Literature DB >> 8946916

The Drosophila Jun-N-terminal kinase is required for cell morphogenesis but not for DJun-dependent cell fate specification in the eye.

J R Riesgo-Escovar1, M Jenni, A Fritz, E Hafen.   

Abstract

We cloned and characterized the Drosophila homolog of mammalian Jun-N-terminal kinases (DJNK). We show that DJNK is encoded by basket (bsk). Like hemipterous (hep), which encodes the Drosophila JNK kinase, bsk is required in the embryo for dorsal closure, a process involving coordinate cell shape changes of ectodermal cells. Dorsal closure can also be blocked by dominant negative Drosophila cdc42, which has been shown to act upstream of JNKK in vertebrates. Therefore it appears that the JNK pathway is conserved and that it is involved in controlling cell morphogenesis in Drosophila. Although DJNK efficiently phosphorylates DJun in vitro, bsk function is not required for the specification of cell fate in the developing eye, a process that requires MAP kinase and DJun function.

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Year:  1996        PMID: 8946916     DOI: 10.1101/gad.10.21.2759

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  118 in total

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4.  G protein-coupled receptor signaling through Gq and JNK negatively regulates neural progenitor cell migration.

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5.  Upregulation of forces and morphogenic asymmetries in dorsal closure during Drosophila development.

Authors:  X G Peralta; Y Toyama; M S Hutson; R Montague; S Venakides; D P Kiehart; G S Edwards
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6.  Mitogen-activated protein kinase kinase 7 is an activator of the c-Jun NH2-terminal kinase.

Authors:  C Tournier; A J Whitmarsh; J Cavanagh; T Barrett; R J Davis
Journal:  Proc Natl Acad Sci U S A       Date:  1997-07-08       Impact factor: 11.205

7.  Mixed lineage kinase-dependent JNK activation is governed by interactions of scaffold protein JIP with MAPK module components.

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8.  Diminished MTORC1-Dependent JNK Activation Underlies the Neurodevelopmental Defects Associated with Lysosomal Dysfunction.

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Journal:  Cell Rep       Date:  2015-09-17       Impact factor: 9.423

9.  A genetic screen targeting the tumor necrosis factor/Eiger signaling pathway: identification of Drosophila TAB2 as a functionally conserved component.

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10.  POSH misexpression induces caspase-dependent cell death in Drosophila.

Authors:  Ashley L Lennox; Beth Stronach
Journal:  Dev Dyn       Date:  2010-02       Impact factor: 3.780

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