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Developmental Dynamics
Article . 2010 . Peer-reviewed
License: Wiley Online Library User Agreement
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Canonical wingless signaling regulates cone cell specification in the Drosophila retina

Authors: Ross L. Cagan; Julia B. Cordero;

Canonical wingless signaling regulates cone cell specification in the Drosophila retina

Abstract

AbstractCorrect tissue patterning during development involves multiple morphogenetic events that include specification of different cell fates, cell proliferation, cell death, and coordinated changes in cell shape, position, and adhesion. Here, we use the Drosophila retina to explore the molecular mechanisms that regulate and integrate these various events. In a previous report, we found that wingless (wg) was required to induce a previously unknown surge of cell death (“early death”) in the pupal retina. Here, we show that wg is also required to induce the more widely studied mid‐pupal cell death (“late death”) in a process that involves regulation of DIAP1. Furthermore, our data suggest that wg has a previously unreported role in specifying the glial‐like cone cells. This activity requires canonical Wg signaling and is linked with Notch pathway activity. Our work broadens the role of canonical Wg signaling to encompass multiple patterning steps in the emerging Drosophila retina. Developmental Dynamics 239:875–884, 2010. © 2010 Wiley‐Liss, Inc.

Related Organizations
Keywords

Cell Death, Receptors, Notch, Gene Expression Regulation, Developmental, Wnt1 Protein, Models, Biological, Frizzled Receptors, Retina, Receptors, G-Protein-Coupled, Drosophila melanogaster, Retinal Cone Photoreceptor Cells, Animals, Drosophila Proteins, Cell Lineage, Neuroglia, Body Patterning, Signal Transduction

  • BIP!
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    citations
    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    13
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Average
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Average
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 10%
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
13
Average
Average
Top 10%
bronze