Boulme F, Perälä-Heape M, Sarih-Cottin L, Litvak S
Laboratoire Reger, Institut de Biochimie et Génétique Cellulaires du CNRS, IBGC-CNRS, Bordeaux, France.
Biochim Biophys Acta. 1997 Apr 10;1351(3):249-55. doi: 10.1016/s0167-4781(97)00026-2.
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.
对与HIV-1和HIV-2病毒RNA 5'端反式激活应答(TAR)元件的茎环结构重叠的反义寡核苷酸(ODN)进行了测试,以检测它们对HIV-1和HIV-2逆转录酶(RT)合成cDNA的抑制作用。逆转录的抑制具有序列特异性,并且RT相关的核糖核酸酶H活性的存在会增强这种抑制作用。用抗TAR反义寡核苷酸获得的抑制程度明显高于之前使用的其他靶向HIV-1的反义ODN [1]。凝胶阻滞实验显示,16聚体和25聚体的抗TAR HIV-1筛选ODN与靶区域之间形成了稳定的特异性复合物。未观察到非抑制性的22聚体抗TAR ODN和相应对照序列形成复合物。抗TAR ODN靶向HIV-2 RNA 5'区域的第一个茎环,非常强烈地抑制了HIV-2 RT的逆转录。反义寡核苷酸的结构和靶序列会影响退火效率,从而影响逆转录的抑制程度。