spacer gif spacer gif spacer gif spacer gif ARCHIVE ANNOUNCEMENT! spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Saude, L.
Right arrow Articles by Stemple, D. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Saude, L.
Right arrow Articles by Stemple, D. L.

Development, Vol 127, Issue 16 3407-3417, Copyright © 2000 by Company of Biologists


JOURNAL ARTICLES

Axis-inducing activities and cell fates of the zebrafish organizer

L Saude, K Woolley, P Martin, W Driever and DL Stemple
Division of Developmental Biology, National Institute for Medical Research, Mill Hill, London NW7 1AA, UK.

We have investigated axis-inducing activities and cellular fates of the zebrafish organizer using a new method of transplantation that allows the transfer of both deep and superficial organizer tissues. Previous studies have demonstrated that the zebrafish embryonic shield possesses classically defined dorsal organizer activity. When we remove the morphologically defined embryonic shield, embryos recover and are completely normal by 24 hours post-fertilization. We find that removal of the morphological shield does not remove all goosecoid- and floating head-expressing cells, suggesting that the morphological shield does not comprise the entire organizer region. Complete removal of the embryonic shield and adjacent marginal tissue, however, leads to a loss of both prechordal plate and notochord. In addition, these embryos are cyclopean, show a significant loss of floor plate and primary motorneurons and display disrupted somite patterning. Motivated by apparent discrepancies in the literature we sought to test the axis-inducing activity of the embryonic shield. A previous study suggested that the shield is capable of only partial axis induction, specifically being unable to induce the most anterior neural tissues. Contrary to this study, we find shields can induce complete secondary axes when transplanted into host ventral germ-ring. In induced secondary axes donor tissue contributes to notochord, prechordal plate and floor plate. When explanted shields are divided into deep and superficial fragments and separately transplanted we find that deep tissue is able to induce the formation of ectopic axes with heads but lacking posterior tissues. We conclude that the deep tissue included in our transplants is important for proper head formation.


This article has been cited by other articles:


Home page
DevelopmentHome page
C. Chang and R. M. Harland
Neural induction requires continued suppression of both Smad1 and Smad2 signals during gastrulation
Development, November 1, 2007; 134(21): 3861 - 3872.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
G. Reim and M. Brand
Maternal control of vertebrate dorsoventral axis formation and epiboly by the POU domain protein Spg/Pou2/Oct4
Development, July 15, 2006; 133(14): 2757 - 2770.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
C. E. Burns, D. Traver, E. Mayhall, J. L. Shepard, and L. I. Zon
Hematopoietic stem cell fate is established by the Notch-Runx pathway
Genes & Dev., October 1, 2005; 19(19): 2331 - 2342.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
D. L. Stemple
Structure and function of the notochord: an essential organ for chordate development
Development, June 1, 2005; 132(11): 2503 - 2512.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
M. Rhinn, K. Lun, M. Luz, M. Werner, and M. Brand
Positioning of the midbrain-hindbrain boundary organizer through global posteriorization of the neuroectoderm mediated by Wnt8 signaling
Development, March 15, 2005; 132(6): 1261 - 1272.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
J. S. Zoltewicz, N. J. Stewart, R. Leung, and A. S. Peterson
Atrophin 2 recruits histone deacetylase and is required for the function of multiple signaling centers during mouse embryogenesis
Development, January 1, 2004; 131(1): 3 - 14.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
M. J. Parsons, S. M. Pollard, L. Saude, B. Feldman, P. Coutinho, E. M. A. Hirst, and D. L. Stemple
Zebrafish mutants identify an essential role for laminins in notochord formation
Development, January 7, 2002; 129(13): 3137 - 3146.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
C. E. Erter, T. P. Wilm, N. Basler, C. V. E. Wright, and L. Solnica-Krezel
Wnt8 is required in lateral mesendodermal precursors for neural posteriorization in vivo
Development, September 15, 2001; 128(18): 3571 - 3583.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
C.-P. Heisenberg, C. Houart, M. Take-uchi, G.-J. Rauch, N. Young, P. Coutinho, I. Masai, L. Caneparo, M. L. Concha, R. Geisler, et al.
A mutation in the Gsk3-binding domain of zebrafish Masterblind/Axin1 leads to a fate transformation of telencephalon and eyes to diencephalon
Genes & Dev., June 1, 2001; 15(11): 1427 - 1434.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 2000