Abstract |
The role of the 3'untranslated region (UTR) of the dengue virus (DENV) genome during viral translation remains to be elucidated. We assessed the contribution of well-defined RNA elements in the 3'UTR of DENV-2 to viral translation using a virus-induced reporting gene system and deoxyribozymes (DRzs) targeting the 3'UTR of the DENV-2 genome. Results show that mRNAs carrying a deletion of repeated conserved sequence (RCS2)-CS2 are translated less efficiently than wild type mRNAs. However, mRNAs with a deletion of CS1-stem loop (SL) are translated more efficiently. Thus, CS1-SL and RCS2-CS2 may have different effects on translational regulation. Additionally, the translation-suppressing effect of CS1-SL or the SL element is further confirmed in DENV-2-infected cells using DRzs. Mutagenesis studies show that, rather than the secondary structure, nucleotides 10663-10677 and 10709-10723 are responsible for translational suppression of SL. Overall, our results demonstrate that sequences and elements within the DENV-2 3'UTR regulate viral translation.
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Authors | Yan Wei, Chengfeng Qin, Tao Jiang, Xiaofeng Li, Hui Zhao, Zhongyu Liu, Yongqiang Deng, Ran Liu, Shuiping Chen, Man Yu, Ede Qin |
Journal | The American journal of tropical medicine and hygiene
(Am J Trop Med Hyg)
Vol. 81
Issue 5
Pg. 817-24
(Nov 2009)
ISSN: 1476-1645 [Electronic] United States |
PMID | 19861617
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- 3' Untranslated Regions
- RNA, Messenger
- RNA, Viral
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Topics |
- 3' Untranslated Regions
(physiology)
- Animals
- Cell Line
- Cricetinae
- Dengue Virus
(classification, genetics)
- Gene Expression Regulation, Viral
(physiology)
- Genome, Viral
- Protein Biosynthesis
- RNA, Messenger
(genetics, metabolism)
- RNA, Viral
(genetics, metabolism)
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