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 Full Text (PDF)
Right arrow References
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 Matsuo, T.
Right arrow Articles by Yamamoto, D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Matsuo, T.
Right arrow Articles by Yamamoto, D.

Development, Vol 124, Issue 14 2671-2680, Copyright © 1997 by Company of Biologists


JOURNAL ARTICLES

Regulation of cone cell formation by Canoe and Ras in the developing Drosophila eye

T Matsuo, K Takahashi, S Kondo, K Kaibuchi and D Yamamoto
Mitsubishi Kasei Institute of Life Sciences, and ERATO Yamamoto Behavior Genes Project, Machida, Tokyo, Japan.

Cone cells are lens-secreting cells in ommatidia, the unit eyes that compose the compound eye of Drosophila. Each ommatidium contains four cone cells derived from precursor cells of the R7 equivalence group which express the gene sevenless (sev). When a constitutively active form of Ras1 (Ras1V12) is expressed in the R7 equivalence group cells using the sev promoter (sev-Ras1V12), additional cone cells are formed in the ommatidium. Expression of Ras1N17, a dominant negative form of Ras1, results in the formation of 1-3 fewer cone cells than normal in the ommatidium. The effects of Ras1 variants on cone cell formation are modulated by changing the gene dosage at the canoe (cno) locus, which encodes a cytoplasmic protein with Ras-binding activity. An increase or decrease in gene dosage potentiates the sev-Ras1v12 action, leading to marked induction of cone cells. A decrease in cno+ activity also enhances the sev-Ras1N17 action, resulting in a further decrease in the number of cone cells contained in the ommatidium. In the absence of expression of sev-Ras1V12 or sev-Ras1N17, an overdose of wild-type cno (cno+) promotes cone cell formation while a significant reduction in cno+ activity results in the formation of 1-3 fewer cone cells than normal in the ommatidium. We propose that there are two signaling pathways in cone cell development, one for its promotion and the other for its repression, and Cno functions as a negative regulator for both pathways. We also postulate that Cno predominantly acts on a prevailing pathway in a given developmental context, thereby resulting in either an increase or a decrease in the number of cone cells per ommatidium. The extra cone cells resulting from the interplay of Ras1v12 and Cno are generated from a pool of undifferentiated cells that are normally fated to develop into pigment cells or undergo apoptosis.


This article has been cited by other articles:


Home page
J. Cell Sci.Home page
M. Sese, M. Corominas, H. Stocker, T. I. Heino, E. Hafen, and F. Serras
The Cdi/TESK1 kinase is required for Sevenless signaling and epithelial organization in the Drosophila eye
J. Cell Sci., December 15, 2006; 119(24): 5047 - 5056.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
A. Brumby, J. Secombe, J. Horsfield, M. Coombe, N. Amin, D. Coates, R. Saint, and H. Richardson
A Genetic Screen for Dominant Modifiers of a cyclin E Hypomorphic Mutation Identifies Novel Regulators of S-Phase Entry in Drosophila
Genetics, September 1, 2004; 168(1): 227 - 251.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
K. Gaengel and M. Mlodzik
Egfr signaling regulates ommatidial rotation and cell motility in the Drosophila eye via MAPK/Pnt signaling and the Ras effector Canoe/AF6
Development, November 15, 2003; 130(22): 5413 - 5423.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
B. Boettner, P. Harjes, S. Ishimaru, M. Heke, H. Q. Fan, Y. Qin, L. Van Aelst, and U. Gaul
The AF-6 Homolog Canoe Acts as a Rap1 Effector During Dorsal Closure of the Drosophila Embryo
Genetics, September 1, 2003; 165(1): 159 - 169.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
G. Radziwill, R. A. Erdmann, U. Margelisch, and K. Moelling
The Bcr Kinase Downregulates Ras Signaling by Phosphorylating AF-6 and Binding to Its PDZ Domain
Mol. Cell. Biol., July 1, 2003; 23(13): 4663 - 4672.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
E. Bergeret, I. Pignot-Paintrand, A. Guichard, K. Raymond, M.-O. Fauvarque, M. Cazemajor, and R. Griffin-Shea
RotundRacGAP Functions with Ras during Spermatogenesis and Retinal Differentiation in Drosophila melanogaster
Mol. Cell. Biol., September 15, 2001; 21(18): 6280 - 6291.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
T. Lukacsovich, Z. Asztalos, W. Awano, K. Baba, S. Kondo, S. Niwa, and D. Yamamoto
Dual-Tagging Gene Trap of Novel Genes in Drosophila melanogaster
Genetics, February 1, 2001; 157(2): 727 - 742.
[Abstract] [Full Text]


Home page
Proc. Natl. Acad. Sci. USAHome page
B. Boettner, E.-E. Govek, J. Cross, and L. Van Aelst
The junctional multidomain protein AF-6 is a binding partner of the Rap1A GTPase and associates with the actin cytoskeletal regulator profilin
PNAS, August 1, 2000; 97(16): 9064 - 9069.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
D. D. Thomas, C. A. Donnelly, R. J. Wood, and L. S. Alphey
Insect Population Control Using a Dominant, Repressible, Lethal Genetic System
Science, March 31, 2000; 287(5462): 2474 - 2476.
[Abstract] [Full Text]


Home page
DevelopmentHome page
A. Cadavid, A Ginzel, and J. Fischer
The function of the Drosophila fat facets deubiquitinating enzyme in limiting photoreceptor cell number is intimately associated with endocytosis
Development, January 4, 2000; 127(8): 1727 - 1736.
[Abstract] [PDF]


Home page
JCBHome page
S. Taya, T. Yamamoto, K. Kano, Y. Kawano, A. Iwamatsu, T. Tsuchiya, K. Tanaka, M. Kanai-Azuma, S. A. Wood, J. S. Mattick, et al.
The Ras Target AF-6 is a Substrate of the Fam Deubiquitinating Enzyme
J. Cell Biol., August 24, 1998; 142(4): 1053 - 1062.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A. B. Vojtek and C. J. Der
Increasing Complexity of the Ras Signaling Pathway
J. Biol. Chem., August 7, 1998; 273(32): 19925 - 19928.
[Full Text] [PDF]


Home page
DevelopmentHome page
D. Miller and R. Cagan
Local induction of patterning and programmed cell death in the developing Drosophila retina
Development, January 6, 1998; 125(12): 2327 - 2335.
[Abstract] [PDF]


Home page
JCBHome page
T. Yamamoto, N. Harada, K. Kano, S.-i. Taya, E. Canaani, Y. Matsuura, A. Mizoguchi, C. Ide, and K. Kaibuchi
The Ras Target AF-6 Interacts with ZO-1 and Serves as a Peripheral Component of Tight Junctions in Epithelial Cells
J. Cell Biol., November 3, 1997; 139(3): 785 - 795.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 1997