| Literature DB >> 23562081 |
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.Entities:
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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