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1.
PLoS One ; 9(8): e106211, 2014.
Article in English | MEDLINE | ID: mdl-25157415

ABSTRACT

During development, tissues and organs must coordinate growth and patterning so they reach the right size and shape. During larval stages, a dramatic increase in size and cell number of Drosophila wing imaginal discs is controlled by the action of several signaling pathways. Complex cross-talk between these pathways also pattern these discs to specify different regions with different fates and growth potentials. We show that the Notch signaling pathway is both required and sufficient to inhibit the activity of Yorkie (Yki), the Salvador/Warts/Hippo (SWH) pathway terminal transcription activator, but only in the central regions of the wing disc, where the TEAD factor and Yki partner Scalloped (Sd) is expressed. We show that this cross-talk between the Notch and SWH pathways is mediated, at least in part, by the Notch target and Sd partner Vestigial (Vg). We propose that, by altering the ratios between Yki, Sd and Vg, Notch pathway activation restricts the effects of Yki mediated transcription, therefore contributing to define a zone of low proliferation in the central wing discs.


Subject(s)
Drosophila Proteins/metabolism , Drosophila Proteins/physiology , Drosophila melanogaster/metabolism , Imaginal Discs/metabolism , Nuclear Proteins/metabolism , Receptors, Notch/physiology , Trans-Activators/metabolism , Animals , Cell Proliferation , Drosophila Proteins/genetics , Gene Expression Regulation, Developmental , Imaginal Discs/cytology , Nuclear Proteins/genetics , Signal Transduction , Trans-Activators/genetics , Transcription Factors/genetics , Transcription Factors/metabolism , Transcription, Genetic , YAP-Signaling Proteins
2.
PLoS One ; 8(9): e75632, 2013.
Article in English | MEDLINE | ID: mdl-24086596

ABSTRACT

Notch signaling regulates many fundamental events including lateral inhibition and boundary formation to generate very reproducible patterns in developing tissues. Its targets include genes of the bHLH hairy and Enhancer of split [E(spl)] family, which contribute to many of these developmental decisions. One member of this family in Drosophila, deadpan (dpn), was originally found to have functions independent of Notch in promoting neural development. Employing genome-wide chromatin-immunoprecipitation we have identified several Notch responsive enhancers in dpn, demonstrating its direct regulation by Notch in a range of contexts including the Drosophila wing and eye. dpn expression largely overlaps that of several E(spl) genes and the combined knock-down leads to more severe phenotypes than either alone. In addition, Dpn contributes to the establishment of Cut expression at the wing dorsal-ventral (D/V) boundary; in its absence Cut expression is delayed. Furthermore, over-expression of Dpn inhibits expression from E(spl) gene enhancers, but not vice versa, suggesting that dpn contributes to a feed-back mechanism that limits E(spl) gene expression following Notch activation. Thus the combined actions of dpn and E(spl) appear to provide a mechanism that confers an initial rapid output from Notch activity which becomes self-limited via feedback between the targets.


Subject(s)
Basic Helix-Loop-Helix Transcription Factors/genetics , Basic Helix-Loop-Helix Transcription Factors/metabolism , Drosophila Proteins/genetics , Drosophila Proteins/metabolism , Drosophila/growth & development , Nuclear Proteins/genetics , Nuclear Proteins/metabolism , Receptors, Notch/genetics , Receptors, Notch/metabolism , Animals , DNA-Binding Proteins , Drosophila/genetics , Drosophila/metabolism , Eye/growth & development , Eye/metabolism , Gene Expression Regulation, Developmental/genetics , Homeodomain Proteins/genetics , Homeodomain Proteins/metabolism , Repressor Proteins/genetics , Repressor Proteins/metabolism , Transcription Factors/genetics , Transcription Factors/metabolism , Wings, Animal/growth & development , Wings, Animal/metabolism
3.
Development ; 136(24): 4089-98, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19906847

ABSTRACT

Asymmetric cell divisions generate sibling cells of distinct fates ('A', 'B') and constitute a fundamental mechanism that creates cell-type diversity in multicellular organisms. Antagonistic interactions between the Notch pathway and the intrinsic cell-fate determinant Numb appear to regulate asymmetric divisions in flies and vertebrates. During these divisions, productive Notch signaling requires sanpodo, which encodes a novel transmembrane protein. Here, we demonstrate that Drosophila sanpodo plays a dual role to regulate Notch signaling during asymmetric divisions - amplifying Notch signaling in the absence of Numb in the 'A' daughter cell and inhibiting Notch signaling in the presence of Numb in the 'B' daughter cell. In so doing, sanpodo ensures the asymmetry in Notch signaling levels necessary for the acquisition of distinct fates by the two daughter cells. These findings answer long-standing questions about the restricted ability of Numb and Sanpodo to inhibit and to promote, respectively, Notch signaling during asymmetric divisions.


Subject(s)
Cell Lineage/physiology , Drosophila Proteins/physiology , Drosophila , Receptors, Notch/physiology , Animals , Cell Differentiation/physiology , Cell Division/physiology , Drosophila/embryology , Drosophila/metabolism , Embryo, Nonmammalian/embryology , Embryo, Nonmammalian/metabolism , Gene Expression Regulation, Developmental , Juvenile Hormones/physiology , Microfilament Proteins/physiology , Signal Transduction
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