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主要 HIV-1 亚型和循环重组形式的 U5 和下游序列的遗传变异性。

Genetic variability of the U5 and downstream sequence of major HIV-1 subtypes and circulating recombinant forms.

机构信息

Laboratory of Molecular Virology, Division of Emerging and Transfusion Transmitted Diseases, Center for Biologics Evaluation and Research, Food and Drug Administration, Silver Spring, MD, USA.

Laboratory of Molecular Virology, Division of Emerging and Transfusion Transmitted Diseases, Center for Biologics Evaluation and Research, Food and Drug Administration, Building 72, Rm 4230 10903 New Hampshire Avenue, Silver Spring, MD, 20993, USA.

出版信息

Sci Rep. 2020 Aug 6;10(1):13214. doi: 10.1038/s41598-020-70083-1.

Abstract

The critical role of the regulatory elements at the 5' end of the HIV-1 genome in controlling the life cycle of HIV-1 indicates that this region significantly influences virus fitness and its biological properties. In this study, we performed a detailed characterization of strain-specific variability of sequences from the U5 to upstream of the gag gene start codon of diverse HIV-1 strains by using next-generation sequencing (NGS) techniques. Overall, we found that this region of the HIV-1 genome displayed a low degree of intra-strain variability. On the other hand, inter-strain variability was found to be as high as that reported for gag and env genes (13-17%). We observed strain-specific single point and clustered mutations in the U5, PBS, and gag leader sequences (GLS), generating potential strain-specific transcription factor binding sites (TFBS). Using an infrared gel shift assay, we demonstrated the presence of potential TFBS such as E-box in CRF22_01A, and Stat 6 in subtypes A and G, as well as in their related CRFs. The strain-specific variation found in the sequence corresponding at the RNA level to functional domains of the 5' UTR, could also potentially impact the secondary/tertiary structural rearrangement of this region. Thus, the variability observed in this 5' end of the genomic region of divergent HIV-1 strains strongly suggests that functions of this region might be affected in a strain-specific manner. Our findings provide new insights into DNA-protein interactions that regulate HIV-1 replication and the influence of strain characterization on the biology of HIV-1 infection.

摘要

HIV-1 基因组 5' 端调控元件在控制 HIV-1 生命周期中的关键作用表明,该区域显著影响病毒适应性及其生物学特性。在这项研究中,我们使用下一代测序(NGS)技术,对不同 HIV-1 毒株 U5 至 gag 基因起始密码子上游的序列进行了详细的特征分析。总的来说,我们发现 HIV-1 基因组的这一区域显示出低度的株内变异性。另一方面,株间变异性与 gag 和 env 基因报道的变异性一样高(13-17%)。我们观察到 U5、PBS 和 gag 前导序列(GLS)中存在株特异性的单点和簇状突变,产生潜在的株特异性转录因子结合位点(TFBS)。通过红外凝胶迁移实验,我们证明了 CRF22_01A 中的 E-box 以及 A 和 G 亚型中的 Stat 6 以及它们相关的 CRFs 中存在潜在的 TFBS。在 RNA 水平上与 5'UTR 功能域相对应的序列中发现的株间差异,也可能潜在地影响该区域的二级/三级结构重排。因此,在不同 HIV-1 毒株的基因组区域 5' 端观察到的变异性强烈表明,该区域的功能可能以株特异性的方式受到影响。我们的发现为调节 HIV-1 复制的 DNA-蛋白相互作用以及株特征分析对 HIV-1 感染生物学的影响提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/def7/7411029/5bbf305950b8/41598_2020_70083_Fig1_HTML.jpg

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