Previous Article | Next Article 
Molecular and Cellular Biology, July 2005, p. 5590-5598, Vol. 25, No. 13
0270-7306/05/$08.00+0 doi:10.1128/MCB.25.13.5590-5598.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
DREF Is Required for Efficient Growth and Cell Cycle Progression in Drosophila Imaginal Discs
Joogyung Hyun,
Heinrich Jasper, and
Dirk Bohmann*
Department of Biomedical Genetics, The Aab Institute of Biomedical Sciences, University of Rochester Medical Center, 601 Elmwood Avenue, Box 633, Rochester, NY 14642
Received 15 December 2004/
Returned for modification 26 January 2005/
Accepted 4 April 2005
Based on overexpression studies and target gene analyses, the transcription factor DNA replication-related element factor (DREF) has been proposed to regulate growth and replication in Drosophila melanogaster. Here we present loss-of-function experiments to analyze the contribution of DREF to these processes. RNA interference-mediated extinction of DREF function in vivo demonstrates a requirement for the protein for normal progression through the cell cycle and consequently for growth of imaginal discs and the derived adult organs. We show that DREF regulates the expression of genes that are required for the transition of imaginal disc cells through S phase. In conditions of suppressed apoptosis, DREF activation can cause overgrowth of developing organs. These data establish DREF as a global regulator of transcriptional programs that mediate cell proliferation and organ growth during animal development.
* Corresponding author. Mailing address: Department of Biomedical Genetics, University of Rochester Medical Center, 601 Elmwood Avenue, Box 633, Rochester, NY 14642. Phone: (585) 273-1446. Fax: (585) 273-1450. E-mail: dirk_bohmann{at}urmc.rochester.edu.
Molecular and Cellular Biology, July 2005, p. 5590-5598, Vol. 25, No. 13
0022-538X/05/$08.00+0 doi:10.1128/MCB.25.13.5590-5598.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Nakamura, K., Ida, H., Yamaguchi, M.
(2008). Transcriptional regulation of the Drosophila moira and osa genes by the DREF pathway. Nucleic Acids Res
36: 3905-3915
[Abstract]
[Full Text]
-
Isogai, Y., Keles, S., Prestel, M., Hochheimer, A., Tjian, R.
(2007). Transcription of histone gene cluster by differential core-promoter factors. Genes Dev.
21: 2936-2949
[Abstract]
[Full Text]
-
Kugler, S. J., Nagel, A. C.
(2007). putzig Is Required for Cell Proliferation and Regulates Notch Activity in Drosophila. Mol. Biol. Cell
18: 3733-3740
[Abstract]
[Full Text]
-
Kim, Y. S., Shin, M. J., Yang, D. J., Yamaguchi, M., Park, S. Y., Yoo, M. A.
(2007). Transcriptional regulation of the Drosophila ANT gene by the DRE/DREF system. GENES CELLS
12: 569-579
[Abstract]
[Full Text]
-
Yamashita, D., Sano, Y., Adachi, Y., Okamoto, Y., Osada, H., Takahashi, T., Yamaguchi, T., Osumi, T., Hirose, F.
(2007). hDREF Regulates Cell Proliferation and Expression of Ribosomal Protein Genes. Mol. Cell. Biol.
27: 2003-2013
[Abstract]
[Full Text]
-
Yamashita, D., Komori, H., Higuchi, Y., Yamaguchi, T., Osumi, T., Hirose, F.
(2007). Human DNA Replication-related Element Binding Factor (hDREF) Self-association via hATC Domain Is Necessary for Its Nuclear Accumulation and DNA Binding. J. Biol. Chem.
282: 7563-7575
[Abstract]
[Full Text]
Copyright © 2005 by the American Society for Microbiology. All rights reserved.