Lundin M, Baltscheffsky H, Ronne H
Department of Biochemistry, Arrhenius Laboratories for Natural Sciences, University of Stockholm, Sweden.
J Biol Chem. 1991 Jul 5;266(19):12168-72.
We have cloned a gene encoding a mitochondrial inorganic pyrophosphatase (PPase) in the yeast Saccharomyces cerevisiae by low stringency hybridization to PPA1, the yeast gene for cytoplasmic PPase. The new gene, PPA2, is located on chromosome 13 and encodes a protein whose sequence is 49% identical to the cytoplasmic enzyme. The protein differs from cytoplasmic PPase in that it has a leader sequence enriched in basic and hydroxylated residues, which is typically found in mitochondrial proteins. Yeast cells overproducing PPA2 had a 47-fold increase in mitochondrial PPase activity. This activity was further stimulated 3-fold by the uncoupler carbonyl cyanide p-trifluoromethoxyphenylhydrazone, which suggests that PPA2 is part of an energy-linked enzyme. Using gene disruptions, we found that PPA1 is required for cell growth. In contrast, cells disrupted for PPA2 are viable, but unable to grow on respiratory carbon sources. Fluorescence microscopy revealed that these cells have lost their mitochondrial DNA. We conclude that the mitochondrial PPase encoded by PPA2 is essential for mitochondrial function and maintenance of the mitochondrial genome.
我们通过与酵母细胞质无机焦磷酸酶(PPase)的基因PPA1进行低严谨度杂交,克隆了酿酒酵母中一个编码线粒体无机焦磷酸酶(PPase)的基因。新基因PPA2位于13号染色体上,编码一种与细胞质酶序列有49%同一性的蛋白质。该蛋白质与细胞质PPase的不同之处在于它有一个富含碱性和羟基化残基的前导序列,这在典型的线粒体蛋白质中常见。过量表达PPA2的酵母细胞线粒体PPase活性增加了47倍。解偶联剂羰基氰化物对三氟甲氧基苯腙可使该活性进一步提高3倍,这表明PPA2是能量偶联酶的一部分。利用基因敲除技术,我们发现PPA1是细胞生长所必需的。相比之下,PPA2基因敲除的细胞是活的,但不能在呼吸性碳源上生长。荧光显微镜显示这些细胞已经失去了线粒体DNA。我们得出结论,PPA2编码的线粒体PPase对于线粒体功能和线粒体基因组的维持至关重要。