Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
Cell Metab. 2011 May 4;13(5):527-39. doi: 10.1016/j.cmet.2011.04.002.
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.
精确控制线粒体 DNA 基因表达对于哺乳动物氧化磷酸化能力的调节至关重要。MTERF 蛋白家族在这个过程中起着关键作用,其成员被牵连到转录起始和特异性转录终止的调节中。我们现在证明,该家族的一个成员 MTERF4 直接控制着线粒体核糖体的生物发生和翻译。MTERF4 与核糖体 RNA 甲基转移酶 NSUN4 形成化学计量复合物,并需要该因子募集到大核糖体亚基。MTERF4 的缺失导致核糖体组装缺陷和翻译的急剧减少。因此,我们的结果表明 MTERF4 是哺乳动物线粒体翻译的重要调节剂。