Med24 and Mdh2 are required for Drosophila larval salivary gland cell death

Authors

  • Lei Wang,

    1. Department of Human Genetics, University of Utah School of Medicine, Salt Lake City, Utah
    Current affiliation:
    1. Laboratory of Genetics, Salk Institute for Biological Studies, 10010 N. Torrey Pines Road, La Jolla, CA 92037
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  • Geanette Lam,

    1. Department of Human Genetics, University of Utah School of Medicine, Salt Lake City, Utah
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  • Carl S. Thummel

    Corresponding author
    1. Department of Human Genetics, University of Utah School of Medicine, Salt Lake City, Utah
    • Department of Human Genetics, University of Utah School of Medicine, 15 N 2030 E Room 2100, Salt Lake City, UT 84112-5330
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Abstract

The steroid hormone ecdysone triggers the rapid destruction of larval tissues through transcriptional cascades that culminate in rpr and hid expression and caspase activation. Here, we show that mutations in Mdh2 and Med24 block caspase cleavage and larval salivary gland cell death. Mdh2 encodes a predicted malate dehydrogenase that localizes to mitochondria. Consistent with this proposed function, Mdh2 mutants have significantly lower levels of ATP and accumulate late-stage citric acid cycle intermediates, suggesting that the cell death defects arise from a deficit in energy production. Med24 encodes a component of the Mediator transcriptional coactivator complex. Unexpectedly, however, expression of the key death regulator genes is normal in Med24 mutant salivary glands. This study identifies novel mechanisms for controlling the destruction of larval tissues during Drosophila metamorphosis and provides new directions for our understanding of steroid-triggered programmed cell death. Developmental Dynamics 239:954–964, 2010. © 2010 Wiley-Liss, Inc.

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