Literature DB >> 12815338

Nucleic acid-based techniques for post-transcriptional regulation of molecular targets.

George Jarad1, Jeffrey S Simske, John R Sedor, Jeffrey R Schelling.   

Abstract

PURPOSE OF REVIEW: Messenger RNA, transfer RNA and ribosomal RNA were defined long ago as essential components for transmission of genetic code from DNA. However, there are many other, less commonly recognized RNAs, such as ribozymes and small interfering RNAs, which are distinguished by their ability to inhibit RNA function. This review describes the basic molecular concepts and potential therapeutic applications of RNA inhibition by a variety of molecules, including ribozymes, antisense oligonucleotides, aptamers and small interfering RNAs. RECENT
FINDINGS: A tremendous amount of data has recently emerged about double-stranded small interfering RNAs, which bind and degrade corresponding messenger RNAs by a process called RNA interference. Though native small interfering RNAs have been shown to be biologically relevant in animals and plants, synthetic types have rapidly become powerful tools for post-transcriptional inhibition of specific gene products to determine functional consequences in simple organisms and in-vitro model systems. More established means of RNA inhibition, such as with ribozyme and antisense strategies, continue to be viable options for in-vitro experiments, and form the basis for many ongoing clinical trials.
SUMMARY: Ribozymes, antisense oligonucleotides, aptamers and small interfering RNAs are potentially useful reagents for in-vitro investigation and for treatment of kidney and hypertension diseases.

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Year:  2003        PMID: 12815338     DOI: 10.1097/00041552-200307000-00010

Source DB:  PubMed          Journal:  Curr Opin Nephrol Hypertens        ISSN: 1062-4821            Impact factor:   2.894


  1 in total

1.  Topical delivery of anti-sense oligonucleotides using low-frequency sonophoresis.

Authors:  Ahmet Tezel; Sujatha Dokka; Susan Kelly; Gregory E Hardee; Samir Mitragotri
Journal:  Pharm Res       Date:  2004-12       Impact factor: 4.200

  1 in total

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