Izumiya H, Yamamoto M
Department of Biophysics and Biochemistry, School of Science, University of Tokyo, Japan.
J Biol Chem. 1995 Nov 17;270(46):27859-64. doi: 10.1074/jbc.270.46.27859.
We cloned the ndk1 gene encoding a subunit of nucleoside-diphosphate kinase (NDK) from Schizosaccharomyces pombe, by using polymerase chain reaction. The deduced ndk1 gene product has 151 amino acid residues and is approximately 60% identical with both Saccharomyces cerevisiae and mammalian NDKs. The gene product exhibited NDK activity and cross-reacted with antibodies raised against rat NDK. Disruption of ndk1 greatly reduced the cellular NDK activity but caused no obvious phenotype in cell growth and sexual development of the organism. However, a mutated allele of ndk1 could inhibit sexual development in a dominant-negative manner. This allele carried a point mutation in cysteine 116, which locates next to the putative active center histidine 117, and the mutant gene product showed no NDK activity. Gene expression inducible in response to mating pheromone signaling was decreased in cells carrying the dominant-negative allele. Cases have been reported in higher eukaryotes in which NDK appears to play a more sophisticated role than a simple catalyst in cell physiology, and the results of this study suggest that S. pombe NDK may also perform such a role in regulation of sexual development in the fission yeast.
我们利用聚合酶链反应从粟酒裂殖酵母中克隆了编码核苷二磷酸激酶(NDK)一个亚基的ndk1基因。推导的ndk1基因产物有151个氨基酸残基,与酿酒酵母和哺乳动物的NDK均约有60%的同源性。该基因产物表现出NDK活性,并且能与抗大鼠NDK产生的抗体发生交叉反应。ndk1基因的破坏极大地降低了细胞的NDK活性,但在生物体的细胞生长和有性发育中未引起明显的表型。然而,ndk1的一个突变等位基因能够以显性负性方式抑制有性发育。该等位基因在紧邻推定的活性中心组氨酸117的半胱氨酸116处发生了一个点突变,突变的基因产物没有NDK活性。在携带显性负性等位基因的细胞中,响应交配信息素信号诱导的基因表达降低。在高等真核生物中已有报道称NDK在细胞生理学中似乎发挥着比简单催化剂更为复杂的作用,本研究结果表明粟酒裂殖酵母NDK在裂殖酵母有性发育的调控中可能也发挥着这样的作用。