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丁型肝炎病毒基因组中富含形成G-四链体的序列。

Abundance of G-Quadruplex Forming Sequences in the Hepatitis Delta Virus Genomes.

作者信息

Brázda Václav, Valková Natália, Dobrovolná Michaela, Mergny Jean-Louis

机构信息

Institute of Biophysics of the Czech Academy of Sciences, Královopolská 135, Brno 621 00, Czech Republic.

Faculty of Chemistry, Brno University of Technology, Purkyňova 118, Brno 61200, Czech Republic.

出版信息

ACS Omega. 2024 Jan 9;9(3):4096-4101. doi: 10.1021/acsomega.3c09288. eCollection 2024 Jan 23.

Abstract

Hepatitis delta virus (HDV) is a highly unusual RNA satellite virus that depends on the presence of hepatitis B virus (HBV) to be infectious. Its compact and variable single-stranded RNA genome consists of eight major genotypes distributed unevenly across different continents. The significance of noncanonical secondary structures such as G-quadruplexes (G4s) is increasingly recognized at the DNA and RNA levels, particularly for transcription, replication, and translation. G4s are formed from guanine-rich sequences and have been identified in the vast majority of viral, eukaryotic, and prokaryotic genomes. In this study, we analyzed the G4 propensity of HDV genomes by using G4Hunter. Unlike HBV, which has a G4 density similar to that of the human genome, HDV displays a significantly higher number of potential quadruplex-forming sequences (PQS), with a density more than four times greater than that of the human genome. This finding suggests a critical role for G4s in HDV, especially given that the PQS regions are conserved across HDV genotypes. Furthermore, the prevalence of G4-forming sequences may represent a promising target for therapeutic interventions to control HDV replication.

摘要

丁型肝炎病毒(HDV)是一种非常特殊的RNA卫星病毒,其具有传染性依赖于乙型肝炎病毒(HBV)的存在。其紧凑且可变的单链RNA基因组由八个主要基因型组成,在不同大陆分布不均。非经典二级结构如G-四链体(G4s)在DNA和RNA水平上的重要性日益得到认可,特别是在转录、复制和翻译方面。G4s由富含鸟嘌呤的序列形成,已在绝大多数病毒、真核生物和原核生物基因组中被鉴定出来。在本研究中,我们使用G4Hunter分析了HDV基因组的G4倾向。与HBV的G4密度与人基因组相似不同,HDV显示出显著更多的潜在四链体形成序列(PQS),其密度比人基因组高出四倍多。这一发现表明G4s在HDV中起关键作用,特别是考虑到PQS区域在HDV各基因型中是保守的。此外,形成G4的序列的普遍性可能代表了控制HDV复制的治疗干预的一个有前景的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf5c/10809645/7ac3d6db8957/ao3c09288_0001.jpg

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