A delayed-early response nuclear gene encoding MRPL12, the mitochondrial homologue to the bacterial translational regulator L7/L12 protein

被引:32
作者
Marty, L
Fort, P
机构
[1] UNIV MONTPELLIER 1,CNRS,INST MOLEC GENET,UMR5535,F-34033 MONTPELLIER,FRANCE
[2] UNIV MONTPELLIER 2,CNRS,INST MOLEC GENET,F-34033 MONTPELLIER,FRANCE
关键词
D O I
10.1074/jbc.271.19.11468
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have characterized a new delayed-early response mRNA encoding a 21-kDa product (MRPL12) that accumulates during the G(1) phase of growth-stimulated cells. MRPL12 is the mammalian homologue to chloroplastic and bacterial L12 ribosomal proteins. Immunofluorescence microscopy and cell fractionation indicate a predominant mitochondrial localization in various mammalian cell lines. The NH2-terminal 49 amino acids are necessary and sufficient to target the protein within the mitochondria and are probably cleaved off during import. MRPL12 proteins associate in vitro and cofractionate with ribosomal structures, as is the case for prokaryotic L12 proteins. Expression of a dominant inhibitory truncated protein leads to a severe reduction in cell growth by inhibiting mitochondrial ATP production. MRPL12 is the first mammalian mitochondrial ribosomal protein to be characterized.
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页码:11468 / 11476
页数:9
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