spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

First published online December 1, 2003
doi: 10.1242/10.1242/dev.00899


Development 130, 6611-6623 (2003)
Published by The Company of Biologists 2003


This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
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 Related articles in Development
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 Jászai, J.
Right arrow Articles by Brand, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Jászai, J.
Right arrow Articles by Brand, M.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Isthmus-to-midbrain transformation in the absence of midbrain-hindbrain organizer activity

József Jászai1,2, Frank Reifers1,2, Alexander Picker1,2, Tobias Langenberg1,2 and Michael Brand1,2,*

1 Max Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstraße 108, 01307 Dresden, Germany
2 Department of Genetics, University of Technology, Dresden, Germany

* Author for correspondence (e-mail: brand{at}mpi-cbg.de)

Accepted 18 September 2003

In zebrafish acerebellar (ace) embryos, because of a point mutation in fgf8, the isthmic constriction containing the midbrain-hindbrain boundary (MHB) organizer fails to form. The mutants lack cerebellar development by morphological criteria, and they appear to have an enlarged tectum, showing no obvious reduction in the tissue mass at the dorsal mesencephalic/metencephalic alar plate. To reveal the molecular identity of the tissues located at equivalent rostrocaudal positions along the neuraxis as the isthmic and cerebellar primordia in wild-types, we undertook a detailed analysis of ace embryos. In ace mutants, the appearance of forebrain and midbrain specific marker genes (otx2, dmbx1, wnt4) in the caudal tectal enlargement reveals a marked rostralized gene expression profile during early somitogenesis, followed by the lack of early and late cerebellar-specific gene expression (zath1/atoh1, gap43, tag1/cntn2, neurod, zebrin II). The Locus coeruleus (LC) derived from rostral rhombomere 1 is also absent in the mutants. A new interface between otx2 and epha4a suggests that the rostralization stops at the caudal part of rhombomere 1. The mesencephalic basal plate is also affected in the mutant embryos, as indicated by the caudal expansion of the diencephalic expression domains of epha4a, zash1b/ashb, gap43 and tag1/cntn2, and by the dramatic reduction of twhh expression. No marked differences are seen in cell proliferation and apoptotic patterns around the time the rostralization of gene expression becomes evident in the mutants. Therefore, locally distinct cell proliferation and cell death is unlikely to be the cause of the fate alteration of the isthmic and cerebellar primordia in the mutants. Dil cell-lineage labeling of isthmic primordial cells reveals that cells, at the location equivalent of the wild-type MHB, give rise to caudal tectum in ace embryos. This suggests that a caudalto-rostral transformation leads to the tectal expansion in the mutants. Fgf8-coated beads are able to rescue morphological MHB formation, and elicit the normal molecular identity of the isthmic and cerebellar primordium in ace embryos. Taken together, our analysis reveals that cells of the isthmic and cerebellar primordia acquire a more rostral, tectal identity in the absence of the functional MHB organizer signal Fgf8.

Key words: ace, acerebellar, Fgf8, Midbrain, Hindbrain, Cerebellum, isthmus rhombencephali, MHB, Rhombomere 1, Rostralization, Transformation, Patterning, Lineage analysis, Bead implantation, Plasticity, Modularity, Zebrafish, D. rerio


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?

Related articles in Development:

A change of mind

Development 2003 130: 2605. [Full Text]  



This article has been cited by other articles:


Home page
DevelopmentHome page
T. Sato and A. L. Joyner
The duration of Fgf8 isthmic organizer expression is key to patterning different tectal-isthmo-cerebellum structures
Development, November 1, 2009; 136(21): 3617 - 3626.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
K. S. Imai, A. Stolfi, M. Levine, and Y. Satou
Gene regulatory networks underlying the compartmentalization of the Ciona central nervous system
Development, January 15, 2009; 136(2): 285 - 293.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
J. Saarimaki-Vire, P. Peltopuro, L. Lahti, T. Naserke, A. A. Blak, D. M. Vogt Weisenhorn, K. Yu, D. M. Ornitz, W. Wurst, and J. Partanen
Fibroblast Growth Factor Receptors Cooperate to Regulate Neural Progenitor Properties in the Developing Midbrain and Hindbrain
J. Neurosci., August 8, 2007; 27(32): 8581 - 8592.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
I. Foucher, M. Mione, A. Simeone, D. Acampora, L. Bally-Cuif, and C. Houart
Differentiation of cerebellar cell identities in absence of Fgf signalling in zebrafish Otx morphants
Development, May 15, 2006; 133(10): 1891 - 1900.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
E. E. Storm, S. Garel, U. Borello, J. M. Hebert, S. Martinez, S. K. McConnell, G. R. Martin, and J. L. R. Rubenstein
Dose-dependent functions of Fgf8 in regulating telencephalic patterning centers
Development, May 1, 2006; 133(9): 1831 - 1844.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
K. E. Whitlock, K. M. Smith, H. Kim, and M. V. Harden
A role for foxd3 and sox10 in the differentiation of gonadotropin-releasing hormone (GnRH) cells in the zebrafish Danio rerio
Development, December 15, 2005; 132(24): 5491 - 5502.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
A. Picker and M. Brand
Fgf signals from a novel signaling center determine axial patterning of the prospective neural retina
Development, November 15, 2005; 132(22): 4951 - 4962.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
F. P. O'Hara, E. Beck, L. K. Barr, L. L. Wong, D. S. Kessler, and R. D. Riddle
Zebrafish Lmx1b.1 and Lmx1b.2 are required for maintenance of the isthmic organizer
Development, July 15, 2005; 132(14): 3163 - 3173.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
T. Xiao, T. Roeser, W. Staub, and H. Baier
A GFP-based genetic screen reveals mutations that disrupt the architecture of the zebrafish retinotectal projection
Development, July 1, 2005; 132(13): 2955 - 2967.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
L. M. Zeltser
Shh-dependent formation of the ZLI is opposed by signals from the dorsal diencephalon
Development, May 1, 2005; 132(9): 2023 - 2033.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 2003