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伪狂犬病毒基因组中 G₂-四链体的密集分布及其对阳离子和 G-四链体配体的敏感性。

Intensive Distribution of G₂-Quaduplexes in the Pseudorabies Virus Genome and Their Sensitivity to Cations and G-Quadruplex Ligands.

机构信息

Laboratory of Medicinal Biophysical Chemistry, College of Science, Huazhong Agricultural University, Wuhan 430070, China.

Hubei Key Laboratory of Agricultural Bioinformatics, College of Informatics, Huazhong Agricultural University, Wuhan 430070, China.

出版信息

Molecules. 2019 Feb 21;24(4):774. doi: 10.3390/molecules24040774.

DOI:10.3390/molecules24040774
PMID:30795541
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6412908/
Abstract

Guanine-rich sequences in the genomes of herpesviruses can fold into G-quadruplexes. Compared with the widely-studied G₃-quadruplexes, the dynamic G₂-quadruplexes are more sensitive to the cell microenvironment, but they attract less attention. Pseudorabies virus (PRV) is the model species for the study of the latency and reactivation of herpesvirus in the nervous system. A total of 1722 G₂-PQSs and 205 G₃-PQSs without overlap were identified in the PRV genome. Twelve G₂-PQSs from the CDS region exhibited high conservation in the genomes of the genus. Eleven G₂-PQSs were 100% conserved in the repeated region of the annotated PRV genomes. There were 212 non-redundant G₂-PQSs in the 3' UTR and 19 non-redundant G₂-PQSs in the 5' UTR, which would mediate gene expression in the post-transcription and translation processes. The majority of examined G₂-PQSs formed parallel structures and exhibited different sensitivities to cations and small molecules in vitro. Two G₂-PQSs, respectively, from 3' UTR of (encoding helicase motif) and (encoding sequence-specific ori-binding protein) exhibited diverse regulatory activities with/without specific ligands in vivo. The G-quadruplex ligand, NMM, exhibited a potential for reducing the virulence of the PRV Ea strain. The systematic analysis of the distribution of G₂-PQSs in the PRV genomes could guide further studies of the G-quadruplexes' functions in the life cycle of herpesviruses.

摘要

富含鸟嘌呤的序列可以在疱疹病毒的基因组中折叠成 G-四链体。与广泛研究的 G₃-四链体相比,动态 G₂-四链体对细胞微环境更敏感,但受到的关注较少。伪狂犬病病毒(PRV)是研究疱疹病毒在神经系统中潜伏和再激活的模式物种。在 PRV 基因组中总共鉴定出 1722 个无重叠的 G₂-PQS 和 205 个 G₃-PQS。来自 CDS 区的 12 个 G₂-PQS 在属的基因组中表现出高度保守。11 个 G₂-PQS 在注释的 PRV 基因组重复区中 100%保守。在 3'UTR 中有 212 个非冗余的 G₂-PQS 和在 5'UTR 中有 19 个非冗余的 G₂-PQS,它们将在转录后和翻译过程中调节基因表达。大多数检查的 G₂-PQS 形成平行结构,在体外对阳离子和小分子表现出不同的敏感性。来自 3'UTR 的两个 G₂-PQS,分别编码解旋酶基序和序列特异性 ori 结合蛋白,在体内具有/没有特定配体时表现出不同的调节活性。G-四链体配体 NMM 表现出降低 PRV Ea 株毒力的潜力。对 PRV 基因组中 G₂-PQS 分布的系统分析可以指导进一步研究 G-四链体在疱疹病毒生命周期中的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7296/6412908/caf4ad7b7650/molecules-24-00774-g011.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7296/6412908/509d04df8a97/molecules-24-00774-g009a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7296/6412908/bda6b4d77e46/molecules-24-00774-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7296/6412908/caf4ad7b7650/molecules-24-00774-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7296/6412908/0261a9a5c58e/molecules-24-00774-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7296/6412908/e6794f6bed7a/molecules-24-00774-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7296/6412908/fa1b3f82c2f7/molecules-24-00774-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7296/6412908/24457f3f931f/molecules-24-00774-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7296/6412908/218de00eab24/molecules-24-00774-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7296/6412908/f5707777521b/molecules-24-00774-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7296/6412908/6cc276d1ea13/molecules-24-00774-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7296/6412908/38a69f1b7441/molecules-24-00774-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7296/6412908/bda6b4d77e46/molecules-24-00774-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7296/6412908/caf4ad7b7650/molecules-24-00774-g011.jpg

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