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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...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2006
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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. |
format | Text |
id | pubmed-1557819 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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