Towpik Joanna, Chaciñska Agnieszka, Ciesla Malgorzata, Ginalski Krzysztof, Boguta Magdalena
Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Pawiñskiego 5A, 02-106 Warsaw, Poland.
J Biol Chem. 2004 Apr 2;279(14):14096-103. doi: 10.1074/jbc.M312856200. Epub 2004 Jan 19.
Although the control of mitochondrial translation in the yeast Saccharomyces cerevisiae has been studied extensively, the mechanism of termination remains obscure. Ten mutations isolated in a genetic screen for read-through of premature stop codons in mitochondrial genes were localized in the chromosomal gene encoding the mitochondrial release factor mRF1. The mrf1-13 and mrf1-780 mutant genes, in contrast to other alleles, caused a non-respiratory phenotype that correlated with decreased expression of mitochondrial genes as well as a reporter ARG8(m) gene inserted into mitochondrial DNA. The steady-state levels of several mitochondrially encoded proteins, but not their mRNAs, were dramatically decreased in mrf1-13 and mrf1-780 cells. Structural models of mRF1 were constructed, allowing localization of residues substituted in the mrf1 mutants and offering an insight into the possible mechanism by which these mutations change the mitochondrial translation termination fidelity. Inhibition of mitochondrial translation in mrf1-13 and mrf1-780 correlated with the three-dimensional localization of the mutated residues close to the PST motif presumably involved in the recognition of stop codons in mitochondrial mRNA.
尽管对酿酒酵母中线粒体翻译的控制已进行了广泛研究,但终止机制仍不清楚。在一项针对线粒体基因中过早终止密码子通读的遗传筛选中分离出的10个突变,定位在编码线粒体释放因子mRF1的染色体基因中。与其他等位基因不同,mrf1-13和mrf1-780突变基因导致了一种非呼吸表型,这与线粒体基因以及插入线粒体DNA的报告基因ARG8(m)的表达降低相关。在mrf1-13和mrf1-780细胞中,几种线粒体编码蛋白的稳态水平显著降低,但其mRNA水平未降低。构建了mRF1的结构模型,从而确定了mrf1突变体中被取代的残基位置,并深入了解了这些突变改变线粒体翻译终止保真度的可能机制。mrf1-13和mrf1-780中线粒体翻译的抑制与靠近PST基序的突变残基的三维定位相关,该基序可能参与线粒体mRNA中终止密码子的识别。