Downregulation of human adenovirus DNA polymerase gene by modified siRNAs
- 作者: Nikitenko N.A.1, Speiseder T.2, Chernolovskaya E.L.3, Zenkova M.A.3, Dobner T.2, Prassolov V.S.1
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隶属关系:
- Engelhardt Institute of Molecular Biology
- Heinrich Pette Institute–Leibniz Institute for Experimental Virology
- Institute of Chemical Biology and Fundamental Medicine Siberian Branch
- 期: 卷 50, 编号 1 (2016)
- 页面: 164-167
- 栏目: Short Communications
- URL: https://journals.rcsi.science/0026-8933/article/view/162551
- DOI: https://doi.org/10.1134/S0026893316010155
- ID: 162551
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详细
Human adenoviruses, in particular D8, D19, and D37, cause ocular infections. Currently, there is no available causally directed treatment, which efficiently counteracts adenoviral infectious diseases. In our previous work, we showed that gene silencing by means of RNA interference is an effective approach for downregulation of human species D adenoviruses replication. In this study, we compared the biological activity of siRNAs and their modified analogs targeting human species D adenoviruses DNA polymerase. We found that one of selectively 2’-O-methyl modified siRNAs mediates stable and long-lasting suppression of the target gene (12 days post transfection). We suppose that this siRNA can be used as a potential therapeutic agent against human species D adenoviruses.
作者简介
N. Nikitenko
Engelhardt Institute of Molecular Biology
Email: prassolov45@mail.ru
俄罗斯联邦, Moscow, 119991
T. Speiseder
Heinrich Pette Institute–Leibniz Institute for Experimental Virology
Email: prassolov45@mail.ru
德国, Hamburg, D-20251
E. Chernolovskaya
Institute of Chemical Biology and Fundamental Medicine Siberian Branch
Email: prassolov45@mail.ru
俄罗斯联邦, Novosibirsk, 630090
M. Zenkova
Institute of Chemical Biology and Fundamental Medicine Siberian Branch
Email: prassolov45@mail.ru
俄罗斯联邦, Novosibirsk, 630090
T. Dobner
Heinrich Pette Institute–Leibniz Institute for Experimental Virology
Email: prassolov45@mail.ru
德国, Hamburg, D-20251
V. Prassolov
Engelhardt Institute of Molecular Biology
编辑信件的主要联系方式.
Email: prassolov45@mail.ru
俄罗斯联邦, Moscow, 119991
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