FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Kallio, J., Myllymäki, H., Grönholm, J., Armstrong, M., Vanha-aho, L.M., Mäkinen, L., Silvennoinen, O., Valanne, S., Rämet, M. (2010). Eye transformer is a negative regulator of Drosophila JAK/STAT signaling.  FASEB J. 24(11): 4467--4479.
FlyBase ID
FBrf0212202
Publication Type
Research paper
Abstract
JAK/STAT signaling pathway is evolutionarily conserved and tightly regulated. We carried out a reporter-based genome-wide RNAi in vitro screen to identify genes that regulate Drosophila JAK/STAT pathway and found 5 novel regulators. Of these, CG14225 is a negative regulator structurally related to the Drosophila JAK/STAT pathway receptor Domeless, especially in the extracellular domain, and to the mammalian IL-6 receptor and the signal transducer gp130. CG14225 coimmunoprecipitates with Domeless and its associated kinase hopscotch in S2 cells. CG14225 RNAi caused hyperphosphorylation of the transcription factor Stat92E in S2 cells on stimulation with the Drosophila JAK/STAT pathway ligand unpaired. CG14225 RNAi in vivo hyperactivated JAK/STAT target genes on septic injury and enhanced unpaired-induced eye overgrowth, and was thus named the eye transformer (ET). In the gastrointestinal infection model, where JAK/STAT signaling is important for stem cell renewal, CG14225/ET RNAi was protective in vivo. In conclusion, we have identified ET as a novel negative regulator of the Drosophila JAK/STAT pathway both in vitro and in vivo, and it functions in regulating Stat92E phosphorylation.
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PubMed Central ID
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    FASEB J.
    Title
    FASEB Journal (Federation of American Societies for Experimental Biology)
    Publication Year
    1987-
    ISBN/ISSN
    0892-6638
    Data From Reference
    Alleles (7)
    Gene Groups (3)
    Genes (15)
    Physical Interactions (3)
    Cell Lines (1)
    Insertions (1)
    Transgenic Constructs (6)