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Antisense gene inhibition by oligonucleotides containing C-5 propyne pyrimidines.
- Source :
-
Science (New York, N.Y.) [Science] 1993 Jun 04; Vol. 260 (5113), pp. 1510-3. - Publication Year :
- 1993
-
Abstract
- Phosphorothioate oligodeoxynucleotides containing the C-5 propyne analogs of uridine and cytidine bind RNA with high affinity and are potent antisense inhibitors of gene expression. In a cellular assay, gene-specific antisense inhibition occurred at nanomolar concentrations of oligonucleotide, was dose-dependent and exquisitely sensitive to sequence mismatches, and was correlated with the melting temperature and length of oligonucleotide. Activity was independent of RNA target site and cell type but was detectable only when the oligonucleotides were microinjected or delivered with cell-permeabilizing agents. These oligonucleotides may have important applications in therapy and in studies of gene function.
- Subjects :
- Alkynes pharmacology
Animals
Base Sequence
Cell Line
Chlorocebus aethiops
Humans
Molecular Sequence Data
Oligonucleotides, Antisense pharmacokinetics
Pyrimidine Nucleotides pharmacokinetics
Rats
Thionucleotides pharmacokinetics
Oligonucleotides, Antisense pharmacology
Pyrimidine Nucleotides pharmacology
RNA drug effects
Thionucleotides pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0036-8075
- Volume :
- 260
- Issue :
- 5113
- Database :
- MEDLINE
- Journal :
- Science (New York, N.Y.)
- Publication Type :
- Academic Journal
- Accession number :
- 7684856
- Full Text :
- https://doi.org/10.1126/science.7684856