Taron C H, Van Cott E M, Wilson G G, Moran L S, Slatko B E, Hornstra L J, Benner J S, Kucera R B, Guthrie E P
New England Biolabs, Beverly, MA 01915, USA.
Gene. 1995 Mar 21;155(1):19-25. doi: 10.1016/0378-1119(94)00806-4.
NaeI, a type-II restriction-modification (R-M) system from the bacterium Nocardia aerocolonigenes, recognizes the sequence 5'-GCCGGC. The NaeI DNA methyltransferase (MTase)-encoding gene, naeIM, had been cloned previously in Escherichia coli [Van Cott and Wilson, Gene 74 (1988) 55-59]. However, none of these clones expressed detectable levels of the restriction endonuclease (ENase). The absence of the intact ENase-encoding gene (naeIR) within the isolated MTase clones was confirmed by recloning the MTase clones into Streptomyces lividans. The complete NaeI system was finally cloned using E. coli AP1-200 [Piekarowicz et al., Nucleic Acids Res. 19 (1991) 1831-1835] and less stringent MTase-selection conditions. The naeIR gene was expressed first by cloning into S. lividans, and later by cloning under control of a regulated promoter in an E. coli strain preprotected by the heterologous MspI MTase (M.MspI). The DNA sequence of the NaeI R-M system has been determined, analyzed and compared to previously sequenced R-M systems.
NaeI是一种来自产气诺卡氏菌的II型限制修饰(R-M)系统,可识别序列5'-GCCGGC。NaeI DNA甲基转移酶(MTase)编码基因naeIM此前已在大肠杆菌中克隆出来[范科特和威尔逊,《基因》74(1988年)55 - 59页]。然而,这些克隆体均未表达出可检测水平的限制性内切酶(ENase)。通过将MTase克隆体重组到变铅青链霉菌中,证实了分离出的MTase克隆体内不存在完整的ENase编码基因(naeIR)。最终,利用大肠杆菌AP1 - 200 [皮卡罗维茨等人,《核酸研究》19(1991年)1831 - 1835页]以及不太严格的MTase选择条件,克隆出了完整的NaeI系统。首先通过克隆到变铅青链霉菌中来表达naeIR基因,后来则是在由异源MspI MTase(M.MspI)预先保护的大肠杆菌菌株中,在一个受调控启动子的控制下进行克隆来表达该基因。已确定了NaeI R-M系统的DNA序列,并与之前测序的R-M系统进行了分析和比较。