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 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 Ahn, K.
Right arrow Articles by Crenshaw, E. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ahn, K.
Right arrow Articles by Crenshaw, E. B., III
Development 128, 4449-4461 (2001)
© 2001 The Company of Biologists Limited

BMPR-IA signaling is required for the formation of the apical ectodermal ridge and dorsal-ventral patterning of the limb

Kyung Ahn1, Yuji Mishina2,3, Mark C. Hanks4, Richard R. Behringer2 and E. Bryan Crenshaw, III1,*

1 Department of Neuroscience, University of Pennsylvania Medical School, Philadelphia, PA, USA
2 Department of Molecular Genetics, University of Texas MD Anderson Cancer Center, Houston, TX, USA
3 Laboratory of Reproductive and Developmental Toxicology, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA
4 Procter & Gamble Pharmaceuticals, Mason, OH, USA

*Author for correspondence (e-mail: crenshab{at}mail.med.upenn.edu)

Accepted August 21, 2001

We demonstrate that signaling via the bone morphogenetic protein receptor IA (BMPR-IA) is required to establish two of the three cardinal axes of the limb: the proximal-distal axis and the dorsal-ventral axis. We generated a conditional knockout of the gene encoding BMPR-IA (Bmpr) that disrupted BMP signaling in the limb ectoderm. In the most severely affected embryos, this conditional mutation resulted in gross malformations of the limbs with complete agenesis of the hindlimbs. The proximal-distal axis is specified by the apical ectodermal ridge (AER), which forms from limb ectoderm at the distal tip of the embryonic limb bud. Analyses of the expression of molecular markers, such as Fgf8, demonstrate that formation of the AER was disrupted in the Bmpr mutants. Along the dorsal/ventral axis, loss of engrailed 1 (En1) expression in the non-ridge ectoderm of the mutants resulted in a dorsal transformation of the ventral limb structures. The expression pattern of Bmp4 and Bmp7 suggest that these growth factors play an instructive role in specifying dorsoventral pattern in the limb. This study demonstrates that BMPR-IA signaling plays a crucial role in AER formation and in the establishment of the dorsal/ventral patterning during limb development.

Key words: Apical ectodermal ridge, Bone morphogenetic protein receptor, Dorsal-ventral patterning, Engrailed 1, Limb development, loxP/cre conditional knockout, Mouse




This article has been cited by other articles:


Home page
DevelopmentHome page
C. Liu, E. Nakamura, V. Knezevic, S. Hunter, K. Thompson, and S. Mackem
A role for the mesenchymal T-box gene Brachyury in AER formation during limb development
Development, April 1, 2003; 130(7): 1327 - 1337.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
Y. Liu, C. Liu, Y. Yamada, and C.-M. Fan
growth arrest specific gene 1 acts as a region-specific mediator of the Fgf10/Fgf8 regulatory loop in the limb
Development, March 13, 2003; 129(22): 5289 - 5300.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
T. L. Belecky-Adams, R. Adler, and D. C. Beebe
Bone morphogenetic protein signaling and the initiation of lens fiber cell differentiation
Development, March 10, 2003; 129(16): 3795 - 3802.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
J. R. Barrow, K. R. Thomas, O. Boussadia-Zahui, R. Moore, R. Kemler, M. R. Capecchi, and A. P. McMahon
Ectodermal Wnt3/beta -catenin signaling is required for the establishment and maintenance of the apical ectodermal ridge
Genes & Dev., February 1, 2003; 17(3): 394 - 409.
[Abstract] [Full Text] [PDF]


Home page
Endocr. Rev.Home page
H. Chang, C. W. Brown, and M. M. Matzuk
Genetic Analysis of the Mammalian Transforming Growth Factor-{beta} Superfamily
Endocr. Rev., December 1, 2002; 23(6): 787 - 823.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
V. Gaussin, T. Van de Putte, Y. Mishina, M. C. Hanks, A. Zwijsen, D. Huylebroeck, R. R. Behringer, and M. D. Schneider
Endocardial cushion and myocardial defects after cardiac myocyte-specific conditional deletion of the bone morphogenetic protein receptor ALK3
PNAS, February 14, 2002; (2002) 42390499.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
S. Pizette, C. Abate-Shen, and L. Niswander
BMP controls proximodistal outgrowth, via induction of the apical ectodermal ridge, and dorsoventral patterning in the vertebrate limb
Development, November 15, 2001; 128(22): 4463 - 4474.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
V. Gaussin, T. Van de Putte, Y. Mishina, M. C. Hanks, A. Zwijsen, D. Huylebroeck, R. R. Behringer, and M. D. Schneider
Endocardial cushion and myocardial defects after cardiac myocyte-specific conditional deletion of the bone morphogenetic protein receptor ALK3
PNAS, March 5, 2002; 99(5): 2878 - 2883.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 2001