Bally M, Foglino M, Bruschi M, Murgier M, Lazdunski A
Eur J Biochem. 1986 Mar 17;155(3):565-9. doi: 10.1111/j.1432-1033.1986.tb09525.x.
The nucleotide sequence of the region probably responsible for regulation of pepN expression and of the region encoding the amino-terminal part of aminopeptidase N, has been determined. The transcription start site was identified by S1 nuclease mapping. All features of the promoter are those of a weak promoter and no obvious structure responsible for regulation was identified, although a possible Pho box is located 63 base pairs upstream from the Pribnow box. The reading frame was unambiguously determined by purifying the protein and by sequencing the first 21 NH2-terminal residues. The NH2-terminal region of aminopeptidase N does not contain any fragment resembling signal sequence and the protein is not produced in a precursor form. A divergent promoter, which might be that of pncB, encoding the nicotinic acid phosphoribosyltransferase (P. Terpstra, personal communication), has also been identified, which allows the assignment of the gene organization in this chromosomal region as ompF asnS pncB pepN.
已经确定了可能负责pepN表达调控的区域以及编码氨肽酶N氨基末端部分的区域的核苷酸序列。通过S1核酸酶作图确定了转录起始位点。启动子的所有特征均表明其为弱启动子,并且未发现负责调控的明显结构,尽管在普里布诺框上游63个碱基对处可能存在一个Pho框。通过纯化蛋白质并对前21个NH2末端残基进行测序,明确确定了阅读框。氨肽酶N的NH2末端区域不包含任何类似于信号序列的片段,并且该蛋白质不是以前体形式产生的。还鉴定出一个可能是编码烟酸磷酸核糖基转移酶的pncB的启动子(P. Terpstra,个人交流),这使得该染色体区域的基因组织可确定为ompF asnS pncB pepN。