Transcription factor decoy oligonucleotides modified with locked nucleic acids: an in vitro study to reconcile biostability with binding affinity.
Identifieur interne : 000272 ( Ncbi/Checkpoint ); précédent : 000271; suivant : 000273Transcription factor decoy oligonucleotides modified with locked nucleic acids: an in vitro study to reconcile biostability with binding affinity.
Auteurs : Rita Crinelli [Italie] ; Marzia Bianchi ; Lucia Gentilini ; Linda Palma ; Mads D. S Rensen ; Torsten Bryld ; Ravindra B. Babu ; Khalil Arar ; Jesper Wengel ; Mauro MagnaniSource :
- Nucleic acids research [ 1362-4962 ] ; 2004.
Descripteurs français
- KwdFr :
- Cellules HeLa, Endonucleases (métabolisme), Exonucleases (métabolisme), Facteur de transcription NF-kappa B (métabolisme), Facteurs de transcription (métabolisme), Humains, Oligonucléotides, Oligonucléotides antisens (), Oligonucléotides antisens (métabolisme), Sites de fixation, Séquence consensus, Séquence nucléotidique.
- MESH :
English descriptors
- KwdEn :
- MESH :
- chemical , chemistry : Oligonucleotides, Antisense.
- chemical , metabolism : Endonucleases, Exonucleases, NF-kappa B, Oligonucleotides, Antisense, Transcription Factors.
- Base Sequence, Binding Sites, Consensus Sequence, HeLa Cells, Humans, Oligonucleotides.
Abstract
Double-stranded oligonucleotides (ODNs) containing the consensus binding sequence of a transcription factor provide a rationally designed tool to manipulate gene expression at the transcriptional level by the decoy approach. However, modifications introduced into oligonucleotides to increase stability quite often do not guarantee that transcription factor affinity and/or specificity of recognition are retained. We have previously evaluated the use of locked nucleic acids (LNA) in the design of decoy molecules for the transcription factor kappaB. Oligo nucleotides containing LNA substitutions displayed high resistance to exo- and endonucleolytic degradation, with LNA-DNA mix-mers being more stable than LNA-DNA-LNA gap-mers. However, insertion of internal LNA bases resulted in a loss of affinity for the transcription factor. This latter effect apparently depended on positioning of the internal LNA substitutions. Indeed, here we demonstrate that intra- and inter-strand positioning of internal LNAs has to be carefully considered to maintain affinity and achieve high stability, respectively. Unfortunately, our data also indicate that LNA positioning is not the only parameter affecting transcription factor binding, the interference in part being dependent on the intrinsic conformational properties of this nucleotide analog. To circumvent this problem, the successful use of an alpha-L-ribo- configured LNA is demonstrated, indicating LNA-DNA-alpha-L-LNA molecules as promising new decoy agents.
DOI: 10.1093/nar/gkh503
PubMed: 15051810
Affiliations:
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<term>Exonucleases (metabolism)</term>
<term>HeLa Cells</term>
<term>Humans</term>
<term>NF-kappa B (metabolism)</term>
<term>Oligonucleotides</term>
<term>Oligonucleotides, Antisense (chemistry)</term>
<term>Oligonucleotides, Antisense (metabolism)</term>
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<term>Oligonucleotides, Antisense</term>
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<front><div type="abstract" xml:lang="en">Double-stranded oligonucleotides (ODNs) containing the consensus binding sequence of a transcription factor provide a rationally designed tool to manipulate gene expression at the transcriptional level by the decoy approach. However, modifications introduced into oligonucleotides to increase stability quite often do not guarantee that transcription factor affinity and/or specificity of recognition are retained. We have previously evaluated the use of locked nucleic acids (LNA) in the design of decoy molecules for the transcription factor kappaB. Oligo nucleotides containing LNA substitutions displayed high resistance to exo- and endonucleolytic degradation, with LNA-DNA mix-mers being more stable than LNA-DNA-LNA gap-mers. However, insertion of internal LNA bases resulted in a loss of affinity for the transcription factor. This latter effect apparently depended on positioning of the internal LNA substitutions. Indeed, here we demonstrate that intra- and inter-strand positioning of internal LNAs has to be carefully considered to maintain affinity and achieve high stability, respectively. Unfortunately, our data also indicate that LNA positioning is not the only parameter affecting transcription factor binding, the interference in part being dependent on the intrinsic conformational properties of this nucleotide analog. To circumvent this problem, the successful use of an alpha-L-ribo- configured LNA is demonstrated, indicating LNA-DNA-alpha-L-LNA molecules as promising new decoy agents.</div>
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