Nordmann P L, Makris J C, Reznikoff W S
Department of Biochemistry, University of Wisconsin-Madison 53706.
Mol Gen Genet. 1988 Sep;214(1):62-7. doi: 10.1007/BF00340180.
Two complementary 24 base single stranded oligonucleotides containing randomly located inosine residues were synthesized in vitro. Once annealed, the two oligonucleotides were cloned into derivatives of ColE1 and transformed into Escherichia coli. Sequence analysis of 157 clones yielded 305 mutations. The pattern of the mutations revealed the following: (1) The frequency of inosine induced mutations was significantly less than predicted from its content in the oligonucleotides; (2) Inosine incorporation resulted almost exclusively in base changes to guanine; (3) The mutation distribution is biased towards A/T to G/C substitutions; (4) There were reproducible position biases; and (5) There was a reproducible strand bias which was independent of the cassette orientation with respect to the plasmid origin of replication.
在体外合成了两条互补的、含有随机分布肌苷残基的24个碱基的单链寡核苷酸。两条寡核苷酸退火后,被克隆到ColE1的衍生物中,并转化到大肠杆菌中。对157个克隆进行序列分析,得到了305个突变。突变模式显示如下:(1) 肌苷诱导的突变频率明显低于根据其在寡核苷酸中的含量所预测的频率;(2) 肌苷掺入几乎只导致碱基变为鸟嘌呤;(3) 突变分布偏向于A/T到G/C的替换;(4) 存在可重复的位置偏向;(5) 存在可重复的链偏向,该偏向与盒式结构相对于质粒复制起点的方向无关。