首页> 外文期刊>American journal of infectious diseases. >HIGH FREQUENCY OF STOP CODONS IN THE HUMAN IMMUNODEFICIENCY VIRUS?1 PROTEASE GENE FRAME IN HUMAN IMMUNODEFICIENCY VIRUS+ INDIVIDUALS WITH BELOW DETECTABLE LEVELS OF PLASMA VIREMIA DURING HIGHLY ACTIVE ANTIRETROVIRAL THERAPY
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HIGH FREQUENCY OF STOP CODONS IN THE HUMAN IMMUNODEFICIENCY VIRUS?1 PROTEASE GENE FRAME IN HUMAN IMMUNODEFICIENCY VIRUS+ INDIVIDUALS WITH BELOW DETECTABLE LEVELS OF PLASMA VIREMIA DURING HIGHLY ACTIVE ANTIRETROVIRAL THERAPY

机译:在高活性抗病毒治疗期间,人免疫缺陷病毒+个体中人免疫缺陷病毒+个体的蛋白酶基因终止框频率很高。

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We performed sequence analysis of HIV?1 proviral protease gene fragment (560 base pairs) amplified from ex?vivo peripheral blood mononuclear cells of 83 HIV+ individuals with Below Detectable Levels (BDL) (<20?40 RNA copies/ml plasma) and detectable levels of plasma HIV viremia while on HAART. Noteworthy was the systematic presence of stop codons identified only in the BDL group and not in individuals with detectable plasma viremia (p<0.0001). The stop codons dominated positions 16 and 157 in the protease gene. This suggests that specific mutations in the protease gene possibly provide transitory molecular control of viral replication to below detectable levels in plasma during HAART. Thus, these mutations could potentially be exploited for long?term control of HIV.
机译:我们对83个HIV +个体的离体外周血单个核细胞中扩增的HIV?1前病毒蛋白酶基因片段(560个碱基对)进行了序列分析,其检测水平低于(BDL)(<20?40 RNA拷贝/ ml血浆)并且可检测进行HAART时血浆HIV病毒血症的水平。值得注意的是,仅在BDL组中发现了终止密码子的系统存在,而在血浆病毒血症可检测到的个体中则没有发现(p <0.0001)。终止密码子在蛋白酶基因中位于位置16和157。这表明在HAART期间,蛋白酶基因中的特定突变可能提供对病毒复制的瞬时分子控制,使其低于血浆中可检测的水平。因此,这些突变可能被潜在地用于HIV的长期控制。

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