Bolland S, Kleckner N
Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.
Proc Natl Acad Sci U S A. 1995 Aug 15;92(17):7814-8. doi: 10.1073/pnas.92.17.7814.
During Tn10 transposition, the element is excised from the donor site by double-strand cleavages at the two transposon ends. Double-strand cleavage is a central step in the nonreplicative transposition reaction of many transposons in both prokaryotes and eukaryotes. Evidence is presented to show that the Tn10 double-strand cut is made by an ordered, sequential cleavage of the two strands. The transferred strand is cut first, and then the nontransferred strand is cleaved. The single-strand nicked intermediate is seen to accumulate when Mn2+ is substituted for Mg2+ in the reaction or when certain mutant transposases are used. The fact that the transferred strand is cleaved before the non-transferred strand implies that the order of strand cleavages is not the determining factor that precludes a replicative mechanism of transposition.
在Tn10转座过程中,该元件通过转座子两端的双链切割从供体位点切除。双链切割是原核生物和真核生物中许多转座子非复制性转座反应的核心步骤。有证据表明,Tn10双链切割是由两条链的有序、顺序切割完成的。转移链先被切割,然后非转移链被切割。当反应中用Mn2+替代Mg2+或使用某些突变转座酶时,可观察到单链切口中间体的积累。转移链在非转移链之前被切割这一事实表明,链切割顺序并非排除转座复制机制的决定性因素。