Goryshin I Y, Miller J A, Kil Y V, Lanzov V A, Reznikoff W S
Department of Biochemistry, University of Wisconsin-Madison, 420 Henry Mall, Madison, WI 53706, USA.
Proc Natl Acad Sci U S A. 1998 Sep 1;95(18):10716-21. doi: 10.1073/pnas.95.18.10716.
This communication reports an analysis of Tn5/IS50 target site selection by using an extensive collection of Tn5 and IS50 insertions in two relatively small regions of DNA (less than 1 kb each). For both regions data were collected resulting from in vitro and in vivo transposition events. Since the data sets are consistent and transposase was the only protein present in vitro, this demonstrates that target selection is a property of only transposase. There appear to be two factors governing target selection. A target consensus sequence, which presumably reflects the target selection of individual pairs of Tn5/IS50 bound transposase protomers, was deduced by analyzing all insertion sites. The consensus Tn5/IS50 target site is A-GNTYWRANC-T. However, we observed that independent insertion sites tend to form groups of closely located insertions (clusters), and insertions very often were spaced in a 5-bp periodic fashion. This suggests that Tn5/IS50 target selection is facilitated by more than two transposase protomers binding to the DNA, and, thus, for a site to be a good target, the overlapping neighboring DNA should be a good target, too. Synthetic target sequences were designed and used to test and confirm this model.
本通讯报道了通过对Tn5和IS50在两个相对较小的DNA区域(每个区域小于1 kb)中的大量插入情况进行分析,来研究Tn5/IS50靶位点选择。对于这两个区域,收集了体外和体内转座事件产生的数据。由于数据集是一致的,且体外仅存在转座酶,这表明靶位点选择仅是转座酶的特性。似乎有两个因素决定靶位点选择。通过分析所有插入位点,推导出一个靶共有序列,该序列可能反映了与Tn5/IS50结合的转座酶原聚体对的靶位点选择。Tn5/IS50的共有靶位点是A-GNTYWRANC-T。然而,我们观察到独立的插入位点倾向于形成紧密相邻插入的组(簇),并且插入常常以5 bp的周期方式间隔排列。这表明两个以上的转座酶原聚体与DNA结合有助于Tn5/IS50的靶位点选择,因此,对于一个位点成为良好的靶位点,重叠的相邻DNA也应该是良好的靶位点。设计并使用了合成靶序列来测试和证实该模型。