mtRF1a is a human mitochondrial translation release factor decoding the major termination Codons UAA and UAG

被引:104
|
作者
Soleimanpour-Lichaei, Hamid Reza
Khul, Inge
Gaisne, Mauricette
Passos, Joao F.
Wydro, Mlateusz
Rorbach, Joanna
Temperley, Richard
Bonnefoy, Nathalie
Tate, Warren
Lightowlers, Robert
Chrzanowska-Lightowlers, Zofia
机构
[1] Univ Newcastle Upon Tyne, Mitochondrial Res Grp, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
[2] CNRS, Ctr Genet Mol, F-91198 Gif Sur Yvette, France
[3] Univ Otago, Dept Biochem, Dunedin 9016, New Zealand
[4] Univ Newcastle Upon Tyne, Ctr Integrated Syst Biol Ageing & Nutr, Newcastle Upon Tyne NE4 6BE, Tyne & Wear, England
基金
英国惠康基金;
关键词
D O I
10.1016/j.molcel.2007.06.031
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
Human mitochondria contain their own genome, encoding 13 polypeptides that are synthesized within the organelle. The molecular processes that govern and facilitate this mitochondrial translation remain unclear. Many key factors have yet to be characterized-for example, those required for translation termination. All other systems have two classes of release factors that either promote codon-specific hydrolysis of peptidyl-tRNA (class 1) or lack specificity but stimulate the dissociation of class I factors from the ribosome (class 11). One human mitochondrial protein has been previously identified in silico as a putative member of the class I release factors. Although we could not confirm the function of this factor, we report the identification of a different mitochondrial protein, mtRF1 a, that is capable in vitro and in vivo of terminating translation at UAA/UAG codons. Further, mtRF1a depletion in HeLa cells led to compromised growth in galactose and increased production of reactive oxygen species.
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页码:745 / 757
页数:13
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