Bi X, Liu L F
Department of Biological Chemistry, Johns Hopkins University, School of Medicine, Baltimore, MD 21205.
J Mol Biol. 1994 Jan 14;235(2):414-23. doi: 10.1006/jmbi.1994.1002.
We show that recombination between directly repeated sequences in plasmids occurs via both recA-independent and recA-dependent mechanisms in Escherichia coli. They are differentially affected by two factors, the distance separating the homologies and the size of the homology. Recombination between tandem duplications up to 300 base-pairs shows virtually no recA dependence. Increasing the size of the duplications beyond 300 base-pairs gradually increases the recA dependence. Furthermore, insertion of a sizable DNA sequence in between the duplications, substantially increases the recA dependence. We conclude that increasing the distance separating the homologous regions preferentially inhibits the recA-independent recombination. On the other hand, shortening of the homology preferentially inhibits recA-dependent recombination. Consequently, recombination between short tandem duplications is totally recA-independent.
我们证明,质粒中直接重复序列之间的重组在大肠杆菌中通过recA非依赖性和recA依赖性机制发生。它们受到两个因素的不同影响,即同源序列之间的间隔距离和同源序列的大小。长达300个碱基对的串联重复序列之间的重组几乎不依赖recA。将重复序列的大小增加到300个碱基对以上会逐渐增加对recA的依赖性。此外,在重复序列之间插入相当大的DNA序列会大幅增加对recA的依赖性。我们得出结论,增加同源区域之间的间隔距离会优先抑制recA非依赖性重组。另一方面,同源序列的缩短会优先抑制recA依赖性重组。因此,短串联重复序列之间的重组完全不依赖recA。