Genetics, Vol 135, 1047-1062, Copyright © 1993


INVESTIGATIONS

Segmental Polarity in Drosophila melanogaster: Genetic Dissection of fused in a Suppressor of fused Background Reveals Interaction With costal-2

T. Preat, P. Therond, B. Limbourg-Bouchon, A. Pham, H. Tricoire, D. Busson and C. Lamour-Isnard
Present address: Institut Alfred Fessard, C.N.R.S. 91198 Gif-sur-Yvette Cedex, France.

fused (fu) is a segment polarity gene that encodes a putative serine/threonine kinase. A complete suppressor of the embryonic and adult phenotypes of fu mutants, Suppressor of fused (Su(fu)), was previously described. The amorphic Su(fu) mutation is viable and displays no phenotype by itself. We have used this suppressor as a tool to perform a genetic dissection of the fu gene. Analysis of the interaction between Su(fu) and 33 fu alleles shows that they belong to three different classes. Defects due to class I fu alleles are fully suppressed by Su(fu). Class II fu alleles lead to a new segment polarity phenotype in interaction with Su(fu). This phenotype corresponds to embryonic and adult anomalies similar to those displayed by the segment polarity mutant costal-2 (cos-2). Class II alleles are recessive to class I alleles in a fu[I]/fu[II];Su(fu)/Su(fu) combination. Class 0 alleles, like class I alleles, confer a normal segmentation phenotype in interaction with Su(fu). However class II alleles are dominant over class 0 alleles in a fu[0]/fu[II];Su(fu)/Su(fu) combination. Alleles of class I and II correspond to small molecular events, which may leave part of the Fu protein intact. On the contrary, class 0 alleles correspond to large deletions. Several class I and class II fu mutations have been mapped, and three mutant alleles were sequenced. These data suggest that class I mutations affect the catalytic domain of the putative Fu kinase and leave the carboxy terminal domain intact, whereas predicted class II proteins have an abnormal carboxy terminal domain. Su(fu) enhances the cos-2 phenotype and cos-2 mutations interact with fu in a way similar to Su(fu). All together these results suggest that a close relationship might exist between fu, Su(fu) and cos-2 throughout development. We thus propose a model where the Fu(+) kinase is a posterior inhibitor of Costal-2(+) while Su(fu)(+) is an activator of Costal-2(+). The expression pattern of wingless and engrailed in fu and fu;Su(fu) embryos is in accordance with this interpretation.


This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
S. F. Farzan, M. A. Stegman, S. K. Ogden, M. Ascano Jr, K. E. Black, O. Tacchelly, and D. J. Robbins
A Quantification of Pathway Components Supports a Novel Model of Hedgehog Signal Transduction
J. Biol. Chem., October 16, 2009; 284(42): 28874 - 28884.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
M.-H. Chen, C. W. Wilson, Y.-J. Li, K. K. L. Law, C.-S. Lu, R. Gacayan, X. Zhang, C.-c. Hui, and P.-T. Chuang
Cilium-independent regulation of Gli protein function by Sufu in Hedgehog signaling is evolutionarily conserved
Genes & Dev., August 15, 2009; 23(16): 1910 - 1928.
[Abstract] [Full Text] [PDF]


