Single-Molecule FRET Reveals Three Conformations for the TLS Domain of Brome Mosaic Virus Genome

• Published in: Biophysical journal Vol. 109; no. 12; pp. 2625 - 2636
• Main Authors: Vieweger, Mario, Holmstrom, Erik D., Nesbitt, David J.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 15-12-2015; Biophysical Society; The Biophysical Society
• Subjects: Base Sequence; Bromovirus; Diffusion; Fluorescence Resonance Energy Transfer; Gene expression; Metals - pharmacology; Models, Molecular; Molecules; Nucleic Acid Conformation; Proteins and Nucleic Acids; Ribonucleic acid; Riboswitch - drug effects; RNA; RNA, Transfer - chemistry; RNA, Viral - chemistry; RNA, Viral - genetics; Thermodynamics; Viruses
• ISSN: 0006-3495; 1542-0086
• DOI: 10.1016/j.bpj.2015.10.006

Metabolite-dependent conformational switching in RNA riboswitches is now widely accepted as a critical regulatory mechanism for gene expression in bacterial systems. More recently, similar gene regulation mechanisms have been found to be important for viral systems as well. One of the most abundant and best-studied systems is the tRNA-like structure (TLS) domain, which has been found to occur in many plant viruses spread across numerous genera. In this work, folding dynamics for the TLS domain of Brome Mosaic Virus have been investigated using single-molecule fluorescence resonance energy transfer techniques. In particular, burst fluorescence methods are exploited to observe metal-ion ([Mn+])-induced folding in freely diffusing RNA constructs resembling the minimal TLS element of brome mosaic virus RNA3. The results of these experiments reveal a complex equilibrium of at least three distinct populations. A stepwise, or consecutive, thermodynamic model for TLS folding is developed, which is in good agreement with the [Mn+]-dependent evolution of conformational populations and existing structural information in the literature. Specifically, this folding pathway explains the metal-ion dependent formation of a functional TLS domain from unfolded RNAs via two consecutive steps: 1) hybridization of a long-range stem interaction, followed by 2) formation of a 3′-terminal pseudoknot. These two conformational transitions are well described by stepwise dissociation constants for [Mg2+] (K1 = 328 ± 30 μM and K2 = 1092 ± 183 μM) and [Na+] (K1 = 74 ± 6 mM and K2 = 243 ± 52 mM)-induced folding. The proposed thermodynamic model is further supported by inhibition studies of the long-range stem interaction using a complementary DNA oligomer, which effectively shifts the dynamic equilibrium toward the unfolded conformation. Implications of this multistep conformational folding mechanism are discussed with regard to regulation of virus replication.