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PMID: 9584131 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Local induction of patterning and programmed cell death in the developing Drosophila retina.

Development (Cambridge, England) ·Vol. 125 ·No. 12 ·1998-06-00 ·Pages 2327-35

Miller DT, Cagan RL

Abstract

Local cell signaling can pattern the nervous system by directing cell fates, including programmed cell death. In the developing Drosophila retina, programmed cell death is used to remove excess cells between ommatidia. Cell ablation revealed the source and position of signals required for regulating the pattern of programmed cell death among these interommatidial cells. Two types of signals regulate this patterning event. Notch-mediated signals between interommatidial precursors result in removal of unneeded cells. Cone cells and primary pigment cells oppose this signal by supplying a 'life'-promoting activity; evidence is provided that this signal occurs through localized activation of the EGF Receptor/Ras pathway. Together, these signals refine the highly regular pattern observed in the adult retina.

MeSH Terms
Animals Apoptosis Body Patterning Drosophila Drosophila Proteins ErbB Receptors/metabolism Membrane Proteins/genetics,physiology Photoreceptor Cells, Invertebrate/cytology,growth & development Protein Kinases Pupa Receptors, Invertebrate Peptide/metabolism Receptors, Notch Retina/cytology,growth & development Signal Transduction ras Proteins/physiology
Chemicals
Drosophila Proteins Membrane Proteins N protein, Drosophila Receptors, Invertebrate Peptide Receptors, Notch Protein Kinases Egfr protein, Drosophila ErbB Receptors ras Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Miller D T
Washington University School of Medicine, Department of Molecular Biology and Pharmacology, Box 8103, St. Louis, MO 63110, USA.
Cagan R L
Article Info
Journal
Development (Cambridge, England)
Abbr.
Development
ISSN
0950-1991
Published
1998-06-00
Pages
2327-35
Language
English
Region
England
NLM ID
8701744
Subset
IM
Grants
NIGMS NIH HHS · 5T32GM07805 · United States
NEI NIH HHS · R01-EY10717 · United States
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