Rife Magalis Brittany, Kosakovsky Pond Sergei L, Summers Michael F, Salemi Marco
Emerging Pathogens Institute and Department of Pathology, Immunology and Laboratory Medicine, University of Florida, Gainesville, FL, USA.
Institute for Genomics and Evolutionary Medicine and Department of Biology, Temple University, Philadelphia, PA, USA.
Virus Evol. 2018 Jun 21;4(1):vey018. doi: 10.1093/ve/vey018. eCollection 2018 Jan.
Lentiviral RNA genomes contain structural elements that play critical roles in viral replication. Although structural features of 5'-untranslated regions have been well characterized, attempts to identify important structures in other genomic regions by Selective 2'-Hydroxyl Acylation analyzed by Primer Extension (SHAPE) have led to conflicting structural and mechanistic conclusions. Previous approaches accounted neither for sequence heterogeneity that is ubiquitous in viral populations, nor for selective constraints operating at the protein level. We developed an approach that augments SHAPE with phylogenetic analyses and applied it to investigate structure in coding regions (cRNA) within the HIV and SIV envelope genes. Analysis of single-genome SHAPE data with phylogenetic information from diverse lentiviral sequences argues against the conservation of a putative global RNA structure but points to the existence of core RNA sub-structures. Our findings establish a framework for considering sequence heterogeneity and protein function in RNA structure inference approaches.
慢病毒RNA基因组包含在病毒复制中起关键作用的结构元件。虽然5'非翻译区的结构特征已得到充分表征,但通过引物延伸分析的选择性2'-羟基酰化(SHAPE)来识别其他基因组区域中重要结构的尝试,得出了相互矛盾的结构和机制结论。以前的方法既没有考虑病毒群体中普遍存在的序列异质性,也没有考虑在蛋白质水平上起作用的选择性限制。我们开发了一种通过系统发育分析增强SHAPE的方法,并将其应用于研究HIV和SIV包膜基因编码区(cRNA)的结构。利用来自不同慢病毒序列的系统发育信息对单基因组SHAPE数据进行分析,结果表明不存在假定的全局RNA结构保守性,但指出存在核心RNA子结构。我们的研究结果建立了一个在RNA结构推断方法中考虑序列异质性和蛋白质功能的框架。