Kumar Pavan P, Mehta Sameet, Purbey Prabhat Kumar, Notani Dimple, Jayani Ranveer S, Purohit Hemant J, Raje Dhananjay V, Ravi Dyavar S, Bhonde Ramesh R, Mitra Debashis, Galande Sanjeev
National Centre for Cell Science, NCCS Complex, Ganeshkhind, Pune 411007, India.
J Virol. 2007 Jun;81(11):5617-27. doi: 10.1128/JVI.01405-06. Epub 2007 Mar 21.
Retroviral integration has recently been shown to be nonrandom, favoring transcriptionally active regions of chromatin. However, the mechanism for integration site selection by retroviruses is not clear. We show here the occurrence of Alu-like motifs in the sequences flanking the reported viral integration sites that are significantly different from those obtained from the randomly picked sequences from the human genome, suggesting that unique primary sequence features exist in the genomic regions targeted by human immunodeficiency virus type 1 (HIV-1). Additionally, these sequences were preferentially bound by SATB1, the T lineage-restricted chromatin organizer, in vitro and in vivo. Alu repeats make up nearly 10% of the human genome and have been implicated in the regulation of transcription. To specifically isolate sequences flanking the viral integration sites and also harboring both Alu-like repeats and SATB1-binding sites, we combined chromatin immunoprecipitation with sequential PCRs. The cloned sequences flanking HIV-1 integration sites were specifically immunoprecipitated and amplified from the pool of anti-SATB1-immunoprecipitated genomic DNA fragments isolated from HIV-1 NL4.3-infected Jurkat T-cell chromatin. Moreover, many of these sequences were preferentially partitioned in the DNA associated tightly with the nuclear matrix and not in the chromatin loops. Strikingly, many of these regions were disfavored for integration when SATB1 was silenced, providing unequivocal evidence for its role in HIV-1 integration site selection. We propose that definitive sequence features such as the Alu-like motifs and SATB1-binding sites provide a unique chromatin context in vivo which is preferentially targeted by the HIV-1 integration machinery.
逆转录病毒整合最近被证明是非随机的,倾向于染色质的转录活性区域。然而,逆转录病毒选择整合位点的机制尚不清楚。我们在此表明,在报告的病毒整合位点侧翼序列中存在类似Alu的基序,这些序列与从人类基因组中随机挑选的序列显著不同,这表明人类免疫缺陷病毒1型(HIV-1)靶向的基因组区域存在独特的一级序列特征。此外,这些序列在体外和体内都优先被SATB1(T细胞谱系限制性染色质组织者)结合。Alu重复序列占人类基因组的近10%,并与转录调控有关。为了特异性分离病毒整合位点侧翼且同时含有类似Alu重复序列和SATB1结合位点的序列,我们将染色质免疫沉淀与连续PCR相结合。从HIV-1 NL4.3感染的Jurkat T细胞染色质中分离出的抗SATB1免疫沉淀基因组DNA片段池中,特异性免疫沉淀并扩增了HIV-1整合位点侧翼的克隆序列。此外,这些序列中的许多优先分布在与核基质紧密结合的DNA中,而不是在染色质环中。引人注目的是,当SATB1沉默时,这些区域中的许多对整合不利,这为其在HIV-1整合位点选择中的作用提供了明确证据。我们提出,诸如类似Alu的基序和SATB1结合位点等明确的序列特征在体内提供了一种独特的染色质环境,HIV-1整合机制优先靶向这种环境。