Structural and Functional Characterization of Programmed Ribosomal Frameshift Signals in West Nile Virus Strains Reveals High Structural Plasticity Among cis-Acting RNA Elements

التفاصيل البيبلوغرافية
العنوان: Structural and Functional Characterization of Programmed Ribosomal Frameshift Signals in West Nile Virus Strains Reveals High Structural Plasticity Among cis-Acting RNA Elements
المؤلفون: Sharmishtha Musalgaonkar, John E. Jones, Jonathan D. Dinman, Yousuf A. Khan, Christine A. Moomau
المصدر: Journal of Biological Chemistry
سنة النشر: 2016
مصطلحات موضوعية: 0301 basic medicine, viruses, 030106 microbiology, Viral quasispecies, Biology, Viral Nonstructural Proteins, Biochemistry, Ribosome, Models, Biological, Ribosomal frameshift, Frameshift mutation, 03 medical and health sciences, RNA, Messenger, Nucleic acid structure, Molecular Biology, Genetics, Translational frameshift, RNA, virus diseases, Frameshifting, Ribosomal, Cell Biology, digestive system diseases, 030104 developmental biology, RNA, Viral, Pseudoknot, West Nile virus
الوصف: West Nile virus (WNV) is a prototypical emerging virus for which no effective therapeutics currently exist. WNV uses programmed -1 ribosomal frameshifting (-1 PRF) to synthesize the NS1' protein, a C terminally extended version of its non-structural protein 1, the expression of which enhances neuro-invasiveness and viral RNA abundance. Here, the NS1' frameshift signals derived from four WNV strains were investigated to better understand -1 PRF in this quasispecies. Sequences previously predicted to promote -1 PRF strongly promote this activity, but frameshifting was significantly more efficient upon inclusion of additional 3' sequence information. The observation of different rates of -1 PRF, and by inference differences in the expression of NS1', may account for the greater degrees of pathogenesis associated with specific WNV strains. Chemical modification and mutational analyses of the longer and shorter forms of the -1 PRF signals suggests dynamic structural rearrangements between tandem stem-loop and mRNA pseudoknot structures in two of the strains. A model is suggested in which this is employed as a molecular switch to fine tune the relative expression of structural to non-structural proteins during different phases of the viral replication cycle.
تدمد: 1083-351X
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afd85985fd7afb5e7c3640142f2a6896
https://pubmed.ncbi.nlm.nih.gov/27226636
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....afd85985fd7afb5e7c3640142f2a6896
قاعدة البيانات: OpenAIRE