Halford S E, Lovelady B M, McCallum S A
Gene. 1986;41(2-3):173-81. doi: 10.1016/0378-1119(86)90096-x.
The EcoRV restriction endonuclease normally shows a high specificity for its recognition site on DNA, GATATC. In standard reactions, it cleaves DNA at this site several orders of magnitude more readily than at any alternative sequence. But in the presence of dimethyl sulphoxide and at high pH, the EcoRV enzyme cleaves DNA at several sites that differ from its recognition site by one nucleotide. Of the 18 (3 X 6) possible sequences that differ from GATATC by one base, all were cleaved readily except for the following 4 sites: TATATC, CATATC, GATATA and GATATG. However, two of the sites that could be cleaved by EcoRV in the presence of dimethyl sulphoxide, GAGATC and GATCTC, were only cleaved on DNA that lacked dam methylation: both contain the sequence GATC, the recognition site for the dam methylase of Escherichia coli.
EcoRV限制性内切酶通常对其在DNA上的识别位点GATATC具有高度特异性。在标准反应中,它在该位点切割DNA的速度比在任何其他序列处快几个数量级。但在二甲基亚砜存在且高pH条件下,EcoRV酶会在几个与其识别位点相差一个核苷酸的位点切割DNA。在与GATATC相差一个碱基的18种(3×6)可能序列中,除了以下4个位点:TATATC、CATATC、GATATA和GATATG外,其他所有序列都能被轻易切割。然而,在二甲基亚砜存在下可被EcoRV切割的两个位点GAGATC和GATCTC,仅在缺乏dam甲基化的DNA上被切割:二者都包含序列GATC,即大肠杆菌dam甲基化酶的识别位点。