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Short Communication |
1 Servicio de Medicina Interna-Hepatología, Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, 08035 Barcelona, Spain
2 Department of Biochemistry, Weill Medical College of Cornell University, New York, NY 10021, USA
Correspondence
Jordi Gómez
jgomez{at}hg.vhebron.es
Accessibility to folded RNA and low potential of variation in the target RNA are crucial requirements for ribozyme therapy against virus infections. In hepatitis C virus (HCV), the sequence of the 5'UTR is conserved but the highly folded RNA structure severely limits the number of accessible sites. To expand investigation of targeting in the HCV genome, we have considered an internal genomic region whose sequence variation has been widely investigated and which has a particularly conserved RNA structure, which makes it accessible to the human RNase P in vitro. We have first mapped the accessibility of the genomic RNA to complementary DNAs within this internal genomic region. We performed a kinetic and thermodynamic study. Accordingly, we have designed and assayed four RNase P M1 RNA guide sequence ribozymes targeted to the selected sites. Considerations of RNA structural accessibility and sequence variation indicate that several target sites should be defined for simultaneous attack.
Published ahead of print on 31 March 2003 as DOI 10.1099/vir.0.18898-0.
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M. Martell, C. Briones, A. de Vicente, M. Piron, J. I. Esteban, R. Esteban, J. Guardia, and J. Gomez Structural analysis of hepatitis C RNA genome using DNA microarrays Nucleic Acids Res., June 24, 2004; 32(11): e90 - e90. [Abstract] [Full Text] [PDF] |
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