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 August 18, 2003
doi: 10.1242/10.1242/dev.00684


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 Shimmi, O.
Right arrow Articles by O'Connor, M. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Shimmi, O.
Right arrow Articles by O'Connor, M. B.
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?
Development 130, 4673-4682 (2003)
Copyright © 2003 The Company of Biologists Limited

Physical properties of Tld, Sog, Tsg and Dpp protein interactions are predicted to help create a sharp boundary in Bmp signals during dorsoventral patterning of the Drosophila embryo

Osamu Shimmi and Michael B. O'Connor*

Department of Genetics, Cell Biology and Development, Howard Hughes Medical Institute, University of Minnesota, Minneapolis, MN 55455, USA

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

Accepted 23 June 2003

Dorsal cell fate in Drosophila embryos is specified by an activity gradient of Decapentaplegic (Dpp), a homologue of bone morphogenetic proteins (Bmps) 2/4. Previous genetic and biochemical studies have revealed that the Sog, Tsg and Tld proteins modify Dpp activity at the post-transcriptional level. The predominant view is that Sog and Tsg form a strong ternary complex with Dpp that prevents it from binding to its cognate receptors in lateral regions of the embryo, while in the dorsalmost cells Tld is proposed to process Sog and thereby liberate Dpp for signaling. In this model, it is not readily apparent how Tld activity is restricted to the dorsal-most cells as it is expressed throughout the entire dorsal domain. In this study, additional genetic and biochemical assays were developed to further probe the relationships between the Sog, Tsg, Tld and Dpp proteins. Using cell based assays, we find that the dynamic range over which Dpp functions for signaling is the same range in which Dpp stimulates the cleavage of Sog by Tld. In addition, our data supports a role for Tsg in sensitizing the patterning mechanism to low levels of Dpp. We propose that the strong Dpp concentration dependence exhibited by the processing reaction, together with movement of Dpp by Sog and Tsg protein can help explain how Tld activity is confined to the dorsal-most region of the embryo through formation of a spatially dependent positive and negative reinforcement loop. Such a mechanism also explains how a sharp rather than smooth signaling boundary is formed.

Key words: Tld, Dpp, Morphogen, Bmp


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
Proc. Natl. Acad. Sci. USAHome page
J. Kunnapuu, I. Bjorkgren, and O. Shimmi
The Drosophila DPP signal is produced by cleavage of its proprotein at evolutionary diversified furin-recognition sites
PNAS, May 26, 2009; 106(21): 8501 - 8506.
[Abstract] [Full Text] [PDF]


Home page
J R Soc InterfaceHome page
D. M Umulis
Analysis of dynamic morphogen scale invariance
J R Soc Interface, March 11, 2009; (2009) rsif.2009.0015v1.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
T. J. Geach and L. Dale
Molecular Determinants of Xolloid Action in Vivo
J. Biol. Chem., October 3, 2008; 283(40): 27057 - 27063.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
M. Serpe and M. B. O'Connor
The metalloprotease Tolloid-related and its TGF-{beta}-like substrate Dawdle regulate Drosophila motoneuron axon guidance.
Development, December 1, 2006; 133(24): 4969 - 4979.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
D. M. Umulis, M. Serpe, M. B. O'Connor, and H. G. Othmer
Robust, bistable patterning of the dorsal surface of the Drosophila embryo
PNAS, August 1, 2006; 103(31): 11613 - 11618.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
J. Lin, S. R. Patel, M. Wang, and G. R. Dressler
The Cysteine-Rich Domain Protein KCP Is a Suppressor of Transforming Growth Factor {beta}/Activin Signaling in Renal Epithelia
Mol. Cell. Biol., June 15, 2006; 26(12): 4577 - 4585.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
E. G. Canty, L. Garrigue-Antar, and K. E. Kadler
A Complete Domain Structure of Drosophila Tolloid Is Required for Cleavage of Short Gastrulation
J. Biol. Chem., May 12, 2006; 281(19): 13258 - 13267.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
F. Rentzsch, J. Zhang, C. Kramer, W. Sebald, and M. Hammerschmidt
Crossveinless 2 is an essential positive feedback regulator of Bmp signaling during zebrafish gastrulation
Development, March 1, 2006; 133(5): 801 - 811.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
M. B. O'Connor, D. Umulis, H. G. Othmer, and S. S. Blair
Shaping BMP morphogen gradients in the Drosophila embryo and pupal wing
Development, January 15, 2006; 133(2): 183 - 193.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
M. Serpe, A. Ralston, S. S. Blair, and M. B. O'Connor
Matching catalytic activity to developmental function: Tolloid-related processes Sog in order to help specify the posterior crossvein in the Drosophila wing
Development, June 1, 2005; 132(11): 2645 - 2656.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
M. Xu, N. Kirov, and C. Rushlow
Peak levels of BMP in the Drosophila embryo control target genes by a feed-forward mechanism
Development, April 1, 2005; 132(7): 1637 - 1647.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
J. Xie and S. Fisher
Twisted gastrulation enhances BMP signaling through chordin dependent and independent mechanisms
Development, January 15, 2005; 132(2): 383 - 391.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
A. J. Zhu and M. P. Scott
Incredible journey: how do developmental signals travel through tissue?
Genes & Dev., December 15, 2004; 18(24): 2985 - 2997.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
S. C. Little and M. C. Mullins
Twisted gastrulation promotes BMP signaling in zebrafish dorsal-ventral axial patterning
Development, December 1, 2004; 131(23): 5825 - 5835.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
K. Yu, K.-H. Kang, P. Heine, U. Pyati, S. Srinivasan, B. Biehs, D. Kimelman, and E. Bier
Cysteine Repeat Domains and Adjacent Sequences Determine Distinct Bone Morphogenetic Protein Modulatory Activities of the Drosophila Sog Protein
Genetics, March 1, 2004; 166(3): 1323 - 1336.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
L. Zakin and E. M. De Robertis
Inactivation of mouse Twisted gastrulation reveals its role in promoting Bmp4 activity during forebrain development
Development, January 15, 2004; 131(2): 413 - 424.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 2003