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 21 July 2004
doi: 10.1242/dev.01277


Development 131, 3991-4000 (2004)
Published by The Company of Biologists 2004


This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
dev.01277v1
131/16/3991    most recent
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 Ramel, M.-C.
Right arrow Articles by Lekven, A. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ramel, M.-C.
Right arrow Articles by Lekven, A. C.
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?

Repression of the vertebrate organizer by Wnt8 is mediated by Vent and Vox

Marie-Christine Ramel and Arne C. Lekven*

Department of Biology, Texas A&M University, College Station, TX 77843-3258, USA

* Author for correspondence (e-mail: alekven{at}mail.bio.tamu.edu)

Accepted 12 May 2004

Dorsoventral (DV) patterning of vertebrate embryos requires the concerted action of the Bone Morphogenetic Protein (BMP) and Wnt signaling pathways. In contrast to our understanding of the role of BMP in establishing ventral fates, our understanding of the role of Wnts in ventralizing embryos is less complete. Wnt8 is required for ventral patterning in both Xenopus and zebrafish; however, its mechanism of action remains unclear. We have used the zebrafish to address the requirement for Wnt8 in restricting the size of the dorsal organizer. Epistasis experiments suggest that Wnt8 achieves this restriction by regulating the early expression of the transcriptional repressors Vent and Vox. Our data show that vent and vox are direct transcriptional targets of Wnt8/ß-catenin. Additionally, we show that Wnt8 and Bmp2b co-regulate vent and vox in a dynamic fashion. Thus, whereas both Wnt8 and zygotic BMP are ventralizing agents that regulate common target genes, their temporally different modes of action are necessary to pattern the embryo harmoniously along its DV axis.

Key words: Wnt8, BMP, Dorsoventral, Vent, Vox


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?


This article has been cited by other articles:


Home page
DevelopmentHome page
M. Dixon Fox and A. E. E. Bruce
Short- and long-range functions of Goosecoid in zebrafish axis formation are independent of Chordin, Noggin 1 and Follistatin-like 1b
Development, May 15, 2009; 136(10): 1675 - 1685.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
N.-G. Kim, C. Xu, and B. M. Gumbiner
Identification of targets of the Wnt pathway destruction complex in addition to {beta}-catenin
PNAS, March 31, 2009; 106(13): 5165 - 5170.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
C. Patthey, T. Edlund, and L. Gunhaga
Wnt-regulated temporal control of BMP exposure directs the choice between neural plate border and epidermal fate
Development, January 1, 2009; 136(1): 73 - 83.
[Abstract] [Full Text] [PDF]


Home page
JCBHome page
X.-q. Gan, J.-y. Wang, Y. Xi, Z.-l. Wu, Y.-p. Li, and L. Li
Nuclear Dvl, c-Jun, {beta}-catenin, and TCF form a complex leading to stabiLization of {beta}-catenin-TCF interaction
J. Cell Biol., March 24, 2008; 180(6): 1087 - 1100.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
V. A. McLin, S. A. Rankin, and A. M. Zorn
Repression of Wnt/{beta}-catenin signaling in the anterior endoderm is essential for liver and pancreas development
Development, June 15, 2007; 134(12): 2207 - 2217.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
M. K. Nyholm, S.-F. Wu, R. I. Dorsky, and Y. Grinblat
The zebrafish zic2a-zic5 gene pair acts downstream of canonical Wnt signaling to control cell proliferation in the developing tectum
Development, February 15, 2007; 134(4): 735 - 746.
[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
DevelopmentHome page
U. J. Pyati, M. S. Cooper, A. J. Davidson, A. Nechiporuk, and D. Kimelman
Sustained Bmp signaling is essential for cloaca development in zebrafish
Development, June 1, 2006; 133(11): 2275 - 2284.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
G. Bellipanni, M. Varga, S. Maegawa, Y. Imai, C. Kelly, A. P. Myers, F. Chu, W. S. Talbot, and E. S. Weinberg
Essential and opposing roles of zebrafish {beta}-catenins in the formation of dorsal axial structures and neurectoderm
Development, April 1, 2006; 133(7): 1299 - 1309.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
U. J. Pyati, A. E. Webb, and D. Kimelman
Transgenic zebrafish reveal stage-specific roles for Bmp signaling in ventral and posterior mesoderm development
Development, May 15, 2005; 132(10): 2333 - 2343.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
R. DasGupta, A. Kaykas, R. T. Moon, and N. Perrimon
Functional Genomic Analysis of the Wnt-Wingless Signaling Pathway
Science, May 6, 2005; 308(5723): 826 - 833.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 2004