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Specific implications of the HIV-1 nucleocapsid zinc fingers in the annealing of the primer binding site complementary sequences during the obligatory plus strand transfer

机译:HIV-1核衣壳锌指在强制性和链转移过程中引物结合位点互补序列退火中的特殊含义

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摘要

Synthesis of the HIV-1 viral DNA by reverse transcriptase involves two obligatory strand transfer reactions. The second strand transfer corresponds to the annealing of the (−) and (+) DNA copies of the primer binding site (PBS) sequence which is chaperoned by the nucleocapsid protein (NCp7). NCp7 modifies the (+)/(−)PBS annealing mechanism by activating a loop–loop kissing pathway that is negligible without NCp7. To characterize in depth the dynamics of the loop in the NCp7/PBS nucleoprotein complexes, we investigated the time-resolved fluorescence parameters of a (−)PBS derivative containing the fluorescent nucleoside analogue 2-aminopurine at positions 6, 8 or 10. The NCp7-directed switch of (+)/(−)PBS annealing towards the loop pathway was associated to a drastic restriction of the local DNA dynamics, indicating that NCp7 can ‘freeze’ PBS conformations competent for annealing via the loops. Moreover, the modifications of the PBS loop structure and dynamics that govern the annealing reaction were found strictly dependent on the integrity of the zinc finger hydrophobic platform. Our data suggest that the two NCp7 zinc fingers are required to ensure the specificity and fidelity of the second strand transfer, further underlining the pivotal role played by NCp7 to control the faithful synthesis of viral HIV-1 DNA.
机译:通过逆转录酶合成HIV-1病毒DNA涉及两个强制性链转移反应。第二次链转移对应于被核衣壳蛋白(NCp7)陪伴的引物结合位点(PBS)序列的(-)和(+)DNA拷贝的退火。 NCp7通过激活不使用NCp7可以忽略的环-环接吻途径来修饰(+)/(-)PBS退火机制。为了深入表征NCp7 / PBS核蛋白复合物中环的动力学,我们研究了在位置6、8或10处含有荧光核苷类似物2-氨基嘌呤的(-)PBS衍生物的时间分辨荧光参数。 (+)/(-)PBS定向向环状途径的定向转换与局部DNA动力学的严格限制有关,这表明NCp7可以“冻结”通过环状进行退火的PBS构象。此外,发现严格取决于锌指疏水性平台的完整性的PBS环结构的修饰和控制退火反应的动力学。我们的数据表明,需要两个NCp7锌指来确保第二条链转移的特异性和保真度,从而进一步强调了NCp7在控制病毒HIV-1 DNA忠实合成中所起的关键作用。

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