Medical Journals

Mterf3 is a Negative Regulator of Mammalian Mtdna Transcription.

Authors:
  • Park Chan Bae
  • Asin-Cayuela Jorge
  • Cámara Yolanda
  • Shi Yonghong
  • Pellegrini Mina
  • Gaspari Martina
  • Wibom Rolf
  • Hultenby Kjell
  • Erdjument-Bromage Hediye
  • Tempst Paul
  • Falkenberg Maria
  • Gustafsson Claes M
  • Larsson Nils-Göran

From: Department of Laboratory Medicine, Karolinska Institutet, S-141 86 Stockholm, Sweden.

Cell

  • Publish Date: Jul 2007
  • ISSN: 0092-8674
  • Volume: 130
  • Issue: 2
  • Pages: 273-85
  • Medium: Print
  • Language: English
  • Citation (JAMA): Park Chan Bae, Asin-Cayuela Jorge, Cámara Yolanda, et al. Mterf3 is a Negative Regulator of Mammalian Mtdna Transcription.. Cell Jul 2007;130:273-85

Abstract

Regulation of mammalian mtDNA gene expression is critical for altering oxidative phosphorylation capacity in response to physiological demands and disease processes. The basal machinery for initiation of mtDNA transcription has been molecularly defined, but the mechanisms regulating its activity are poorly understood. In this study, we show that MTERF3 is a negative regulator of mtDNA transcription initiation. The MTERF3 gene is essential because homozygous knockout mouse embryos die in midgestation. Tissue-specific inactivation of MTERF3 in the heart causes aberrant mtDNA transcription and severe respiratory chain deficiency. MTERF3 binds the mtDNA promoter region and depletion of MTERF3 increases transcription initiation on both mtDNA strands. This increased transcription initiation leads to decreased expression of critical promoter-distal tRNA genes, which is possibly explained by transcriptional collision on the circular mtDNA molecule. To our knowledge, MTERF3 is the first example of a mitochondrial protein that acts as a specific repressor of mammalian mtDNA transcription initiation in vivo.

Mesh Headings (Keywords): Animals, DNA, Mitochondrial, Down-Regulation, Electron Transport, Embryo, Mammalian, Embryonic Development, Gene Targeting, Genes, Essential, Hela Cells, Humans, Mice, Mice, Knockout, Mitochondria, Mitochondrial Proteins, Myocardium, Organ Specificity, Phenotype, Promoter Regions (Genetics), Protein Binding, RNA, Messenger, Transcription Factors, Transcription, Genetic


Check for Full Text / PubMed Unique Identifier (PMID): 17662942


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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