Leach D R, Stahl F W
Nature. 1983;305(5933):448-51. doi: 10.1038/305448a0.
In Escherichia coli in vitro constructions of perfect palindromes larger than 30 base pairs (bp) long have in general been unstable. A perfect palindrome has the unique possibility of forming a cruciform structure, and it is this feature which probably results in its instability. Negative supercoiling favours the formation of the cruciform conformation, which in turn causes the molecule to relax. This relaxation may render replicons containing large perfect palindromes inviable. An alternative hypothesis for inviability has been that the cruciform interferes with replication by favouring strand switching by polymerase I. Here we show that the simultaneous absence of two recombination nucleases, the recBC product, exonuclease V, and the sbcB product, exonuclease I, confers viability on a derivative of phage lambda carrying a perfect palindrome of inverted repeat length 1,600 bases. This observation suggests a third hypothesis--that nucleolytic cleavage of the cruciform is responsible for the inviability of the phage. Such an activity has been shown in vitro for T4 exonuclease VII.
在大肠杆菌中,体外构建长度超过30个碱基对(bp)的完美回文序列通常是不稳定的。完美回文序列具有形成十字形结构的独特可能性,正是这一特征可能导致其不稳定。负超螺旋有利于十字形构象的形成,这反过来又会使分子松弛。这种松弛可能会使含有大的完美回文序列的复制子无法存活。关于无法存活的另一种假说是,十字形通过促进聚合酶I的链交换来干扰复制。在这里,我们表明,同时缺失两种重组核酸酶,即recBC产物核酸外切酶V和sbcB产物核酸外切酶I,可使携带长度为1600个碱基的反向重复序列的完美回文序列的λ噬菌体衍生物具有生存能力。这一观察结果提出了第三种假说——十字形的核酸酶切导致噬菌体无法存活。体外实验已证明T4核酸外切酶VII具有这种活性。