Loppes R, Michels R, Decroupette I, Joris B
Laboratory of Molecular Genetics, University of Liège, Belgium.
Curr Genet. 1991 Apr;19(4):255-60. doi: 10.1007/BF00355051.
The complete nucleotide sequence of the ARG7 gene, coding for argininosuccinate lyase (EC 4.3.2.1), in the fission yeast (Schizosaccharomyces pombe) has been determined. It consists of an open reading frame of 461 codons. The deduced protein has a molecular weight of 51,200 Da. The gene is devoid of introns which is confirmed by the fact that it is expressed in Escherichia coli after spontaneous insertion of a bacterial sequence probably bearing a prokaryotic promoter. A perfect "TATA" box is found at -72 and the major transcription initiation site in Saccharomyces cerevisiae is located at -11 as shown by primer extension experiments. Comparison of the S. pombe lyase with related proteins from other organisms reveals an important degree of conservation except in the carboxyterminal part of the polypeptide. Additionally, a deletion removing 66 amino acids of the carboxy terminus yields an enzyme exhibiting some biological activity. A unique 1,500 b transcript was found in S. cerevisiae when the intact gene was present, but the deleted version of the gene gave rise to at least three transcripts of 1,800, 2,800 and 3,900 b.
已确定裂殖酵母(粟酒裂殖酵母)中编码精氨琥珀酸裂解酶(EC 4.3.2.1)的ARG7基因的完整核苷酸序列。它由一个461个密码子的开放阅读框组成。推导的蛋白质分子量为51,200道尔顿。该基因没有内含子,这一点通过以下事实得到证实:在自发插入一个可能带有原核启动子的细菌序列后,它在大肠杆菌中表达。在-72处发现一个完美的“TATA”框,引物延伸实验表明,酿酒酵母中的主要转录起始位点位于-11处。粟酒裂殖酵母裂解酶与其他生物体相关蛋白质的比较显示,除了多肽的羧基末端部分外,存在重要程度的保守性。此外,缺失羧基末端66个氨基酸产生一种具有一定生物活性的酶。当完整基因存在时,在酿酒酵母中发现了一种独特的1500碱基转录本,但该基因的缺失版本产生了至少三种分别为1800、2800和3900碱基的转录本。