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The proteomes of transcription factories containing RNA polymerases I, II or III

Human nuclei contain three RNA polymerases (I, II, and III) that transcribe different groups of genes; the active forms of all three are difficult to isolate because they are bound to the substructure. Here, we describe a purification approach for isolating active RNA polymerase complexes from mamma...

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Detalles Bibliográficos
Autores principales: Melnik, Svitlana, Deng, Binwei, Papantonis, Argyris, Baboo, Sabyasachi, Carr, Ian M., Cook, Peter R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3324775/
https://www.ncbi.nlm.nih.gov/pubmed/21946667
http://dx.doi.org/10.1038/nmeth.1705
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author Melnik, Svitlana
Deng, Binwei
Papantonis, Argyris
Baboo, Sabyasachi
Carr, Ian M.
Cook, Peter R
author_facet Melnik, Svitlana
Deng, Binwei
Papantonis, Argyris
Baboo, Sabyasachi
Carr, Ian M.
Cook, Peter R
author_sort Melnik, Svitlana
collection PubMed
description Human nuclei contain three RNA polymerases (I, II, and III) that transcribe different groups of genes; the active forms of all three are difficult to isolate because they are bound to the substructure. Here, we describe a purification approach for isolating active RNA polymerase complexes from mammalian cells. After isolation, we analyzed their protein content by mass spectrometry. Each complex represents part of the core of a transcription factory; for example, the RNA polymerase II complex contains subunits unique to RNA polymerase II plus various transcription factors, but shares a number of ribonucleoproteins with the other polymerase complexes; it is also rich in polymerase II transcripts. We also describe a native chromosome conformation capture method to confirm that the complexes remain attached to the same pairs of DNA templates found in vivo.
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spelling pubmed-33247752012-05-01 The proteomes of transcription factories containing RNA polymerases I, II or III Melnik, Svitlana Deng, Binwei Papantonis, Argyris Baboo, Sabyasachi Carr, Ian M. Cook, Peter R Nat Methods Article Human nuclei contain three RNA polymerases (I, II, and III) that transcribe different groups of genes; the active forms of all three are difficult to isolate because they are bound to the substructure. Here, we describe a purification approach for isolating active RNA polymerase complexes from mammalian cells. After isolation, we analyzed their protein content by mass spectrometry. Each complex represents part of the core of a transcription factory; for example, the RNA polymerase II complex contains subunits unique to RNA polymerase II plus various transcription factors, but shares a number of ribonucleoproteins with the other polymerase complexes; it is also rich in polymerase II transcripts. We also describe a native chromosome conformation capture method to confirm that the complexes remain attached to the same pairs of DNA templates found in vivo. 2011-09-25 /pmc/articles/PMC3324775/ /pubmed/21946667 http://dx.doi.org/10.1038/nmeth.1705 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Melnik, Svitlana
Deng, Binwei
Papantonis, Argyris
Baboo, Sabyasachi
Carr, Ian M.
Cook, Peter R
The proteomes of transcription factories containing RNA polymerases I, II or III
title The proteomes of transcription factories containing RNA polymerases I, II or III
title_full The proteomes of transcription factories containing RNA polymerases I, II or III
title_fullStr The proteomes of transcription factories containing RNA polymerases I, II or III
title_full_unstemmed The proteomes of transcription factories containing RNA polymerases I, II or III
title_short The proteomes of transcription factories containing RNA polymerases I, II or III
title_sort proteomes of transcription factories containing rna polymerases i, ii or iii
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3324775/
https://www.ncbi.nlm.nih.gov/pubmed/21946667
http://dx.doi.org/10.1038/nmeth.1705
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