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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.

Original publication

DOI

10.1038/embor.2010.130

Type

Journal article

Journal

EMBO Rep

Publication Date

10/2010

Volume

11

Pages

758 - 764

Keywords

DNA Polymerase I, DNA, Ribosomal, Phosphorylation, Polynucleotide 5'-Hydroxyl-Kinase, RNA Polymerase I, RNA Processing, Post-Transcriptional, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins, Terminator Regions, Genetic, Transcription, Genetic