Permanent URL to this publication: http://dx.doi.org/10.5167/uzh-742
Hulf, T; Bellosta, P; Furrer, M; Steiger, D; Svensson, D; Barbour, A D; Gallant, P (2005). Whole-genome analysis reveals a strong positional bias of conserved dMyc-dependent E-boxes. Molecular and Cellular Biology, 25(9):3401-3410.
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Abstract
Myc is a transcription factor with diverse biological effects ranging from the control of cellular proliferation and growth to the induction of apoptosis. Here we present a comprehensive analysis of the transcriptional targets of the sole Myc ortholog in Drosophila melanogaster, dMyc. We show that the genes that are down-regulated in response to dmyc inhibition are largely identical to those that are up-regulated after dMyc overexpression and that many of them play a role in growth control. The promoter regions of these targets are characterized by the presence of the E-box sequence CACGTG, a known dMyc binding site. Surprisingly, a large subgroup of (functionally related) dMyc targets contains a single E-box located within the first 100 nucleotides after the transcription start site. The relevance of this E-box and its position was confirmed by a mutational analysis of a selected dMyc target and by the observation of its evolutionary conservation in a different Drosophila species, Drosophila pseudoobscura. These observations raise the possibility that a subset of Myc targets share a distinct regulatory mechanism.
| Item Type: | Journal Article, refereed, original work |
|---|---|
| Communities & Collections: | 07 Faculty of Science > Institute of Zoology (former) |
| DDC: | 570 Life sciences; biology 590 Animals (Zoology) |
| Language: | English |
| Date: | 01 May 2005 |
| Deposited On: | 11 Feb 2008 13:17 |
| Last Modified: | 23 Nov 2012 14:27 |
| Publisher: | American Society for Microbiology (ASM) |
| ISSN: | 0270-7306 |
| Publisher DOI: | 10.1128/MCB.25.9.3401-3410.2005 |
| PubMed ID: | 15831447 |
| WoS Citation Count: | 35 |
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