Mutation Frequencies in HIV-1 Genome in Regions Containing Efficient RNAi Targets As Calculated from Ultra-Deep Sequencing Data
- 作者: Kretova O.V.1, Gorbacheva M.A.1, Fedoseeva D.M.1, Kravatsky Y.V.1, Chechetkin V.R.1, Tchurikov N.A.1
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隶属关系:
- Engelhardt Institute of Molecular Biology
- 期: 卷 52, 编号 3 (2018)
- 页面: 393-397
- 栏目: Genomics. Trascriptomics
- URL: https://journals.rcsi.science/0026-8933/article/view/163533
- DOI: https://doi.org/10.1134/S002689331803007X
- ID: 163533
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详细
HIV-1 is one of the most variable viruses. The development of gene therapy technology using RNAi for AIDS/HIV-1 treatment is a potential alternative for traditional anti-retroviral therapy. Anti-HIV-1 siRNA should aim to exploit the most conserved viral targets. Using the deep sequencing of potential RNAi targets in 100-nt HIV-1 genome fragments from the clinical HIV-1 subtype A isolates in Russia, we found that the frequencies of all possible transversions and transitions in certain RNAi targets are 3–38 times lower than in adjacent sequences. Therefore, these targets are conserved. We propose the development of these RNAi targets for AIDS/HIV-1 treatment. Deep sequencing also enables the detection of the characteristic mutational bias of RT during the replication of viral RNA.
作者简介
O. Kretova
Engelhardt Institute of Molecular Biology
Email: tchurikov@eimb.ru
俄罗斯联邦, Moscow, 119334
M. Gorbacheva
Engelhardt Institute of Molecular Biology
Email: tchurikov@eimb.ru
俄罗斯联邦, Moscow, 119334
D. Fedoseeva
Engelhardt Institute of Molecular Biology
Email: tchurikov@eimb.ru
俄罗斯联邦, Moscow, 119334
Y. Kravatsky
Engelhardt Institute of Molecular Biology
Email: tchurikov@eimb.ru
俄罗斯联邦, Moscow, 119334
V. Chechetkin
Engelhardt Institute of Molecular Biology
Email: tchurikov@eimb.ru
俄罗斯联邦, Moscow, 119334
N. Tchurikov
Engelhardt Institute of Molecular Biology
编辑信件的主要联系方式.
Email: tchurikov@eimb.ru
俄罗斯联邦, Moscow, 119334
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