Journal article
UTX coordinates steroid hormone-mediated autophagy and cell death
D Denton, MT Aung-Htut, N Lorensuhewa, S Nicolson, W Zhu, K Mills, D Cakouros, A Bergmann, S Kumar
Nature Communications | NATURE PUBLISHING GROUP | Published : 2013
DOI: 10.1038/ncomms3916
Abstract
Correct spatial and temporal induction of numerous cell type-specific genes during development requires regulated removal of the repressive histone H3 lysine 27 trimethylation (H3K27me3) modification. Here we show that the H3K27me3 demethylase dUTX is required for hormone-mediated transcriptional regulation of apoptosis and autophagy genes during ecdysone-regulated programmed cell death of Drosophila salivary glands. We demonstrate that dUTX binds to the nuclear hormone receptor complex Ecdysone Receptor/Ultraspiracle, and is recruited to the promoters of key apoptosis and autophagy genes. Salivary gland cell death is delayed in dUTX mutants, with reduced caspase activity and autophagy that ..
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Awarded by National Institutes of Health
Funding Acknowledgements
This work was supported by the National Health and Medical Research Council (NHMRC) Project Grants 626903 and 626923, and a Senior Principal Research Fellowship 1002863 to S. K., as well as R01 GM068016 from the National Institutes of Health (NIH) to A. B. We thank the Australian Drosophila Research Support Facility, Vienna Drosophila RNAi Center and Bloomington Drosophila Stock Center for Drosophila stocks, Developmental Studies Hybridoma Bank (University of Iowa) for antibodies,