Topology of Xer recombination on catenanes produced by lambda integrase.
Topology of Xer recombination on catenanes produced by lambda integrase.
复制标题
由 lambda 整合酶产生的索烷上的 Xer 重组拓扑。
DOI:
10.1006/jmbi.1999.2804
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发表时间:
1999
影响因子:
5.6
通讯作者:
S. Colloms
中科院分区:
文献类型:
--
作者:
J. Bath;D. Sherratt;S. Colloms
Xer site-specific recombination at the psi site from plasmid pSC101 displays topological selectivity, such that recombination normally occurs only between directly repeated sites on the same circular DNA molecule. This intramolecular selectivity is important for the biological role of psi, and is imposed by accessory proteins PepA and ArcA acting at accessory DNA sequences adjacent to the core recombination site. Here we show that the selectivity for intramolecular recombination at psi can be bypassed in multiply interlinked catenanes. Xer site-specific recombination occurred relatively efficiently between antiparallel psi sites located on separate rings of right-handed torus catenanes containing six or more nodes. This recombination introduced one additional node into the catenanes. Antiparallel sites on four-noded right-handed catenanes, the normal product of Xer recombination at psi, were not recombined efficiently. Furthermore, parallel psi sites on right-handed torus catenanes were not substrates for Xer recombination. These findings support a model in which psi sites are plectonemically interwrapped, trapping a precise number of supercoils that are converted to four catenation nodes by Xer strand exchange.
影响因子:
4
作者:
Johnson,RC
通讯作者:
Johnson,RC