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Loss-of-function mutations in either gene suppress the cut wing phenotype resulting from gypsy. During embryonic and pupal development Cut is specifically expressed in the neuroepithelial-derived sensory organ precursor cells SOP cells from which emerge the lineage-related cells of individual ES organs B lochlinger et al. Donady, C. Luong, S. Cremer,

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  • Identification of Genetic Loci That Interact With cut During Drosophila WingMargin Development
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    Seong et al. The bereft gene, a potential target of the neural selector gene cutcontributes to bristle morphogenesis.

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    Although loss-of-function mutations in both genes have been shown to dominantly suppress ct K H oover et al. In addition, females were examined for dominant effects. Thus the BRM complex and other group B candidates may contribute to the regulation of transcription at multiple levels. The JIL-1 tandem kinase mediates histone H3 phosphorylation and is required for maintenance of chromatin structure in Drosophila.

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    This is consistent with previous evidence suggesting that Nipped-B facilitates the activation of cut expression R ollins et al.

    Cell 42 : — Note that the anterior and posterior wing margin is similarly affected. Aigaki, and the Bloomington Stock Center for providing fly stocks.

    Several classes of cut modifiers include loci near known genes that regulate processes influencing cell growth and proliferation, including bratCycEeIF4Aand eIF4E.

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    Identification of Genetic Loci That Interact With cut During Drosophila WingMargin Development

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    It has been proposed that loss of Cut expression in the wing margin results in the failure of the mechanosensory and non-innervated bristles to differentiate, followed by the cell nonautonomous degeneration of the margin.

    The JIL-1 tandem kinase mediates histone H3 phosphorylation and is required for maintenance of chromatin structure in Drosophila. Li, J.

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    Nature : 82— Our genetic analysis indicates that cut -dependent wing-margin patterning also relies upon the activity of Brm, as well as upon the activity of several Brm-associated subunits of both the BAP and the PBAP complex. The genetic interaction data with ct 53d are summarized in Table 2.

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    Brantley, G.

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    USA : — C lola mRNA is expressed ubiquitously in wild-type wing imaginal tissue. Of the genes that were identified through these screens, the BTB-domain zinc-finger gene longitudinals lacking lola and several genes encoding subunits of the Brahma chromatin-remodeling complexes were investigated further with regard to their interaction with cut during wing-margin development.

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    The GS vector contains bidirectional upstream activating sequences UASwhich bind the transcriptional activator Gal4. CCAAT displacement protein as a repressor of the myelomonocytic-specific gpphox gene promoter.

    GS lines were retested by crossing to both ct K ; CGal4 and ct K alone to determine if suppression resulted from overexpression or from gene disruption.

    The ability of individual GS lines to suppress ct K was scored as described above.

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    1. Aigaki, and the Bloomington Stock Center for providing fly stocks. The regulation of the distal cut wing enhancer requires the activity of both enhancer-binding and enhancer-facilitator proteins.

    2. A hidden program in Drosophila peripheral neurogenesis revealed: fundamental principles underlying sensory organ diversity. The ct 53d allele disrupts Cut expression primarily in the presumptive wing tip, which corresponds to a severe loss of wing tissue in the distal-most region of the adult wing.

    3. The Drosophila rhomboid gene mediates the localized formation of wing veins and interacts genetically with components of the EGF-R signaling pathway.