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Elongation complexes of Thermus thermophilus RNA polymerase that possess distinct translocation conformations

We have characterized elongation complexes (ECs) of RNA polymerase from the extremely thermophilic bacterium, Thermus thermophilus. We found that complexes assembled on nucleic acid scaffolds are transcriptionally competent at high temperature (50–80°C) and, depending upon the organization of the sc...

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Autores principales: Kashkina, Ekaterina, Anikin, Michael, Tahirov, Tahir H., Kochetkov, Sergei N., Vassylyev, Dmitry G., Temiakov, Dmitry
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1557819/
https://www.ncbi.nlm.nih.gov/pubmed/16914440
http://dx.doi.org/10.1093/nar/gkl559
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author Kashkina, Ekaterina
Anikin, Michael
Tahirov, Tahir H.
Kochetkov, Sergei N.
Vassylyev, Dmitry G.
Temiakov, Dmitry
author_facet Kashkina, Ekaterina
Anikin, Michael
Tahirov, Tahir H.
Kochetkov, Sergei N.
Vassylyev, Dmitry G.
Temiakov, Dmitry
author_sort Kashkina, Ekaterina
collection PubMed
description We have characterized elongation complexes (ECs) of RNA polymerase from the extremely thermophilic bacterium, Thermus thermophilus. We found that complexes assembled on nucleic acid scaffolds are transcriptionally competent at high temperature (50–80°C) and, depending upon the organization of the scaffold, possess distinct translocation conformations. ECs assembled on scaffolds with a 9 bp RNA:DNA hybrid are highly stable, resistant to pyrophosphorolysis, and are in the posttranslocated state. ECs with an RNA:DNA hybrid longer or shorter than 9 bp appear to be in a pretranslocated state, as evidenced by their sensitivity to pyrophosphorolysis, GreA-induced cleavage, and exonuclease footprinting. Both pretranslocated (8 bp RNA:DNA hybrid) and posttranslocated (9 bp RNA:DNA hybrid) complexes were crystallized in distinct crystal forms, supporting the homogeneity of the conformational states in these complexes. Crystals of a posttranslocated complex were used to collect diffraction data at atomic resolution.
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spelling pubmed-15578192006-09-06 Elongation complexes of Thermus thermophilus RNA polymerase that possess distinct translocation conformations Kashkina, Ekaterina Anikin, Michael Tahirov, Tahir H. Kochetkov, Sergei N. Vassylyev, Dmitry G. Temiakov, Dmitry Nucleic Acids Res Nucleic Acid Enzymes We have characterized elongation complexes (ECs) of RNA polymerase from the extremely thermophilic bacterium, Thermus thermophilus. We found that complexes assembled on nucleic acid scaffolds are transcriptionally competent at high temperature (50–80°C) and, depending upon the organization of the scaffold, possess distinct translocation conformations. ECs assembled on scaffolds with a 9 bp RNA:DNA hybrid are highly stable, resistant to pyrophosphorolysis, and are in the posttranslocated state. ECs with an RNA:DNA hybrid longer or shorter than 9 bp appear to be in a pretranslocated state, as evidenced by their sensitivity to pyrophosphorolysis, GreA-induced cleavage, and exonuclease footprinting. Both pretranslocated (8 bp RNA:DNA hybrid) and posttranslocated (9 bp RNA:DNA hybrid) complexes were crystallized in distinct crystal forms, supporting the homogeneity of the conformational states in these complexes. Crystals of a posttranslocated complex were used to collect diffraction data at atomic resolution. Oxford University Press 2006 2006-08-16 /pmc/articles/PMC1557819/ /pubmed/16914440 http://dx.doi.org/10.1093/nar/gkl559 Text en © 2006 The Author(s).
spellingShingle Nucleic Acid Enzymes
Kashkina, Ekaterina
Anikin, Michael
Tahirov, Tahir H.
Kochetkov, Sergei N.
Vassylyev, Dmitry G.
Temiakov, Dmitry
Elongation complexes of Thermus thermophilus RNA polymerase that possess distinct translocation conformations
title Elongation complexes of Thermus thermophilus RNA polymerase that possess distinct translocation conformations
title_full Elongation complexes of Thermus thermophilus RNA polymerase that possess distinct translocation conformations
title_fullStr Elongation complexes of Thermus thermophilus RNA polymerase that possess distinct translocation conformations
title_full_unstemmed Elongation complexes of Thermus thermophilus RNA polymerase that possess distinct translocation conformations
title_short Elongation complexes of Thermus thermophilus RNA polymerase that possess distinct translocation conformations
title_sort elongation complexes of thermus thermophilus rna polymerase that possess distinct translocation conformations
topic Nucleic Acid Enzymes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1557819/
https://www.ncbi.nlm.nih.gov/pubmed/16914440
http://dx.doi.org/10.1093/nar/gkl559
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