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GENES & DEVELOPMENT 19:2540-2545, 2005
©2005 by Cold Spring Harbor Laboratory Press; ISSN 0890-9369/ $5.00
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RESEARCH COMMUNICATION

The Drosophila nucleosome remodeling factor NURF is required for Ecdysteroid signaling and metamorphosis

Paul Badenhorst1,2,6, Hua Xiao1, Lucy Cherbas3, So Yeon Kwon2, Matt Voas4, Ilaria Rebay4, Peter Cherbas3 and Carl Wu1,5

1 Laboratory of Molecular Cell Biology, National Cancer Institute, NIH, Bethesda, Maryland 20814, USA; 2 Department of Anatomy, Institute of Biomedical Research, University of Birmingham, Edgbaston B15 2TT, United Kingdom; 3 Department of Biology and Center for Genomics and Bioinformatics, Indiana University, Bloomington, Indiana 47405, USA; 4 Whitehead Institute, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA

Drosophila NURF is an ISWI-containing ATP-dependent chromatin remodeling complex that regulates transcription by catalyzing nucleosome sliding. To determine in vivo gene targets of NURF, we performed whole genome expression analysis on mutants lacking the NURF-specific subunit NURF301. Strikingly, a large set of ecdysone-responsive targets is included among several hundred NURF-regulated genes. Null Nurf301 mutants do not undergo larval to pupal metamorphosis, and also enhance dominant-negative mutations in ecdysone receptor. Moreover, purified NURF binds EcR in an ecdysone-dependent manner, suggesting it is a direct effector of nuclear receptor activity. The conservation of NURF in mammals has broad implications for steroid signaling.

[Keywords: NURF; chromatin remodeling; chromatin; Drosophila; Ecdysteroid; ISWI]

Received June 9, 2005; revised version accepted August 26, 2005.


Supplemental material is available at http://www.genesdev.org.

Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.1342605.

Corresponding authors.

6 E-MAIL p.w.badenhorst{at}bham.ac.uk; FAX 44-121-414-3599.

5 E-MAIL carlwu{at}helix.nih.gov; FAX (301) 435-3697.


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