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Synthetic polyamines stimulate in vitro transcription by T7 RNA polymerase

Identifieur interne : 004311 ( Main/Exploration ); précédent : 004310; suivant : 004312

Synthetic polyamines stimulate in vitro transcription by T7 RNA polymerase

Auteurs : Magali Frugier [France] ; Catherine Florentz [France] ; Mir Wais Hosseini [France] ; Jean-Marie Lehn [France] ; Richard Giegé [France]

Source :

RBID : ISTEX:3257ECF5F1C7E888BB790311B53D71B9AAD8EF97

Descripteurs français

English descriptors

Abstract

The influence of nine synthetic polyamines on in vitro transcription with T7 RNA polymerase has been studied. The compounds used were linear or macrocyclic tetra- and hexaamine, varying in their size, shape and number of protonated groups. Their effect was tested on different types of templates, all presenting the T7 RNA promoter in a double-stranded form followed by sequences encoding short transcripts 25 to 35-mers) either on single- or double-stranded synthetic oligodeoxyribonucleotides. All polyamines used stimulate transcription of both types of templates at levels dependent on their size, shape, protonation degree, and concentration. For each compound, an optimal concentration could be defined; above this concentration, transcription inhibition occurred. Highest stimulation (up to 12-fold) was obtained by the largest cyclic compound called [38JN6C10.

Url:
DOI: 10.1093/nar/22.14.2784


Affiliations:


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Le document en format XML

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<term>DNA-Directed RNA Polymerases (metabolism)</term>
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<front>
<div type="abstract">The influence of nine synthetic polyamines on in vitro transcription with T7 RNA polymerase has been studied. The compounds used were linear or macrocyclic tetra- and hexaamine, varying in their size, shape and number of protonated groups. Their effect was tested on different types of templates, all presenting the T7 RNA promoter in a double-stranded form followed by sequences encoding short transcripts 25 to 35-mers) either on single- or double-stranded synthetic oligodeoxyribonucleotides. All polyamines used stimulate transcription of both types of templates at levels dependent on their size, shape, protonation degree, and concentration. For each compound, an optimal concentration could be defined; above this concentration, transcription inhibition occurred. Highest stimulation (up to 12-fold) was obtained by the largest cyclic compound called [38JN6C10.</div>
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