Deonier R C, Oh G R, Hu M
J Bacteriol. 1977 Feb;129(2):1129-40. doi: 10.1128/jb.129.2.1129-1140.1977.
The sequence organization of the F-prime ORF203 was determined by heteroduplex analysis. This large, type II F-prime (Scaife, 1967) contains lac, proC, and purE genes derived from the W1485 subline of Escherichia coli K-12. The IS3 and IS2 elements previously found in the lac-proC-purE region derived from the 58-161 subline (Hu et al., 1975) are also present in the same locations in the bacterial deoxyribonucleic acid (DNA) from the W1485 subline. Recombination between the IS2 region of F and an IS2 element located between lac and proC on the bacterial DNA apparently led to the formation of the perental Hfr, OR21. IS2 is thus directly repeated, with one copy of each element appearing at each of the two junctions between F and the bacterial sequences on ORF203. The F plasmid is found together with ORF203 in the plasmid DNA, and this probably forms from ORF203 by recombination between the directly repeated IS2 elements. ORF203 appears to have been excised from the Hfr chromosome by recombination between the IS3 sequence alpha3beta3 located counterclockwise of lac and the directly repeated IS3 sequence alpha4beta4 located clockwise of purE.
通过异源双链分析确定了F-prime ORF203的序列组织。这个大型的II型F-prime(斯卡菲,1967)包含来自大肠杆菌K-12 W1485亚系的lac、proC和purE基因。先前在来自58-161亚系(胡等人,1975)的lac-proC-purE区域中发现的IS3和IS2元件,在来自W1485亚系的细菌脱氧核糖核酸(DNA)的相同位置也存在。F的IS2区域与位于细菌DNA上lac和proC之间的一个IS2元件之间的重组显然导致了亲本Hfr OR21的形成。因此,IS2是直接重复的,每个元件的一个拷贝出现在ORF203上F与细菌序列之间的两个连接处的每一个。F质粒与ORF203一起存在于质粒DNA中,这可能是由直接重复的IS2元件之间的重组从ORF203形成的。ORF203似乎是通过位于lac逆时针方向的IS3序列alpha3beta3与位于purE顺时针方向的直接重复IS3序列alpha4beta4之间的重组从Hfr染色体上切除的。