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Specific inhibition of in vitro reverse transcription using antisense oligonucleotides targeted to the TAR regions of HIV-1 and HIV-2

机译:使用靶向HIV-1和HIV-2 TAR区的反义寡核苷酸特异性抑制体外逆转录

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Antisense oligonucleotides (ODNs) overlapping the stem-loop structure of the trans-activating responsive (TAR) element at the 5′ end of HIV-1 and HIV-2 viral RNAs were tested for their inhibitory effect on cDNA synthesis by HIV-1 and HIV-2 reverse transcriptases (RT). Inhibition of reverse transcription is sequence-specific and enhanced by the presence of the RT-associated RNase H activity. The degree of inhibition obtained with the anti-TAR antisense is significantly higher than with other HIV-1 targeted antisense ODNs used before [1]. Gel retardation showed a stable specific complex between the 16- and 25-mer anti-TAR HIV-1 selected ODNs and the target region. No complex was observed with a non-inhibitor 22-mer anti-TAR ODN and with the corresponding control sequences. Targeting of the first stem-loop in the 5′ region of HIV-2 RNA by anti-TAR ODNs inhibited very strongly reverse transcription by HIV-2 RT. The structure of the antisense and the target sequence affect annealing efficiency and hence the degree of inhibition of reverse transcription.
机译:测试了在HIV-1和HIV-2病毒RNA的5'端与反式激活应答(TAR)元件的茎环结构重叠的反义寡核苷酸(ODNs)对HIV-1和HIV-2对cDNA合成的抑制作用HIV-2逆转录酶(RT)。逆转录的抑制是序列特异性的,并通过存在RT相关的RNase H活性而增强。用抗TAR反义获得的抑制程度明显高于以前使用过的其他以HIV-1为目标的反义ODN [1]。凝胶阻滞显示在16聚体和25聚体抗TAR HIV-1选择的ODN与目标区域之间存在稳定的特异性复合物。用非抑制剂的22聚体抗TAR ODN和相应的控制序列未观察到复合物。抗TAR ODNs靶向HIV-2 RNA 5'区域中的第一个茎环可以非常强烈地抑制HIV-2 RT的逆转录。反义的结构和靶序列影响退火效率,并因此影响反转录的抑制程度。

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