Weiss-Brummer B, Sakai H, Hüttenhofer A
Institut für Genetik und Mikrobiologie, Universität München, Federal Republic of Germany.
Curr Genet. 1989 Apr;15(4):239-46. doi: 10.1007/BF00447038.
A polypeptide chain-terminating mutation (M5631) previously has been shown to be a +1T insertion in the yeast mitochondrial gene oxi1, coding for subunit II of the cytochrome c oxidase. A spontaneously arisen frameshift suppressor (mfs-1) that is mitochondrially inherited suppresses this mutation to a considerable extent. The suppressor mutation was mapped by genetic and molecular analyses in the mitochondrial tRNASer-var1 region of the mitochondrial genome of the yeast S. cerevisiae. Genetic analyses show that the suppressor mfs-1 does not suppress other known mitochondrial frameshift mutations, or missense and nonsense mutations.
先前已表明,一种多肽链终止突变(M5631)是酵母线粒体基因oxi1中的一个+1T插入突变,该基因编码细胞色素c氧化酶的亚基II。一种线粒体遗传的自发产生的移码抑制子(mfs-1)在很大程度上抑制了这种突变。通过遗传和分子分析,将该抑制子突变定位在酿酒酵母线粒体基因组的线粒体tRNASer-var1区域。遗传分析表明,抑制子mfs-1不抑制其他已知的线粒体移码突变、错义突变和无义突变。