Allison D S, Schatz G
Proc Natl Acad Sci U S A. 1986 Dec;83(23):9011-5. doi: 10.1073/pnas.83.23.9011.
Synthetic oligonucleotides were used to construct artificial mitochondrial presequences that contained, besides the initiator methionine, only arginine, serine, and leucine. The ratio of these three amino acids was adjusted to match that of basic, hydroxylated, and hydrophobic residues in natural mitochondrial presequences. When these sequences were fused to the N terminus of yeast cytochrome oxidase subunit IV lacking its own presequence, they directed the attached subunit IV to its correct intramitochondrial location in vivo. They also mediated import of subunit IV into isolated yeast mitochondria. In contrast, artificial sequences containing glutamine, arginine, and serine residues following the initiator methionine were inactive. Thus, the targeting function of mitochondrial presequences does not depend on specific amino acid sequences but may instead depend on the overall balance between basic, hydrophobic, and hydroxylated amino acids.
合成寡核苷酸被用于构建人工线粒体前导序列,这些序列除了起始甲硫氨酸外,仅包含精氨酸、丝氨酸和亮氨酸。调整这三种氨基酸的比例,以使其与天然线粒体前导序列中的碱性、羟基化和疏水残基的比例相匹配。当这些序列与缺乏自身前导序列的酵母细胞色素氧化酶亚基IV的N末端融合时,它们在体内将附着的亚基IV引导至其正确的线粒体内位置。它们还介导亚基IV导入分离的酵母线粒体。相比之下,在起始甲硫氨酸之后包含谷氨酰胺、精氨酸和丝氨酸残基的人工序列没有活性。因此,线粒体前导序列的靶向功能不依赖于特定的氨基酸序列,而是可能依赖于碱性、疏水和羟基化氨基酸之间的整体平衡。