O'Connor M B, Malamy M H
J Bacteriol. 1983 Nov;156(2):669-79. doi: 10.1128/jb.156.2.669-679.1983.
We have discovered a new insertion sequence, now designated IS121, as a component of the Mu dI1 (Ap lac) phage. This sequence is 1.2 kilobases long and contains single recognition sites for the HincII, Bg1II, and HindIII restriction endonucleases. IS121 is present in at least three copies in the chromosome of several Escherichia coli K-12 strains. When present in the nonconjugative plasmid pBR322, IS121 can mediate cointegrate formation with an F' lac plasmid and transfer of pBR322 sequences to suitable recipients. IS121 is also capable of precise or nearly precise excision. As part of the study of IS121, we have determined the physical structure of the Mu dI1 (Ap lac) phage and established an extensive restriction endonuclease map of this phage. A revised schema for the formation of the Mu dI1 (Ap lac) phage is presented.
我们发现了一种新的插入序列,现命名为IS121,它是Mu dI1(Ap lac)噬菌体的一个组成部分。该序列长1.2千碱基,含有HincII、Bg1II和HindIII限制性内切酶的单一识别位点。IS121在几种大肠杆菌K-12菌株的染色体中至少以三个拷贝存在。当存在于非接合性质粒pBR322中时,IS121可介导与F' lac质粒形成共整合体,并将pBR322序列转移至合适的受体。IS121也能够进行精确或近乎精确的切除。作为对IS121研究的一部分,我们确定了Mu dI1(Ap lac)噬菌体的物理结构,并建立了该噬菌体的详细限制性内切酶图谱。本文还提出了Mu dI1(Ap lac)噬菌体形成的修订模式。