|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
1 Department of Cell Biology, Vanderbilt University School of Medicine, 1161 21st Avenue South, Nashville, TN 37232-2175, USA
2 Department of Biological Sciences, Vanderbilt University, VU Station B 351634, Nashville, TN 37235, USA
*Authors for correspondence (e-mail: lilianna.solnica-krezel{at}vanderbilt.edu and wrightc{at}ctrvax.vanderbilt.edu)
Accepted June 20, 2001
The dorsal ectoderm of the vertebrate gastrula was proposed by Nieuwkoop to be specified towards an anterior neural fate by an activation signal, with its subsequent regionalization along the anteroposterior (AP) axis regulated by a graded transforming activity, leading to a properly patterned forebrain, midbrain, hindbrain and spinal cord. The activation phase involves inhibition of BMP signals by dorsal antagonists, but the later caudalization process is much more poorly characterized. Explant and overexpression studies in chick, Xenopus, mouse and zebrafish implicate lateral/paraxial mesoderm in supplying the transforming influence, which is largely speculated to be a Wnt family member.
We have analyzed the requirement for the specific ventrolaterally expressed Wnt8 ligand in the posteriorization of neural tissue in zebrafish wild-type and Nodal-deficient embryos (Antivin overexpressing or cyclops;squint double mutants), which show extensive AP brain patterning in the absence of dorsal mesoderm. In different genetic situations that vary the extent of mesodermal precursor formation, the presence of lateral wnt8-expressing cells correlates with the establishment of AP brain pattern. Cell tracing experiments show that the neuroectoderm of Nodal-deficient embryos undergoes a rapid anterior-to-posterior transformation in vivo during a short period at the end of the gastrula stage. Moreover, in both wild-type and Nodal-deficient embryos, inactivation of Wnt8 function by morpholino (MOwnt8) translational interference dose-dependently abrogates formation of spinal cord and posterior brain fates, without blocking ventrolateral mesoderm formation. MOwnt8 also suppresses the forebrain deficiency in bozozok mutants, in which inactivation of a homeobox gene causes ectopic wnt8 expression. In addition, the bozozok forebrain reduction is suppressed in bozozok;squint;cyclops triple mutants, and is associated with reduced wnt8 expression, as seen in cyclops;squint mutants. Hence, whereas boz and Nodal signaling largely cooperate in gastrula organizer formation, they have opposing roles in regulating wnt8 expression and forebrain specification. Our findings provide strong support for a model of neural transformation in which a planar gastrula-stage Wnt8 signal, promoted by Nodal signaling and dorsally limited by Bozozok, acts on anterior neuroectoderm from the lateral mesoderm to produce the AP regional patterning of the CNS.
Key words: Zebrafish, cyclops, squint, bozozok, wnt8, Neuroectoderm, nodal, Morpholino
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati
Twitter What's this?
This article has been cited by other articles:
![]() |
N.-E. Szabo, T. Zhao, M. Cankaya, T. Theil, X. Zhou, and G. Alvarez-Bolado Role of Neuroepithelial Sonic hedgehog in Hypothalamic Patterning J. Neurosci., May 27, 2009; 29(21): 6989 - 7002. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Ding, Y. Xi, T. Chen, J.-y. Wang, D.-l. Tao, Z.-L. Wu, Y.-p. Li, C. Li, R. Zeng, and L. Li Caprin-2 enhances canonical Wnt signaling through regulating LRP5/6 phosphorylation J. Cell Biol., September 8, 2008; 182(5): 865 - 872. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Gaulden and J. F. Reiter Neur-ons and neur-offs: regulators of neural induction in vertebrate embryos and embryonic stem cells Hum. Mol. Genet., April 15, 2008; 17(R1): R60 - R66. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Davidson, B. Mao, I. del Barco Barrantes, and C. Niehrs Kremen proteins interact with Dickkopf1 to regulate anteroposterior CNS patterning Development, March 14, 2003; 129(24): 5587 - 5596. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Grandel, K. Lun, G.-J. Rauch, M. Rhinn, T. Piotrowski, C. Houart, P. Sordino, A. M. Kuchler, S. Schulte-Merker, R. Geisler, et al. Retinoic acid signalling in the zebrafish embryo is necessary during pre-segmentation stages to pattern the anterior-posterior axis of the CNS and to induce a pectoral fin bud Development, March 8, 2003; 129(12): 2851 - 2865. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Take-uchi, J. D. W. Clarke, and S. W. Wilson Hedgehog signalling maintains the optic stalk-retinal interface through the regulation of Vax gene activity Development, March 1, 2003; 130(5): 955 - 968. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. W. Houston, M. Kofron, E. Resnik, R. Langland, O. Destree, C. Wylie, and J. Heasman Repression of organizer genes in dorsal and ventral Xenopus cells mediated by maternal XTcf3 Development, September 1, 2002; 129(17): 4015 - 4025. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. B. Xanthos, M. Kofron, Q. Tao, K. Schaible, C. Wylie, and J. Heasman The roles of three signaling pathways in the formation and function of the Spemann Organizer Development, September 1, 2002; 129(17): 4027 - 4043. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. C. Yelick and T. F. Schilling MOLECULAR DISSECTION OF CRANIOFACIAL DEVELOPMENT USING ZEBRAFISH Critical Reviews in Oral Biology & Medicine, July 1, 2002; 13(4): 308 - 322. [Abstract] [Full Text] [PDF] |
||||