Lavignon M, Bertrand J R, Rayner B, Imbach J L, Malvy C, Paoletti C
UA 147 CNRS, U 140 INSERM, Institut Gustave Roussy, Villejuif, France.
Biochem Biophys Res Commun. 1989 Jun 30;161(3):1184-90. doi: 10.1016/0006-291x(89)91367-3.
After parallel hybridization to complementary template RNA, alpha-anomeric oligonucleotides are not primers for Moloney murine leukemia virus reverse transcriptase. As can be expected they are competitors of classical primer oligonucleotides (beta-anomeric). They therefore inhibit the RNA dependent DNA polymerase activity of Moloney murine leukemia virus reverse transcriptase with either homopolymeric or heteropolymeric substrates. Non complementary alpha-oligonucleotides display no inhibitory activity. alpha-Oligonucleotides are therefore potential candidates for inhibition of retroviral reverse transcriptases by interference with the primer binding sites.
与互补模板RNA进行平行杂交后,α-异头寡核苷酸不是莫洛尼鼠白血病病毒逆转录酶的引物。可以预料,它们是经典引物寡核苷酸(β-异头)的竞争者。因此,它们在同聚物或杂聚物底物存在时,均能抑制莫洛尼鼠白血病病毒逆转录酶的RNA依赖性DNA聚合酶活性。非互补的α-寡核苷酸不显示抑制活性。因此,α-寡核苷酸有可能通过干扰引物结合位点来抑制逆转录病毒逆转录酶。