Schricker R, Magdolen V, Kaniak A, Wolf K, Bandlow W
Institut für Genetik und Mikrobiologie, Universität München, Germany.
Gene. 1992 Dec 1;122(1):111-8. doi: 10.1016/0378-1119(92)90038-q.
The gene URA6 encoding uridylate kinase (UK) from Saccharomyces cerevisiae was isolated as a multicopy suppressor of the respiratory-deficient phenotype of an S. cerevisiae mutant defective in the gene AKY2 encoding AMP kinase (AK). The URA6 gene also restored temperature resistance to two different temperature-sensitive mutations in the gene encoding Escherichia coli AK. By contrast, the gene encoding UK of Dictyostelium discoideum on a multicopy yeast shuttle plasmid, expressed under control of the constitutive yeast AKY2 promoter, failed to complement the deficiency in yeast, although such transformants expressed high UK activity. We show that yeast UK exerts significant AK activity which is responsible for the complementation and is absent in the analogous enzyme from D. discoideum. Since UK also significantly phosphorylates CMP (but not GMP), it must be considered an unspecific short-form nucleoside monophosphate kinase. Wild-type mitochondria lack UK activity, but import AKY2. Since multicopy transformation with URA6 heals the Pet- phenotype of AKY2 disruption mutants, the presence of AKY2 in the mitochondrial intermembrane space is not required to maintain respiratory competence. However, furnishing UK with the bipartite intermembrane space-targeting presequence of cytochrome c1 improves the growth rates of AKY2 mutants with nonfermentable substrates, suggesting that AK activity in mitochondria is helpful, though not essential for oxidative growth.
从酿酒酵母中分离出编码尿苷酸激酶(UK)的URA6基因,它是酿酒酵母中一个在编码AMP激酶(AK)的AKY2基因上有缺陷的呼吸缺陷型突变体的多拷贝抑制子。URA6基因还恢复了对编码大肠杆菌AK的基因中两种不同温度敏感突变的温度抗性。相比之下,在组成型酵母AKY2启动子控制下表达的、携带多拷贝酵母穿梭质粒的盘基网柄菌UK基因,虽然这些转化体表达出高UK活性,但未能弥补酵母中的缺陷。我们表明酵母UK发挥着显著的AK活性,这负责了互补作用,而在盘基网柄菌的类似酶中则不存在这种活性。由于UK也能显著磷酸化CMP(但不能磷酸化GMP),它必须被视为一种非特异性的短形式核苷单磷酸激酶。野生型线粒体缺乏UK活性,但能导入AKY2。由于用URA6进行多拷贝转化可修复AKY2破坏突变体的Pet-表型,因此线粒体膜间隙中存在AKY2并非维持呼吸能力所必需。然而,为UK提供细胞色素c1的双膜间隙靶向前序列可提高AKY2突变体利用不可发酵底物的生长速率,这表明线粒体中的AK活性虽对氧化生长不是必需的,但却是有帮助的。