Literature DB >> 23562081

MTERF1 binds mtDNA to prevent transcriptional interference at the light-strand promoter but is dispensable for rRNA gene transcription regulation.

Mügen Terzioglu1, Benedetta Ruzzenente, Julia Harmel, Arnaud Mourier, Elisabeth Jemt, Marcela Dávila López, Christian Kukat, James B Stewart, Rolf Wibom, Caroline Meharg, Bianca Habermann, Maria Falkenberg, Claes M Gustafsson, Chan Bae Park, Nils-Göran Larsson.   

Abstract

Mitochondrial transcription termination factor 1, MTERF1, has been reported to couple rRNA gene transcription initiation with termination and is therefore thought to be a key regulator of mammalian mitochondrial ribosome biogenesis. The prevailing model is based on a series of observations published over the last two decades, but no in vivo evidence exists to show that MTERF1 regulates transcription of the heavy-strand region of mtDNA containing the rRNA genes. Here, we demonstrate that knockout of Mterf1 in mice has no effect on mitochondrial rRNA levels or mitochondrial translation. Instead, loss of Mterf1 influences transcription initiation at the light-strand promoter, resulting in a decrease of de novo transcription manifested as reduced 7S RNA levels. Based on these observations, we suggest that MTERF1 does not regulate heavy-strand transcription, but rather acts to block transcription on the opposite strand of mtDNA to prevent transcription interference at the light-strand promoter.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23562081     DOI: 10.1016/j.cmet.2013.03.006

Source DB:  PubMed          Journal:  Cell Metab        ISSN: 1550-4131            Impact factor:   27.287


  44 in total

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Review 3.  Structural basis of mitochondrial transcription.

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5.  mTERF8, a Member of the Mitochondrial Transcription Termination Factor Family, Is Involved in the Transcription Termination of Chloroplast Gene psbJ.

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Review 10.  The dynamics of mitochondrial DNA heteroplasmy: implications for human health and disease.

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