Chomyn A, Cleeter M W, Ragan C I, Riley M, Doolittle R F, Attardi G
Science. 1986 Oct 31;234(4776):614-8. doi: 10.1126/science.3764430.
The polypeptide encoded in URF6, the last unassigned reading frame of human mitochondrial DNA, has been identified with antibodies to peptides predicted from the DNA sequence. Antibodies prepared against highly purified respiratory chain NADH dehydrogenase from beef heart or against the cytoplasmically synthesized 49-kilodalton iron-sulfur subunit isolated from this enzyme complex, when added to a deoxycholate or a Triton X-100 mitochondrial lysate of HeLa cells, specifically precipitated the URF6 product together with the six other URF products previously identified as subunits of NADH dehydrogenase. These results strongly point to the URF6 product as being another subunit of this enzyme complex. Thus, almost 60% of the protein coding capacity of mammalian mitochondrial DNA is utilized for the assembly of the first enzyme complex of the respiratory chain. The absence of such information in yeast mitochondrial DNA dramatizes the variability in gene content of different mitochondrial genomes.
人类线粒体DNA最后一个未确定的阅读框URF6中编码的多肽,已通过针对从DNA序列预测的肽段制备的抗体得以鉴定。用针对牛肉心高度纯化的呼吸链NADH脱氢酶或针对从该酶复合物中分离出的细胞质合成的49千道尔顿铁硫亚基制备的抗体,添加到HeLa细胞的脱氧胆酸盐或Triton X - 100线粒体裂解物中时,会特异性沉淀出URF6产物以及先前鉴定为NADH脱氢酶亚基的其他六种URF产物。这些结果有力地表明URF6产物是该酶复合物的另一个亚基。因此,哺乳动物线粒体DNA几乎60%的蛋白质编码能力用于呼吸链第一个酶复合物的组装。酵母线粒体DNA中缺乏此类信息凸显了不同线粒体基因组基因含量的变异性。