Home page
Sci SignalHome page
M. Evangelista, T. Y. Lim, J. Lee, L. Parker, A. Ashique, A. S. Peterson, W. Ye, D. P. Davis, and F. J. de Sauvage
Kinome siRNA Screen Identifies Regulators of Ciliogenesis and Hedgehog Signal Transduction
Sci. Signal., September 30, 2008; 1(39): ra7 - ra7.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
Y. Liu, X. Cao, J. Jiang, and J. Jia
Fused Costal2 protein complex regulates Hedgehog-induced Smo phosphorylation and cell-surface accumulation
Genes & Dev., August 1, 2007; 21(15): 1949 - 1963.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
M.-H. Chen, N. Gao, T. Kawakami, and P.-T. Chuang
Mice Deficient in the Fused Homolog Do Not Exhibit Phenotypes Indicative of Perturbed Hedgehog Signaling during Embryonic Development
Mol. Cell. Biol., August 15, 2005; 25(16): 7042 - 7053.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
M. Merchant, M. Evangelista, S.-M. Luoh, G. D. Frantz, S. Chalasani, R. A. D. Carano, M. van Hoy, J. Ramirez, A. K. Ogasawara, L. M. McFarland, et al.
Loss of the Serine/Threonine Kinase Fused Results in Postnatal Growth Defects and Lethality Due to Progressive Hydrocephalus
Mol. Cell. Biol., August 15, 2005; 25(16): 7054 - 7068.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
M. Ascano Jr. and D. J. Robbins
An Intramolecular Association between Two Domains of the Protein Kinase Fused Is Necessary for Hedgehog Signaling
Mol. Cell. Biol., December 1, 2004; 24(23): 10397 - 10405.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
J. I. Horabin, S. Walthall, C. Vied, and M. Moses
A positive role for Patched in Hedgehog signaling revealed by the intracellular trafficking of Sex-lethal, the Drosophila sex determination master switch
Development, December 15, 2003; 130(24): 6101 - 6109.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
F. Besse, D. Busson, and A.-M. Pret
Fused-dependent Hedgehog signal transduction is required for somatic cell differentiation during Drosophila egg chamber formation
Development, September 1, 2002; 129(17): 4111 - 4124.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
M. Ascano Jr., K. E. Nybakken, J. Sosinski, M. A. Stegman, and D. J. Robbins
The Carboxyl-Terminal Domain of the Protein Kinase Fused Can Function as a Dominant Inhibitor of Hedgehog Signaling
Mol. Cell. Biol., March 1, 2002; 22(5): 1555 - 1566.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
T. Fukumoto, R. Watanabe-Fukunaga, K. Fujisawa, S. Nagata, and R. Fukunaga
The Fused Protein Kinase Regulates Hedgehog-stimulated Transcriptional Activation in Drosophila Schneider 2 Cells
J. Biol. Chem., October 12, 2001; 276(42): 38441 - 38448.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
N Methot and K Basler
Suppressor of fused opposes hedgehog signal transduction by impeding nuclear accumulation of the activator form of Cubitus interruptus
Development, January 9, 2000; 127(18): 4001 - 4010.
[Abstract] [PDF]


Home page
DevelopmentHome page
Q. Wang and R. Holmgren
Nuclear import of cubitus interruptus is regulated by hedgehog via a mechanism distinct from Ci stabilization and Ci activation
Development, January 7, 2000; 127(14): 3131 - 3139.
[Abstract] [PDF]


Home page
DevelopmentHome page
P. Therond, B Limbourg Bouchon, A Gallet, F Dussilol, T Pietri, M van den Heuvel, and H Tricoire
Differential requirements of the fused kinase for hedgehog signalling in the Drosophila embryo
Development, January 9, 1999; 126(18): 4039 - 4051.
[Abstract] [PDF]


Home page
DevelopmentHome page
A Cernac, C Lincoln, D Lammer, and M Estelle
The SAR1 gene of Arabidopsis acts downstream of the AXR1 gene in auxin response
Development, January 4, 1997; 124(8): 1583 - 1591.
[Abstract] [PDF]


Home page
Cold Spring Harb Symp Quant BiolHome page
R.L. Johnson and M.P. Scott
Control of Cell Growth and Fate by patched Genes
Cold Spring Harb Symp Quant Biol, January 1, 1997; 62(0): 205 - 215.
[Abstract] [PDF]


Home page
J. Biol. Chem.Home page
M. A. Stegman, J. E. Vallance, G. Elangovan, J. Sosinski, Y. Cheng, and D. J. Robbins
Identification of a Tetrameric Hedgehog Signaling Complex
J. Biol. Chem., July 14, 2000; 275(29): 21809 - 21812.
[Abstract] [Full Text] [PDF]