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 Irving, C.
Right arrow Articles by Mason, I.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Irving, C.
Right arrow Articles by Mason, I.

Development, Vol 126, Issue 18 3981-3989, Copyright © 1999 by Company of Biologists


JOURNAL ARTICLES

Regeneration of isthmic tissue is the result of a specific and direct interaction between rhombomere 1 and midbrain

C Irving and I Mason
MRC Brain Development Programme, Department of Developmental Neurobiology, Guy's, King's and St. Thomas' Hospital Medical School, Hodgkin Building, Guy's Campus, London SE1 9RT, UK.

The midbrain-hindbrain boundary, or isthmus, is the source of signals that are responsible for regional specification of both the midbrain and anterior hindbrain. Fibroblast growth factor 8 (Fgf8) is expressed specifically at the isthmus and there is now good evidence that it forms at least part of the patterning signal. In this study, we use Fgf8 as a marker for isthmic cells to examine how interactions between midbrain and hindbrain can regenerate isthmic tissue and, thereby, gain insight into the normal formation and/or maintenance of the isthmus. We show that Fgf8-expressing tissue with properties of the isthmic organiser is generated when midbrain and rhombomere 1 tissue are juxtaposed but not when midbrain contacts any other rhombomere. The use of chick/quail chimeras shows that the isthmic tissue is largely derived from rhombomere 1. In a few cases a small proportion of the Fgf8-positive cells were of midbrain origin but this appears to be the result of a local respecification to a hindbrain phenotype, a process mimicked by ectopic FGF8. Studies in vitro show that the induction of Fgf8 is the result of a direct planar interaction between the two tissues and involves a diffusible signal.


This article has been cited by other articles:


Home page
J. Neurosci.Home page
R. W. Koster and S. E. Fraser
FGF signaling mediates regeneration of the differentiating cerebellum through repatterning of the anterior hindbrain and reinitiation of neuronal migration.
J. Neurosci., July 5, 2006; 26(27): 7293 - 7304.
[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
A. Liu, J. Y. H. Li, C. Bromleigh, Z. Lao, L. A. Niswander, and A. L. Joyner
FGF17b and FGF18 have different midbrain regulatory properties from FGF8b or activated FGF receptors
Development, December 22, 2003; 130(25): 6175 - 6185.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
J. Walshe and I. Mason
Unique and combinatorial functions of Fgf3 and Fgf8 during zebrafish forebrain development
Development, September 15, 2003; 130(18): 4337 - 4349.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
S. Agarwala and C. W. Ragsdale
A role for midbrain arcs in nucleogenesis
Development, March 14, 2003; 129(24): 5779 - 5788.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
E. Matsunaga, T. Katahira, and H. Nakamura
Role of Lmx1b and Wnt1 in mesencephalon and metencephalon development
Development, March 13, 2003; 129(22): 5269 - 5277.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
C. Irving, A. Malhas, S. Guthrie, and I. Mason
Establishing the trochlear motor axon trajectory: role of the isthmic organiser and Fgf8
Development, January 12, 2002; 129(23): 5389 - 5398.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
J. Y. H. Li and A. L. Joyner
Otx2 and Gbx2 are required for refinement and not induction of mid-hindbrain gene expression
Development, December 15, 2001; 128(24): 4979 - 4991.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
H.-G. Belting, G. Hauptmann, D. Meyer, S. Abdelilah-Seyfried, A. Chitnis, C. Eschbach, I. Soll, C. Thisse, B. Thisse, K. B. Artinger, et al.
spiel ohne grenzen/pou2 is required during establishment of the zebrafish midbrain-hindbrain boundary organizer
Development, November 1, 2001; 128(21): 4165 - 4176.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
Y Tashiro, M Miyahara, R Shirasaki, M Okabe, C. Heizmann, and F Murakami
Local nonpermissive and oriented permissive cues guide vestibular axons to the cerebellum
Development, January 3, 2001; 128(6): 973 - 981.
[Abstract] [PDF]


Home page
DevelopmentHome page
C Irving and I Mason
Signalling by FGF8 from the isthmus patterns anterior hindbrain and establishes the anterior limit of Hox gene expression
Development, January 1, 2000; 127(1): 177 - 186.
[Abstract] [PDF]




© The Company of Biologists Ltd 1999