Organic & Biomolecular Chemistry · 2012 · 17 citations · 39 references
Life SciencesChemical BiologyMolecular BiologyNucleic Acid BiochemistryNucleic Acid ChemistryRna BiologyNucleic Acid SynthesisRibonucleic Acid (Rna) ChemistryRna EngineeringRna InterferenceRna ModificationRna StructureAlkyne Cycloaddition ReactionsChemical Modification Of Small Interfering Ribonucleic AcidsCycloaddition ReactionsDuplex StabilityRna Base PairingRna Duplex StabilitySmall Interfering Ribonucleic Acids (Sirnas)Small Interfering Rna (Sirna) Chemistry
Here we describe the synthesis of new 7-substituted 8-aza-7-deazaadenosine ribonucleoside phosphoramidites and their use in generating major groove-modified duplex RNAs. A 7-ethynyl analog leads to further structural diversification of the RNA via post-automated RNA synthesis azide-alkyne cycloaddition reactions. In addition, we report preliminary studies on the effects of eight different purine 7-position modifications on RNA duplex stability and pairing specificity. Finally, the effect on RNAi activity of this type of modification at eight different positions in an siRNA guide strand has been explored. Analogs were identified with large 7-position substituents that maintain adenosine pairing specificity and are well-tolerated at specific positions in an siRNA guide strand.
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MicroRNA Targeting Specificity in Mammals: Determinants beyond Seed Pairing
Andrew Grimson, Kyle Kai‐How Farh, Wendy K. Johnston et al. · Molecular Cell · 2007 · 3.8K citations · Full text