Mutation Frequencies in HIV-1 Genome in Regions Containing Efficient RNAi Targets As Calculated from Ultra-Deep Sequencing Data


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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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