Antisense technologies

Improvement through novel chemical modifications

Authors

Errata

This article is corrected by:

  1. Errata: Corrigendum Volume 274, Issue 8, 2161, Article first published online: 27 March 2007

J. Kurreck, Institut für Chemie-Biochemie, Freie Universität Berlin, Thielallee 63, 14195 Berlin, Germany. Fax: + 49 30 83 85 64 13, Tel.: + 49 30 83 85 69 69, E-mail: jkurreck@chemie.fu-berlin.de

Abstract

Antisense agents are valuable tools to inhibit the expression of a target gene in a sequence-specific manner, and may be used for functional genomics, target validation and therapeutic purposes. Three types of anti-mRNA strategies can be distinguished. Firstly, the use of single stranded antisense-oligonucleotides; secondly, the triggering of RNA cleavage through catalytically active oligonucleotides referred to as ribozymes; and thirdly, RNA interference induced by small interfering RNA molecules. Despite the seemingly simple idea to reduce translation by oligonucleotides complementary to an mRNA, several problems have to be overcome for successful application. Accessible sites of the target RNA for oligonucleotide binding have to be identified, antisense agents have to be protected against nucleolytic attack, and their cellular uptake and correct intracellular localization have to be achieved. Major disadvantages of commonly used phosphorothioate DNA oligonucleotides are their low affinity towards target RNA molecules and their toxic side-effects. Some of these problems have been solved in ‘second generation’ nucleotides with alkyl modifications at the 2′ position of the ribose. In recent years valuable progress has been achieved through the development of novel chemically modified nucleotides with improved properties such as enhanced serum stability, higher target affinity and low toxicity. In addition, RNA-cleaving ribozymes and deoxyribozymes, and the use of 21-mer double-stranded RNA molecules for RNA interference applications in mammalian cells offer highly efficient strategies to suppress the expression of a specific gene.

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