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    

doi: 10.1242/10.1242/dev.00409


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 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 Gross, J. M.
Right arrow Articles by McClay, D. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gross, J. M.
Right arrow Articles by McClay, D. R.
Development 130, 1989-1999 (2003)
Copyright © 2003 The Company of Biologists Limited

LvTbx2/3: a T-box family transcription factor involved in formation of the oral/aboral axis of the sea urchin embryo

Jeffrey M. Gross*, Robert E. Peterson, Shu-Yu Wu and David R. McClay{dagger}

Development, Cell and Molecular Biology Group, Box 91000 LSRC, Duke University, Durham, NC 27710, USA
* Present address: Department of Molecular and Cellular Biology, Harvard University, BioLabs 2094, Cambridge, MA 02138, USA

{dagger} Author for correspondence (e-mail: david.mcclay{at}duke.edu)

Accepted 13 December 2002

T-box family transcription factors have been identified in many organisms and are frequently associated with patterning events during embryonic development. With an interest in the molecular basis of patterning in the sea urchin embryo, we identified several members of the T-box family in Lytechinus variegatus. Here, we report the cloning and characterization of an ortholog of the Tbx2/3 subfamily, LvTbx2/3. To characterize the spatial distribution of LvTbx2/3 protein throughout sea urchin embryogenesis, a polyclonal antiserum was generated. Nuclear localization of LvTbx2/3 initiated at the mesenchyme blastula stage and protein was present into the pluteus stage. Localization was asymmetric throughout this period and costaining with marker genes indicated that asymmetry was about the oral/aboral (O/A) axis. Asymmetric distribution of LvTbx2/3 was observed in the aboral territories of all three germ layers. In the skeletogenic mesoderm lineage, LvTbx2/3 expression was dynamic because expression appeared initially in all skeletogenic mesenchyme cells (PMCs) but, subsequently, became refined solely to the aboral ones during skeletogenesis. To determine if the aboral expression of LvTbx2/3 is linked between germ layers, and to place LvTbx2/3 in the sequence of events that specifies the O/A axis, the effects of a series of perturbations to O/A polarity on LvTbx2/3 expression in each germ layer were examined. Preventing the nuclear localization of ß-catenin, pharmacological disruption of the O/A axis with NiCl2, overexpression of BMP2/4 and disruption of the extracellular matrix all blocked LvTbx2/3 expression in all germ layers. This indicates that expression of LvTbx2/3 in the aboral territories of each germ layer is a common aspect of O/A specification, downstream of the molecular events that specify the axis. Furthermore, blocking the nuclear localization of ß-catenin, overexpression of BMP2/4 and disruption of the extracellular matrix also prevented the oral (stomodael) expression of LvBrachyury (LvBrac) protein, indicating that the O/A axis is established by a complex series of events. Last, the function of LvTbx2/3 in the formation of the O/A axis was characterized by examining the phenotypic consequences of ectopic expression of LvTbx2/3 mRNA on embryonic development and the expression of marker genes that identify specific germ layers and tissues. Ectopic expression of LvTbx2/3 produced profound morphogenetic defects in derivatives of each germ layer with no apparent loss in specification events in those tissues. This indicates that LvTbx2/3 functions as a regulator of morphogenetic movements in the aboral compartments of the ectoderm, endoderm and mesoderm.

Key words: Sea urchin, T-box, Tbx2/3, Oral/aboral, Morphogenesis




This article has been cited by other articles:


Home page
DevelopmentHome page
L. Duloquin, G. Lhomond, and C. Gache
Localized VEGF signaling from ectoderm to mesenchyme cells controls morphogenesis of the sea urchin embryo skeleton
Development, June 15, 2007; 134(12): 2293 - 2302.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
S.-Y. Wu and D. R. McClay
The Snail repressor is required for PMC ingression in the sea urchin embryo
Development, March 15, 2007; 134(6): 1061 - 1070.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
C.-A. Renard, C. Labalette, C. Armengol, D. Cougot, Y. Wei, S. Cairo, P. Pineau, C. Neuveut, A. de Reynies, A. Dejean, et al.
Tbx3 Is a Downstream Target of the Wnt/{beta}-Catenin Pathway and a Critical Mediator of {beta}-Catenin Survival Functions in Liver Cancer
Cancer Res., February 1, 2007; 67(3): 901 - 910.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
J. Croce, L. Duloquin, G. Lhomond, D. R. McClay, and C. Gache
Frizzled5/8 is required in secondary mesenchyme cells to initiate archenteron invagination during sea urchin development
Development, February 1, 2006; 133(3): 547 - 557.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
C. A. Bradham and D. R. McClay
p38 MAPK is essential for secondary axis specification and patterning in sea urchin embryos
Development, January 1, 2006; 133(1): 21 - 32.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 2003