Abstract |
A computer-assisted analysis identified tentative target sequences for regulatory proteins including ecdysone-inducible factors such as BmFTZ-F1 and Broad-Complex Z4 (BR-C Z4) in the ie1 promoter of BmNPV. A transient expression experiment using BmN cells and a series of truncated ie1 promoter constructs demonstrated that the activity of the ie1 promoter responded to alpha- ecdysone and 20-hydroxyecdysone, which required a tridecameric nucleotide stretch (ie1EcRE, 5'-GTGTTATCGACCT-3') homologous to the ecdysone response element reported for Drosophila (DmEcRE). RT-PCR demonstrated the expression of BmEcR and BmUSP, which are required as ecdysone-specific activators for EcRE-mediated activation, in BmN cells. Furthermore, the ie1 EcRE-mediated response was confirmed by using a recombinant BmNPV possessing a luciferase gene under the control of the ie1 promoter with or without ie1 EcRE. This is the first report of an ecdysone response element in a baculoviral gene promoter. These results also suggested that the regulation of the ie1 by ecdysone may militate viral replication at least under certain conditions during natural infections in vivo.
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Authors | K Kojima, K Oritani, T Nakatsukasa, S Asano, K Sahara, H Bando |
Journal | Virus research
(Virus Res)
Vol. 130
Issue 1-2
Pg. 202-9
(Dec 2007)
ISSN: 0168-1702 [Print] Netherlands |
PMID | 17658648
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Ecdysone
- Ecdysterone
- Luciferases
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Topics |
- Animals
- Artificial Gene Fusion
- Baculoviridae
(genetics, physiology)
- Bombyx
- Cell Line
- Ecdysone
(metabolism)
- Ecdysterone
(metabolism)
- Gene Expression Regulation
- Genes, Immediate-Early
- Genes, Reporter
- Luciferases
(biosynthesis, genetics)
- Promoter Regions, Genetic
- Response Elements
(genetics)
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