The effect of RNA secondary structures on RNA-ligand binding and the modifier RNA mechanism: a quantitative model

RNA-ligand binding often depends crucially on the local RNA secondary structure at the binding site. We develop here a model that quantitatively predicts the effect of RNA secondary structure on effective RNA-ligand binding activities based on equilibrium thermodynamics and the explicit computations of partition functions for the RNA structures. A statistical test for the impact of a particular structural feature on the binding affinities follows directly from this approach. The formalism is extended to describing the effects of hybridizing small “modifier RNAs” to a target RNA molecule outside its ligand binding site. We illustrate the applicability of our approach by quantitatively describing the interaction of the mRNA stabilizing protein HuR with AU-rich elements [Meisner, N.-C., Hackermüller, J., Uhl, V., Aszódi, A., Jaritz, M., Auer, M., 2004. mRNA openers and closers: a methodology to modulate AU-rich element controlled mRNA stability by a molecular switch in mRNA conformation. ChemBioChem 5, 1432-1447]. We discuss our model and recent experimental findings demonstrating the effectivity of modifier RNAs in vitro in the context of the current research activities in the field of non-coding RNAs. We speculate that modifier RNAs might also exist in nature; if so, they present an additional regulatory layer for fine-tuning gene expression that could evolve rapidly, leaving no obvious traces in the genomic DNA sequences.