RNA: a Publication of the RNA Society

Publication date: 2009-12
Volume: 15 Pages: 2195 - 2205
ISSN: 1355-8382, 1469-9001 PMID: 19850914
DOI: 10.1261/rna.1747509
Publisher: Cambridge University Press


Chu, Vincent B
Lipfert, Jan ; Bai, Yu ; Pande, Vijay S ; Doniach, Sebastian ; Herschlag, Daniel


electrostatics, folding, junctions, thermodynamics, Science & Technology, Life Sciences & Biomedicine, Biochemistry & Molecular Biology, TETRAHYMENA RIBOZYME, TERTIARY STRUCTURE, ELECTROSTATICS, SCATTERING, LANDSCAPE, DYNAMICS, PATHWAY, BINDING, EVENTS, Models, Molecular, Nucleic Acid Conformation, RNA, RNA Stability, Static Electricity, Thermodynamics, 0601 Biochemistry and Cell Biology, Developmental Biology


Structured RNAs must fold into their native structures and discriminate against a large number of alternative ones, an especially difficult task given the limited information content of RNA's nucleotide alphabet. The simplest motifs within structured RNAs are two helices joined by nonhelical junctions. To uncover the fundamental behavior of these motifs and to elucidate the underlying physical forces and challenges faced by structured RNAs, we computationally and experimentally studied a tethered duplex model system composed of two helices joined by flexible single- or double-stranded polyethylene glycol tethers, whose lengths correspond to those typically observed in junctions from structured RNAs. To dissect the thermodynamic properties of these simple motifs, we computationally probed how junction topology, electrostatics, and tertiary contact location influenced folding stability. Small-angle X-ray scattering was used to assess our predictions. Single- or double-stranded junctions, independent of sequence, greatly reduce the space of allowed helical conformations and influencing the preferred location and orientation of their adjoining helices. A double-stranded junction guides the helices along a hinge-like pathway. In contrast, a single-stranded junction samples a broader set of conformations and has different preferences than the double-stranded junction. In turn, these preferences determine the stability and distinct specificities of tertiary structure formation. These sequence-independent effects suggest that properties as simple as a junction's topology can generally define the accessible conformational space, thereby stabilizing desired structures and assisting in discriminating against misfolded structures. Thus, junction topology provides a fundamental strategy for transcending the limitations imposed by the low information content of RNA primary sequence.