Methylation at lysine 4 of histone H3 in ecdysone-dependent development of Drosophila

Yurii Sedkov, Elizabeth Cho, Svetlana Petruk, Lucy Cherbas, Sheryl T. Smith, Richard S. Jones, Peter Cherbas, Eli Canaani, James B. Jaynes and Alexander Mazo ()
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Yurii Sedkov: Thomas Jefferson University
Elizabeth Cho: Thomas Jefferson University
Svetlana Petruk: Thomas Jefferson University
Lucy Cherbas: Indiana University
Sheryl T. Smith: Thomas Jefferson University
Richard S. Jones: Southern Methodist University
Peter Cherbas: Indiana University
Eli Canaani: Weizmann Institute of Science
James B. Jaynes: Thomas Jefferson University
Alexander Mazo: Thomas Jefferson University

Nature, 2003, vol. 426, issue 6962, 78-83

Abstract: Abstract Steroid hormones fulfil important functions in animal development. In Drosophila, ecdysone triggers moulting and metamorphosis through its effects on gene expression1. Ecdysone works by binding to a nuclear receptor, EcR, which heterodimerizes with the retinoid X receptor homologue Ultraspiracle2,3. Both partners are required for binding to ligand or DNA4,5,6. Like most DNA-binding transcription factors, nuclear receptors activate or repress gene expression by recruiting co-regulators, some of which function as chromatin-modifying complexes7,8. For example, p160 class coactivators associate with histone acetyltransferases and arginine histone methyltransferases9. The Trithorax-related gene of Drosophila encodes the SET domain protein TRR. Here we report that TRR is a histone methyltransferases capable of trimethylating lysine 4 of histone H3 (H3-K4). trr acts upstream of hedgehog (hh) in progression of the morphogenetic furrow, and is required for retinal differentiation. Mutations in trr interact in eye development with EcR, and EcR and TRR can be co-immunoprecipitated on ecdysone treatment. TRR, EcR and trimethylated H3-K4 are detected at the ecdysone-inducible promoters of hh and BR-C in cultured cells, and H3-K4 trimethylation at these promoters is decreased in embryos lacking a functional copy of trr. We propose that TRR functions as a coactivator of EcR by altering the chromatin structure at ecdysone-responsive promoters.

Date: 2003
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DOI: 10.1038/nature02080

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