Carregant...
Miniatura

Tipus de document

Article

Versió

Versió publicada

Data de publicació

Llicència de publicació

cc-by (c) Alagia, Adele et al., 2014
Si us plau utilitzeu sempre aquest identificador per citar o enllaçar aquest document: https://hdl.handle.net/2445/179418

RANA/aTNA chimeras: RNAi effects and nuclease resistance of single and double-stranded RNAs

Títol de la revista

Director/Tutor

ISSN de la revista

Títol del volum

Resum

The RNA interference pathway (RNAi) is a specific and powerful biological process, triggered by small non-coding RNA molecules and involved in gene expression regulation. In this work, we explored the possibility of increasing the biological stability of these RNA molecules by replacing their natural ribose ring with an acyclic L-threoninol backbone. In particular, this modification has been incorporated at certain positions of the oligonucleotide strands and its effects on the biological properties of the siRNA have been evaluated. In vitro cellular RNAi assays have demonstrated that the L-threoninol backbone is well tolerated by the RNAi machinery in both double and single-stranded fashion, with activities significantly higher than those evinced by the unmodified RNAs and comparable to the well-known phosphorothioate modification. Additionally, this modification conferred extremely strong resistance to serum and 3'/5'-exonucleases. In view of these results, we applied this modification to the knockdown of a therapeutically relevant human gene such as apolipoprotein B (ApoB). Further studies on the activation of the innate immune system showed that L-threoninol-modified RNAs are slightly less stimulatory than unmodified RNAs.

Citació

Citació

ALAGIA, Adele, TERRAZAS MARTÍNEZ, Montserrat, ERITJA I CASADELLÀ, Ramon. RANA/aTNA chimeras: RNAi effects and nuclease resistance of single and double-stranded RNAs. _Molecules_. 2014. Vol. 19, núm. 11, pàgs. 17872-17896. [consulta: 25 de febrer de 2026]. ISSN: 1420-3049. [Disponible a: https://hdl.handle.net/2445/179418]

Exportar metadades

JSON - METS

Compartir registre