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三种与HIV相关的RNA基因组的基于结构的比对和共有二级结构

Structure-Based Alignment and Consensus Secondary Structures for Three HIV-Related RNA Genomes.

作者信息

Lavender Christopher A, Gorelick Robert J, Weeks Kevin M

机构信息

Department of Chemistry, University of North Carolina, Chapel Hill, Chapel Hill, North Carolina, United States of America.

AIDS and Cancer Virus Program, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, Maryland, United States of America.

出版信息

PLoS Comput Biol. 2015 May 20;11(5):e1004230. doi: 10.1371/journal.pcbi.1004230. eCollection 2015 May.

Abstract

HIV and related primate lentiviruses possess single-stranded RNA genomes. Multiple regions of these genomes participate in critical steps in the viral replication cycle, and the functions of many RNA elements are dependent on the formation of defined structures. The structures of these elements are still not fully understood, and additional functional elements likely exist that have not been identified. In this work, we compared three full-length HIV-related viral genomes: HIV-1NL4-3, SIVcpz, and SIVmac (the latter two strains are progenitors for all HIV-1 and HIV-2 strains, respectively). Model-free RNA structure comparisons were performed using whole-genome structure information experimentally derived from nucleotide-resolution SHAPE reactivities. Consensus secondary structures were constructed for strongly correlated regions by taking into account both SHAPE probing structural data and nucleotide covariation information from structure-based alignments. In these consensus models, all known functional RNA elements were recapitulated with high accuracy. In addition, we identified multiple previously unannotated structural elements in the HIV-1 genome likely to function in translation, splicing and other replication cycle processes; these are compelling targets for future functional analyses. The structure-informed alignment strategy developed here will be broadly useful for efficient RNA motif discovery.

摘要

人类免疫缺陷病毒(HIV)及相关的灵长类慢病毒拥有单链RNA基因组。这些基因组的多个区域参与病毒复制周期中的关键步骤,并且许多RNA元件的功能取决于特定结构的形成。这些元件的结构仍未被完全理解,可能还存在尚未被识别的其他功能元件。在这项研究中,我们比较了三种全长HIV相关病毒基因组:HIV-1 NL4-3、黑猩猩猴免疫缺陷病毒(SIVcpz)和恒河猴猴免疫缺陷病毒(SIVmac)(后两种毒株分别是所有HIV-1和HIV-2毒株的祖先)。使用从核苷酸分辨率的SHAPE反应性实验得出的全基因组结构信息进行无模型RNA结构比较。通过综合考虑SHAPE探测结构数据和基于结构比对的核苷酸共变信息,为强相关区域构建了共有二级结构。在这些共有模型中,所有已知的功能性RNA元件都被高精度地重现。此外,我们在HIV-1基因组中鉴定出多个先前未注释的结构元件,它们可能在翻译、剪接和其他复制周期过程中发挥作用;这些是未来功能分析的引人注目的靶点。这里开发的基于结构的比对策略将广泛用于高效的RNA基序发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c496/4439019/d9b907371649/pcbi.1004230.g001.jpg

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