| Literature DB >> 21531335 |
Yolanda Cámara1, Jorge Asin-Cayuela, Chan Bae Park, Metodi D Metodiev, Yonghong Shi, Benedetta Ruzzenente, Christian Kukat, Bianca Habermann, Rolf Wibom, Kjell Hultenby, Thomas Franz, Hediye Erdjument-Bromage, Paul Tempst, B Martin Hallberg, Claes M Gustafsson, Nils-Göran Larsson.
Abstract
Precise control of mitochondrial DNA gene expression is critical for regulation of oxidative phosphorylation capacity in mammals. The MTERF protein family plays a key role in this process, and its members have been implicated in regulation of transcription initiation and site-specific transcription termination. We now demonstrate that a member of this family, MTERF4, directly controls mitochondrial ribosomal biogenesis and translation. MTERF4 forms a stoichiometric complex with the ribosomal RNA methyltransferase NSUN4 and is necessary for recruitment of this factor to the large ribosomal subunit. Loss of MTERF4 leads to defective ribosomal assembly and a drastic reduction in translation. Our results thus show that MTERF4 is an important regulator of translation in mammalian mitochondria.Entities:
Mesh:
Substances:
Year: 2011 PMID: 21531335 DOI: 10.1016/j.cmet.2011.04.002
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287