Pon C L, Calogero R A, Gualerzi C O
Max-Planck-Institut für Molekulare Genetik, Abt. Wittmann, Berlin.
Mol Gen Genet. 1988 May;212(2):199-202. doi: 10.1007/BF00334684.
Beginning with a synthetic oligonucleotide probe derived from its amino acid sequence, we have identified, cloned and sequenced the hns gene encoding H-NS, an abundant Escherichia coli 15 kDa DNA-binding protein with a possible histone-like function. The amino acid sequence of the protein deduced from the nucleotide sequence is in full agreement with that determined for H-NS. By comparison of the restriction map of the cloned gene and of its neighboring regions with the physical map of E. coli K12 as well as by hybridization of the hns gene with restriction fragments derived from the total chromosome, we have located the hns gene oriented counterclockwise at 6.1 min on the E. coli chromosome, just before an IS30 insertion element.
从一个根据其氨基酸序列合成的寡核苷酸探针开始,我们已经鉴定、克隆并测序了编码H-NS的hns基因,H-NS是一种丰富的大肠杆菌15 kDa DNA结合蛋白,可能具有类组蛋白功能。从核苷酸序列推导的该蛋白的氨基酸序列与为H-NS确定的序列完全一致。通过将克隆基因及其相邻区域的限制性图谱与大肠杆菌K12的物理图谱进行比较,以及通过hns基因与来自总染色体的限制性片段杂交,我们已将hns基因定位在大肠杆菌染色体上6.1分钟处,呈逆时针方向,就在一个IS30插入元件之前。