Landrieu I, Vandenbol M, Härtlein M, Portetelle D
Unité de Microbiologie, Faculté Universitaire des Sciences Agronomiques de Gembloux, Belgium.
Eur J Biochem. 1997 Jan 15;243(1-2):268-73. doi: 10.1111/j.1432-1033.1997.0268a.x.
One of the open reading frames located on yeast Saccharomyces cerevisiae chromosome III, YCR24c, appeared to code for a protein of unknown function, but the predicted sequence showed similarity with asparaginyl-tRNA synthetase from Escherichia coli, with 38% amino acid identity. There is a putative mitochondrial targeting signal at the N-terminus of the YCR24c product. Northern blot analysis of total RNA from a wild-type strain sigma1278b confirmed that YCR24c was transcribed. Disruption of the chromosomal copy of YCR24c in a respiratory-competent haploid cell induced a petite phenotype, but did not affect cell viability. This respiratory-defective phenotype is typical for a mutation in a nuclear gene that induces a non-functional mitochondrial protein synthesis system. The protein encoded by YCR24c was expressed in Escherichia coli in a histidine-tagged form and isolated. The enzyme aminoacylated unfractionated Escherichia coli tRNA with asparagine. These results identified YCR24c as the structural gene for yeast mitochondrial asparaginyl-tRNA synthetase.
位于酵母酿酒酵母Ⅲ号染色体上的一个开放阅读框YCR24c,似乎编码一种功能未知的蛋白质,但预测序列显示与大肠杆菌天冬酰胺-tRNA合成酶相似,氨基酸同一性为38%。YCR24c产物的N端有一个假定的线粒体靶向信号。对野生型菌株sigma1278b的总RNA进行Northern印迹分析证实YCR24c被转录。在具有呼吸能力的单倍体细胞中破坏YCR24c的染色体拷贝会诱导小菌落表型,但不影响细胞活力。这种呼吸缺陷表型是诱导非功能性线粒体蛋白质合成系统的核基因突变的典型表现。YCR24c编码的蛋白质以带组氨酸标签的形式在大肠杆菌中表达并分离出来。该酶用天冬酰胺对未分级的大肠杆菌tRNA进行氨酰化。这些结果确定YCR24c为酵母线粒体天冬酰胺-tRNA合成酶的结构基因。