In vitro and in vivo action of antisense RNA
Identifieur interne : 001114 ( Istex/Curation ); précédent : 001113; suivant : 001115In vitro and in vivo action of antisense RNA
Auteurs : Wolfgang Nellen [Allemagne] ; Georg Sczakiel [Allemagne]Source :
- Molecular Biotechnology [ 1073-6085 ] ; 1996-08-01.
English descriptors
- KwdEn :
- Teeft :
- Annealing, Antisense, Antisense machinery, Antisense mechanisms, Antisense rnas, Antisense transcripts, Artificial antisense, Biol, Cellular proteins, Complementary sequences, Complementary strands, Degradation, Dictyostelium, Dsrna, Duplex, Duplex formation, Endogenous, Gene expression, High levels, Human immunodeficiency virus type, Hybrid, Intramolecular interactions, Mrna, Natural antisense rnas, Nucleic acids, Pacl, Personal communication, Rna, Selectivity.
Abstract
Abstract: The transient or permanent expression of antisense RNA represents one option to apply antisense techniques in biotechnology and medical research. Despite the increasing importance and use of antisense nucleic acids as well as their significant antisense-specific phenotypic effects in vivo, there is an obvious lack of explanation for the mechanism of their action. By studying naturally occurring antisense RNA and analyzing their mechanism of action we attempt to learn more about the design, the use, and the critical parameters of artificial antisense RNA. Attempts to derive models from biochemical and structural studies for the interactions between antisense RNAs and their targets will be discussed.
Url:
DOI: 10.1007/BF02762319
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<affiliation wicri:level="1"><mods:affiliation>Dept. of Genetics, Univ. Kassel, Heinrich-Plett-Str. 40, 34109, Kassel, Germany</mods:affiliation>
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<keywords scheme="Teeft" xml:lang="en"><term>Annealing</term>
<term>Antisense</term>
<term>Antisense machinery</term>
<term>Antisense mechanisms</term>
<term>Antisense rnas</term>
<term>Antisense transcripts</term>
<term>Artificial antisense</term>
<term>Biol</term>
<term>Cellular proteins</term>
<term>Complementary sequences</term>
<term>Complementary strands</term>
<term>Degradation</term>
<term>Dictyostelium</term>
<term>Dsrna</term>
<term>Duplex</term>
<term>Duplex formation</term>
<term>Endogenous</term>
<term>Gene expression</term>
<term>High levels</term>
<term>Human immunodeficiency virus type</term>
<term>Hybrid</term>
<term>Intramolecular interactions</term>
<term>Mrna</term>
<term>Natural antisense rnas</term>
<term>Nucleic acids</term>
<term>Pacl</term>
<term>Personal communication</term>
<term>Rna</term>
<term>Selectivity</term>
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<front><div type="abstract" xml:lang="en">Abstract: The transient or permanent expression of antisense RNA represents one option to apply antisense techniques in biotechnology and medical research. Despite the increasing importance and use of antisense nucleic acids as well as their significant antisense-specific phenotypic effects in vivo, there is an obvious lack of explanation for the mechanism of their action. By studying naturally occurring antisense RNA and analyzing their mechanism of action we attempt to learn more about the design, the use, and the critical parameters of artificial antisense RNA. Attempts to derive models from biochemical and structural studies for the interactions between antisense RNAs and their targets will be discussed.</div>
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