Árquez Moisés A, Martín-Alonso Samara, Gorelick Robert J, Scott Walter A, Acosta-Hoyos Antonio J, Menéndez-Arias Luis
Grupo de Investigación en Genética, Laboratorio de Genética y Biología Molecular, Facultad de Ciencias Básicas y Biomédicas, Universidad Simón Bolívar, Barranquilla, Colombia.
Ciencias Biomédicas, Universidad del Valle, Cali, Colombia.
Antimicrob Agents Chemother. 2020 Sep 21;64(10). doi: 10.1128/AAC.00958-20.
In HIV-1, development of resistance to AZT (3'-azido-3'-deoxythymidine) is mediated by the acquisition of thymidine analogue resistance mutations (TAMs) (i.e., M41L, D67N, K70R, L210W, T215F/Y, and K219E/Q) in the viral reverse transcriptase (RT). Clinically relevant combinations of TAMs, such as M41L/T215Y or D67N/K70R/T215F/K219Q, enhance the ATP-mediated excision of AZT monophosphate (AZTMP) from the 3' end of the primer, allowing DNA synthesis to continue. Additionally, during HIV-1 maturation, the Gag polyprotein is cleaved to release a mature nucleocapsid protein (NCp7) and two intermediate precursors (NCp9 and NCp15). NC proteins interact with the viral genome and facilitate the reverse transcription process. Using wild-type and TAM-containing RTs, we showed that both NCp9 and NCp15 inhibited ATP-mediated rescue of AZTMP-terminated primers annealed to RNA templates but not DNA templates, while NCp7 had no effect on rescue activity. RNase H inactivation by introducing the active-site mutation E478Q led to the loss of the inhibitory effect shown by NCp9. NCp15 had a stimulatory effect on the RT's RNase H activity not observed with NCp7 and NCp9. However, analysis of RNase H cleavage patterns revealed that in the presence of NCp9, RNA/DNA complexes containing duplexes of 12 bp had reduced stability in comparison with those obtained in the absence of NC or with NCp7 or NCp15. These effects are expected to have a strong influence on the inhibitory action of NCp9 and NCp15 by affecting the efficiency of RNA-dependent DNA polymerization after unblocking DNA primers terminated with AZTMP and other nucleotide analogues.
在HIV-1中,对齐多夫定(3'-叠氮-3'-脱氧胸苷,AZT)产生耐药性是由病毒逆转录酶(RT)中获得胸苷类似物耐药性突变(TAMs)(即M41L、D67N、K70R、L210W、T215F/Y和K219E/Q)介导的。临床上相关的TAMs组合,如M41L/T215Y或D67N/K70R/T215F/K219Q,增强了ATP介导的从引物3'末端切除AZT单磷酸(AZTMP)的能力,使DNA合成得以继续。此外,在HIV-1成熟过程中,Gag多蛋白被切割以释放成熟的核衣壳蛋白(NCp7)和两个中间前体(NCp9和NCp15)。NC蛋白与病毒基因组相互作用并促进逆转录过程。使用野生型和含有TAM的RT,我们发现NCp9和NCp15均抑制ATP介导的与RNA模板退火的AZTMP终止引物的拯救,但对DNA模板无此作用,而NCp7对拯救活性无影响。通过引入活性位点突变E478Q使核糖核酸酶H失活,导致NCp9所显示的抑制作用丧失。NCp15对RT的核糖核酸酶H活性有刺激作用,而NCp7和NCp9未观察到这种作用。然而核糖核酸酶H切割模式分析表明,在存在NCp9的情况下,与不存在NC或存在NCp7或NCp15时相比,含有12 bp双链体的RNA/DNA复合物稳定性降低。预期这些效应会通过影响以AZTMP和其他核苷酸类似物终止的DNA引物解封后RNA依赖性DNA聚合的效率,对NCp9和NCp15的抑制作用产生强烈影响。