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不同 HIV-1 毒株 5'长末端重复 U3 区的独特变异。

Distinctive variation in the U3R region of the 5' Long Terminal Repeat from diverse HIV-1 strains.

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, Maryland, United States of America.

Department of Molecular Biology, Faculty of Medicine, Pharmacy and Biomedical sciences, University of Douala, Douala, Cameroon.

出版信息

PLoS One. 2018 Apr 17;13(4):e0195661. doi: 10.1371/journal.pone.0195661. eCollection 2018.

DOI:10.1371/journal.pone.0195661
PMID:29664930
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5903597/
Abstract

Functional mapping of the 5'LTR has shown that the U3 and the R regions (U3R) contain a cluster of regulatory elements involved in the control of HIV-1 transcription and expression. As the HIV-1 genome is characterized by extensive variability, here we aimed to describe mutations in the U3R from various HIV-1 clades and CRFs in order to highlight strain specific differences that may impact the biological properties of diverse HIV-1 strains. To achieve our purpose, the U3R sequence of plasma derived virus belonging to different clades (A1, B, C, D, F2) and recombinants (CRF02_AG, CRF01_AE and CRF22_01A1) was obtained using Illumina technology. Overall, the R region was very well conserved among and across different strains, while in the U3 region the average inter-strains nucleotide dissimilarity was up to 25%. The TAR hairpin displayed a strain-distinctive cluster of mutations affecting the bulge and the loop, but mostly the stem. Like in previous studies we found a TATAA motif in U3 promoter region from the majority of HIV-1 strains and a TAAAA motif in CRF01_AE; but also in LTRs from CRF22_01A1 isolates. Although LTRs from CRF22_01A1 specimens were assigned CRF01_AE, they contained two NF-kB sites instead of the single TFBS described in CRF01_AE. Also, as previously describe in clade C isolates, we found no C/EBP binding site directly upstream of the enhancer region in CRF22_01A1 specimens. In our study, one-third of CRF02_AG LTRs displayed three NF-kB sites which have been mainly described in clade C isolates. Overall, the number, location and binding patterns of potential regulatory elements found along the U3R might be specific to some HIV-1 strains such as clade F2, CRF02_AG, CRF01_AE and CRF22_01A1. These features may be worth consideration as they may be involved in distinctive regulation of HIV-1 transcription and replication by different and diverse infecting strains.

摘要

5'LTR 的功能图谱显示,U3 和 R 区(U3R)包含一组参与 HIV-1 转录和表达调控的调节元件。由于 HIV-1 基因组具有广泛的变异性,因此我们旨在描述来自不同 HIV-1 谱系和 CRF 的 U3R 中的突变,以突出可能影响不同 HIV-1 株生物学特性的菌株特异性差异。为了达到我们的目的,使用 Illumina 技术获得了属于不同谱系(A1、B、C、D、F2)和重组体(CRF02_AG、CRF01_AE 和 CRF22_01A1)的血浆衍生病毒的 U3R 序列。总体而言,R 区在不同株之间非常保守,而在 U3 区,株间核苷酸差异的平均值高达 25%。TAR 发夹显示出一个菌株特有的突变簇,影响了凸起和环,但主要是茎。与之前的研究一样,我们在大多数 HIV-1 株的 U3 启动子区域发现了一个 TATAA 基序,在 CRF01_AE 中发现了一个 TAAAA 基序;但在 CRF22_01A1 分离株的 LTR 中也发现了这一基序。尽管 CRF22_01A1 标本的 LTR 被分配为 CRF01_AE,但它们包含两个 NF-kB 位点,而不是 CRF01_AE 中描述的单个 TFBS。此外,正如在 C 谱系分离株中所描述的,我们在 CRF22_01A1 标本的增强子区域上游没有发现直接的 C/EBP 结合位点。在我们的研究中,三分之一的 CRF02_AG LTR 显示出三个 NF-kB 位点,这些位点主要在 C 谱系分离株中描述。总体而言,U3R 沿线发现的潜在调节元件的数量、位置和结合模式可能是特定于某些 HIV-1 株的,如 F2 谱系、CRF02_AG、CRF01_AE 和 CRF22_01A1。这些特征可能值得考虑,因为它们可能参与不同和多样化的感染株对 HIV-1 转录和复制的独特调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a66a/5903597/651358c4aab5/pone.0195661.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a66a/5903597/0b894a92517b/pone.0195661.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a66a/5903597/b8eb4f4588d7/pone.0195661.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a66a/5903597/651358c4aab5/pone.0195661.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a66a/5903597/0b894a92517b/pone.0195661.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a66a/5903597/b8eb4f4588d7/pone.0195661.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a66a/5903597/651358c4aab5/pone.0195661.g003.jpg

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