish, Time-lapse microscopy, Neurulation, Cyclopia, Quantitative analyses
This article has been cited by other articles:
![]() |
P. J. Keller, A. D. Schmidt, J. Wittbrodt, and E. H.K. Stelzer Reconstruction of Zebrafish Early Embryonic Development by Scanned Light Sheet Microscopy Science, November 14, 2008; 322(5904): 1065 - 1069. [Abstract] [Full Text] [PDF] |
||||