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Role of the RNA/DNA kinase Grc3 in transcription termination by RNA polymerase I

Transcription termination by RNA polymerase I in Saccharomyces cerevisiae is mediated by a ‘torpedo' mechanism: co-transcriptional RNA cleavage by Rnt1 at the ribosomal DNA 3′-region generates a 5′-end that is recognized by the 5′–3′ exonuclease Rat1; this degrades the downstream transcript and...

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Autores principales: Braglia, Priscilla, Heindl, Katrin, Schleiffer, Alexander, Martinez, Javier, Proudfoot, Nick J
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2948184/
https://www.ncbi.nlm.nih.gov/pubmed/20814424
http://dx.doi.org/10.1038/embor.2010.130
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author Braglia, Priscilla
Heindl, Katrin
Schleiffer, Alexander
Martinez, Javier
Proudfoot, Nick J
author_facet Braglia, Priscilla
Heindl, Katrin
Schleiffer, Alexander
Martinez, Javier
Proudfoot, Nick J
author_sort Braglia, Priscilla
collection PubMed
description Transcription termination by RNA polymerase I in Saccharomyces cerevisiae is mediated by a ‘torpedo' mechanism: co-transcriptional RNA cleavage by Rnt1 at the ribosomal DNA 3′-region generates a 5′-end that is recognized by the 5′–3′ exonuclease Rat1; this degrades the downstream transcript and eventually causes termination. In this study, we identify Grc3 as a new factor involved in this process. We demonstrate that GRC3, an essential gene of previously unknown function, encodes a polynucleotide kinase that is required for efficient termination by RNA polymerase I. We propose that it controls the phosphorylation status of the downstream Rnt1 cleavage product and thereby regulates its accessibility to the torpedo Rat1.
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spelling pubmed-29481842010-10-25 Role of the RNA/DNA kinase Grc3 in transcription termination by RNA polymerase I Braglia, Priscilla Heindl, Katrin Schleiffer, Alexander Martinez, Javier Proudfoot, Nick J EMBO Rep Scientific Reports Transcription termination by RNA polymerase I in Saccharomyces cerevisiae is mediated by a ‘torpedo' mechanism: co-transcriptional RNA cleavage by Rnt1 at the ribosomal DNA 3′-region generates a 5′-end that is recognized by the 5′–3′ exonuclease Rat1; this degrades the downstream transcript and eventually causes termination. In this study, we identify Grc3 as a new factor involved in this process. We demonstrate that GRC3, an essential gene of previously unknown function, encodes a polynucleotide kinase that is required for efficient termination by RNA polymerase I. We propose that it controls the phosphorylation status of the downstream Rnt1 cleavage product and thereby regulates its accessibility to the torpedo Rat1. Nature Publishing Group 2010-10 2010-09-03 /pmc/articles/PMC2948184/ /pubmed/20814424 http://dx.doi.org/10.1038/embor.2010.130 Text en Copyright © 2010, European Molecular Biology Organization http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial No Derivative Works 3.0 Unported License, which permits distribution and reproduction in any medium, provided the original author and source are credited. This license does not permit commercial exploitation or the creation of derivative works without specific permission.
spellingShingle Scientific Reports
Braglia, Priscilla
Heindl, Katrin
Schleiffer, Alexander
Martinez, Javier
Proudfoot, Nick J
Role of the RNA/DNA kinase Grc3 in transcription termination by RNA polymerase I
title Role of the RNA/DNA kinase Grc3 in transcription termination by RNA polymerase I
title_full Role of the RNA/DNA kinase Grc3 in transcription termination by RNA polymerase I
title_fullStr Role of the RNA/DNA kinase Grc3 in transcription termination by RNA polymerase I
title_full_unstemmed Role of the RNA/DNA kinase Grc3 in transcription termination by RNA polymerase I
title_short Role of the RNA/DNA kinase Grc3 in transcription termination by RNA polymerase I
title_sort role of the rna/dna kinase grc3 in transcription termination by rna polymerase i
topic Scientific Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2948184/
https://www.ncbi.nlm.nih.gov/pubmed/20814424
http://dx.doi.org/10.1038/embor.2010.130
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