Document Detail

Targeting of antisense PNA oligomers to human galanin receptor type 1 mRNA.
MedLine Citation:
PMID:  15464198     Owner:  NLM     Status:  MEDLINE    
In this work, we have targeted positions 18-38 of the human galanin receptor type 1 (GalR1) mRNA coding sequence with different peptide nucleic acid (PNA) oligomers. This region has previously been shown to be a good antisense region and therefore we aimed to identify the subregions and/or thermodynamic parameters determining the antisense efficacy. Nine different PNA oligomers were conjugated to a cell-penetrating peptide, transportan, to enhance their cellular uptake. Concentration-dependent down-regulation of GalR1 protein expression in human melanoma cell line Bowes was measured by radioligand binding assay. No reduction of GalR1 mRNA level was observed upon PNA treatment, thus, the effect was concluded to be translational arrest. Judging from the EC50 values, antisense PNA oligomers targeting regions 24-38 (EC50=70 nM) or 27-38 (EC50=80 nM) were the most potent suppressors of protein expression. No parameter predicted by M-fold algorithm was found to correlate with the measured antisense activities. Presence of some subregions was found not to increase antisense efficiency of PNA. Presence of a short unpaired triplet between nucleotides 33 and 35 in the target region was, on the other hand, found to be the most critical for efficient GalR1 down-regulation. Thus, the results are of high impact in designing antisense oligomers. Specific results of this study demonstrate 20-fold more efficient antisense down-regulation of GalR1 as achieved before.
Kalle Kilk; Anna Elmquist; Külliki Saar; Margus Pooga; Tiit Land; Tamas Bartfai; Ursel Soomets; Ulo Langel
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Neuropeptides     Volume:  38     ISSN:  0143-4179     ISO Abbreviation:  Neuropeptides     Publication Date:  2004 Oct 
Date Detail:
Created Date:  2004-10-06     Completed Date:  2005-03-29     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  8103156     Medline TA:  Neuropeptides     Country:  Scotland    
Other Details:
Languages:  eng     Pagination:  316-24     Citation Subset:  IM    
Department of Neurochemistry and Neurotoxicology, Arrhenius Laboratories, Stockholm University, Svante Arrheniusvag. 21A, S-10691 Stockholm, Sweden.
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MeSH Terms
Cell Line, Tumor
Nucleic Acid Conformation
Oligonucleotides, Antisense / genetics,  metabolism*
Peptide Nucleic Acids / genetics,  metabolism*
RNA, Messenger / chemistry,  genetics,  metabolism*
Receptor, Galanin, Type 1 / genetics*,  metabolism
Reg. No./Substance:
0/Oligonucleotides, Antisense; 0/Peptide Nucleic Acids; 0/RNA, Messenger; 0/Receptor, Galanin, Type 1

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