Malanowska Karolina, Yoneji Sumiko, Salyers Abigail A, Gardner Jeffrey F
Department of Microbiology, University of Illinois, Urbana, IL61801, USA.
Nucleic Acids Res. 2007;35(17):5861-73. doi: 10.1093/nar/gkm637. Epub 2007 Aug 24.
Although the integrase (IntDOT) of the Bacteroides conjugative transposon CTnDOT has been classified as a member of the tyrosine recombinase family, the reaction it catalyzes appears to differ in some features from reactions catalyzed by other tyrosine recombinases. We tested the ability of IntDOT to cleave and ligate activated attDOT substrates in the presence of mismatches. Unlike other tyrosine recombinases, the results revealed that IntDOT is able to perform ligation reactions even when all the bases within the crossover region are mispaired. We also show that there is a strong bias in the order of strand exchanges during integrative recombination. The top strands are exchanged first in reactions that appear to require 2 bp of homology between the partner sites adjacent to the sites of cleavage. The bottom strands are exchanged next in reactions that do not require homology between the partner sites. This mode of coordination of strand exchanges is unique among tyrosine recombinases.
尽管拟杆菌属接合转座子CTnDOT的整合酶(IntDOT)已被归类为酪氨酸重组酶家族的成员,但其催化的反应在某些特征上似乎与其他酪氨酸重组酶催化的反应有所不同。我们测试了IntDOT在错配存在的情况下切割和连接活化的attDOT底物的能力。与其他酪氨酸重组酶不同,结果显示IntDOT即使在交叉区域内的所有碱基都错配时也能够进行连接反应。我们还表明,在整合重组过程中,链交换的顺序存在强烈的偏向性。在似乎需要切割位点相邻的配对位点之间有2个碱基对同源性的反应中,首先交换顶部链。在配对位点之间不需要同源性的反应中,接下来交换底部链。这种链交换的协调模式在酪氨酸重组酶中是独特的。