Stewart F J, Raleigh E A
New England Biolabs, Beverly, MA 01915, USA.
Biol Chem. 1998 Apr-May;379(4-5):611-6.
DNA cleavage by the modification-dependent restriction enzyme McrBC requires the presence of two suitably modified recognition elements appropriately spaced in the substrate. To characterize the spacing requirement in more detail, we have constructed a plasmid with a single McrBC cleavage site, in which the distance between recognition elements could be systematically varied while preserving the local sequence surrounding the recognition elements. Optimal separation between elements was 55-103 basepairs, with detectable cleavage observed at spacing of 32 bp to 2 kb; no cleavage was seen with spacing of 22 bp or less or with 3 kb between elements. Changing the spacing by 4 basepairs within the optimal range had little effect on the efficiency of cleavage, suggesting that the recognition elements need not lie on the same face of the DNA helix.
依赖修饰的限制酶McrBC切割DNA需要在底物中存在两个适当修饰的识别元件,并以适当的间距排列。为了更详细地描述间距要求,我们构建了一个带有单个McrBC切割位点的质粒,其中识别元件之间的距离可以系统地变化,同时保留识别元件周围的局部序列。元件之间的最佳间隔为55 - 103个碱基对,在32 bp至2 kb的间距处可观察到可检测的切割;元件之间间距为22 bp或更小或为3 kb时未观察到切割。在最佳范围内将间距改变4个碱基对,对切割效率影响不大,这表明识别元件不一定位于DNA螺旋的同一面上。