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Chromosome Structure and Human Immunodeficiency Virus Type 1 cDNA Integration: Centromeric Alphoid Repeats Are a Disfavored Target

机译:染色体结构和人类免疫缺陷病毒1型cDNA整合:着丝粒的拟南芥重复是不利的目标。

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摘要

Integration of retroviral cDNA into host chromosomal DNA is an essential and distinctive step in viral replication. Despite considerable study, the host determinants of sites for integration have not been fully clarified. To investigate integration site selection in vivo, we used two approaches. (i) We have analyzed the host sequences flanking 61 human immunodeficiency virus type 1 (HIV-1) integration sites made by experimental infection and compared them to a library of 104 control sequences. (ii) We have also analyzed HIV-1 integration frequencies near several human repeated-sequence DNA families, using a repeat-specific PCR-based assay. At odds with previous reports from smaller-scale studies, we found no strong biases either for or against integration near repetitive sequences such as Alu or LINE-1 elements. We also did not find a clear bias for integration in transcription units as proposed previously, although transcription units were found somewhat more frequently near integration sites than near controls. However, we did find that centromeric alphoid repeats were selectively absent at integration sites. The repeat-specific PCR-based assay also indicated that alphoid repeats were disfavored for integration in vivo but not as naked DNA in vitro. Evidently the distinctive DNA organization at centromeres disfavors cDNA integration. We also found a weak consensus sequence for host DNA at integration sites, and assays of integration in vitro indicated that this sequence is favored as naked DNA, revealing in addition an influence of target primary sequence.
机译:逆转录病毒cDNA整合入宿主染色体DNA是病毒复制中必不可少的独特步骤。尽管进行了大量研究,但整合站点的宿主决定因素尚未完全阐明。为了研究体内整合位点的选择,我们使用了两种方法。 (i)我们分析了由实验感染产生的61个1型人类免疫缺陷病毒(HIV-1)整合位点两侧的宿主序列,并将其与104个控制序列的文库进行了比较。 (ii)我们还使用基于重复特异性PCR的分析方法分析了几个人类重复序列DNA家族附近的HIV-1整合频率。与小规模研究的先前报道不同,我们没有发现对重复序列(如Alu或LINE-1元件)附近的整合有强烈的偏见。我们也没有发现以前提出的在转录单位中整合的明显偏向,尽管在整合位点附近发现转录单位的频率比在对照附近更高。但是,我们确实发现在整合位点有选择地不存在着着丝粒的拟南芥重复序列。基于重复序列特异性PCR的测定还表明,在体内整合时不利于脂质体重复,但在体外则不作为裸露的DNA。很明显,着丝粒的独特DNA组织不利于cDNA整合。我们还在整合位点发现了宿主DNA的弱共有序列,体外整合试验表明该序列更适合作为裸露的DNA,另外还揭示了靶标一级序列的影响。

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