The dynamic nature of the four-way junction of the hepatitis C virus IRES

• Published in: RNA (Cambridge) 2003-07, Vol.9 (7), p.809-820
• Main Authors: Melcher, Sonya E, Wilson, Timothy J, Lilley, David M J
• Format: Article
• Language: English
• Subjects: Base Sequence; Hepacivirus - genetics; Kinetics; Models, Molecular; Molecular Sequence Data; Nucleic Acid Conformation; Protein Biosynthesis; Ribosomes - virology; RNA, Viral - chemistry; RNA, Viral - genetics; RNA, Viral - metabolism; Spectrometry, Fluorescence
• ISSN: 1355-8382; 1469-9001
• DOI: 10.1261/rna.5130703

Translation is initiated within the RNA of the hepatitis C virus at the internal ribosome entry site (IRES). The IRES is a 341-nucleotide element that contains a four-way helical junction (IIIabc) as a functionally important element of the secondary structure. The junction has three additional, nonpaired nucleotides at the point of strand exchange on one diagonal. We have studied the global conformation and folding of this junction in solution, using comparative gel electrophoresis and steady-state and time-resolved fluorescence resonance energy transfer. In the absence of divalent metal ions, the junction adopts an extended-square structure, in contrast to perfect four-way RNA junctions, which retain coaxial helical stacking under all conditions. The IIIabc junction is induced to fold on addition of Mg(2+), by pairwise coaxial stacking of arms, into the conformer in which the unpaired bases are located on the exchanging strands. Fluorescence lifetime measurements indicate that in the presence of Mg(2+) ions, the IIIabc junction exists in a dynamic equilibrium comprising approximately equal populations of antiparallel and parallel species. These dynamic properties may be important in mediating interactions between the IRES and the ribosome and initiation factors.