|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Molecular & Cellular Proteomics 5:824-834, 2006.
© 2006 by The American Society for Biochemistry and Molecular Biology, Inc.


From the Department of Biochemistry and Cell Biology, Rice University, Houston, Texas 77005
Positional information provided by Hox homeotic transcription factors is integrated with other transcription factors and cell signaling cascades in specific combinations to dictate context- and gene-specific Hox activity. Protein-protein interactions between these groups have long been hypothesized to modulate Hox functions, yielding a context-specific function. However, difficulties in applying interaction screens to potent transcription factors have limited partner identification. A yeast two-hybrid screen using transcription activation-deficient mutants of the Drosophila melanogaster Hox protein Ultrabithorax IB identified an array of interacting proteins, consisting primarily of transcription factors and components of cell signaling pathways. Interactions were confirmed with wild-type Ultrabithorax (UBX) in phage display experiments and by immunoprecipitation for a subset of partners. In vivo assays demonstrated that two Ultrabithorax IB partners, Armadillo, regulated by Wingless/WNT signaling, and the homeodomain protein Aristaless, inhibit UBX-dependent haltere development from the default wing development pathway. Therefore, transcription factors and cell signaling proteins that subdivide Hox-specified tissues can both alter Hox function in vivo and interact with the corresponding Hox protein in vitro. UBX may also modulate partner function: the pupal death phenotype induced by ectopic expression of the UBX partner Hairy required the presence of UBX. Thus, Hox·transcription factor complexes may integrate a variety of positional cues, generating the specificity and versatility required for context-dependent Hox function.
To whom correspondence should be addressed: Dept. of Biochemistry and Cell Biology, MS140, Rice University, 6100 S. Main St., Houston, TX 77005. Tel.: 713-348-4936; Fax: 713-348-6149; E-mail: bondos{at}rice.edu
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
This article has been cited by other articles:
![]() |
S. Plaza, F. Prince, Y. Adachi, C. Punzo, D. L. Cribbs, and W. J. Gehring Cross-regulatory protein-protein interactions between Hox and Pax transcription factors PNAS, September 9, 2008; 105(36): 13439 - 13444. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Liu, K. S. Matthews, and S. E. Bondos Multiple Intrinsically Disordered Sequences Alter DNA Binding by the Homeodomain of the Drosophila Hox Protein Ultrabithorax J. Biol. Chem., July 25, 2008; 283(30): 20874 - 20887. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Shen, J. Zhang, X. Luo, W. Zhu, K. Yu, K. Chen, Y. Li, and H. Jiang Predicting protein-protein interactions based only on sequences information PNAS, March 13, 2007; 104(11): 4337 - 4341. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Bondos Variations on a Theme: Hox and Wnt Combinatorial Regulation During Animal Development Sci. Signal., October 3, 2006; 2006(355): pe38 - pe38. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| All ASBMB Journals | Journal of Biological Chemistry |
| Journal of Lipid Research | ASBMB Today |