Kodaira K, Nakano K, Taketo A
Department of Biochemistry I, Fukui Medical School, Japan.
Biochim Biophys Acta. 1989 Apr 12;1007(3):359-62. doi: 10.1016/0167-4781(89)90160-7.
Bacteriophage alpha 3 origin of complementary strand DNA synthesis contains two potential secondary loop structures, I and II, which have been implicated in direct recognition sites for host Escherichia coli dnaG protein. To elucidate the function of the hairpin loops, we have introduced point mutations within the stem of the hairpin II so as to disturb its base-pairings. A mutant, oriAA, which had two point mutations in the region, formed minute plaques on E. coli host cells and its mean burst size at 37 degrees C was about 50, whereas that of wild-type was 250. In addition, the growth of oriAA at 42 degrees C was thermosensitive and the burst size was reduced to 5. From the oriAA, a revertant-like phage oriGA occurred spontaneously with a high-frequency of about 2.10(-2). It retained one point mutation and the plaque size and phage yield were nearly same as those of wild-type. These results are discussed with respect to the role of secondary structure as well as specific nucleotide sequence in the recognition site for the dnaG protein.
噬菌体α3互补链DNA合成的起始位点包含两个潜在的二级环结构,即结构I和结构II,它们被认为是宿主大肠杆菌dnaG蛋白的直接识别位点。为了阐明发夹环的功能,我们在发夹II的茎部引入了点突变,以扰乱其碱基配对。一个在该区域有两个点突变的突变体oriAA,在大肠杆菌宿主细胞上形成微小噬菌斑,其在37℃时的平均裂解量约为50,而野生型的平均裂解量为250。此外,oriAA在42℃时的生长对温度敏感,裂解量降至5。从oriAA中,一种类似回复体的噬菌体oriGA以约2×10⁻²的高频自发出现。它保留了一个点突变,噬菌斑大小和噬菌体产量与野生型几乎相同。针对二级结构以及特定核苷酸序列在dnaG蛋白识别位点中的作用,对这些结果进行了讨论。