📄 A conserved RNA pseudoknot in a putative molecular switch domain of the 3′-untranslated region of coronaviruses is only marginally stable

The 3′-untranslated region (UTR) of the group 2 coronavirus mouse hepatitis virus (MHV) genome contains a predicted bulged stem-loop (designated P0ab), a conserved cis-acting pseudoknot (PK), and a more distal stem-loop (designated P2). Base-pairing to create the pseudoknot-forming stem (P1pk) is mutually exclusive with formation of stem P0a at the base of the bulged stem-loop; as a result, the two structures cannot be present simultaneously. Herein, we use thermodynamic methods to evaluate the ability of individual subdomains of the 3′ UTR to adopt a pseudoknotted conformation. We find that an RNA capable of forming only the predicted PK (58 nt; 3′ nucleotides 241-185) adopts the P2 stem-loop with little evidence for P1pk pairing in 0.1 M KCl and the absence of Mg2+; as Mg2+ or 1 M KCl is added, a new thermal unfolding transition is induced and assignable to P1pkpairing. The P1pk helix is only marginally stable, ΔG25 ≈ 1.2 ± 0.3 kcal/mol (5.0 mM Mg2+, 100 mM K+), and unfolded at 37° C. Similar findings characterize an RNA 5′ extended through the P0b helix only (89 nt; 294-185). In contrast, an RNA capable of forming either the P0a helix or the pseudoknot (97 nt; 301-185) forms no P1pk helix. Thermal unfolding simulations are fully consistent with these experimental findings. These data reveal that the PK forms weakly and only when the competing double-hairpin structure cannot form; in the UTR RNA, the double hairpin is the predominant conformer under all solution conditions. Published by Cold Spring Harbor Laboratory Press. Copyright © 2011 RNA Society.

keywords 🔗 hepatitis virus (437) 🔗 coronavirus mouse (66) 🔗 mouse hepatitis (371)

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