4.7 Article

Wallenda regulates JNK-mediated cell death in Drosophila

Journal

CELL DEATH & DISEASE
Volume 6, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/cddis.2015.111

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Funding

  1. National Basic Research Program of China (973 Program) [2011CB943903]
  2. National Natural Science Foundation of China [31071294, 31171413, 31371490]
  3. PhD Programs Foundation of Ministry of Education of China [20120072110023, 20120072120030]
  4. Shanghai Committee of Science and Technology [09DZ2260100, 14JC1406000]

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The c-Jun N-terminal kinase (JNK) pathway plays essential roles in regulating a variety of cellular processes including proliferation, migration and survival. Previous genetic studies in Drosophila have identified numerous cell death regulating genes, providing new insights into the mechanisms for related diseases. Despite the known role of the small GTPase Rac1 in regulating cell death, the downstream components and underlying mechanism remain largely elusive. Here, we show that Rac1 promotes JNK-dependent cell death through Wallenda (Wnd). In addition, we find that Wnd triggers JNK activation and cell death via its kinase domain. Moreover, we show that both MKK4 and Hep are critical for Wnd-induced cell death. Furthermore, Wnd is essential for ectopic Egr-or Rho1-induced JNK activation and cell death. Finally, Wnd is physiologically required for loss of scribble-induced JNK-dependent cell death. Thus, our data suggest that wnd encodes a novel essential cell death regulator in Drosophila.

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