Nishigaki K, Kaneko Y, Wakuda H, Husimi Y, Tanaka T
Nucleic Acids Res. 1985 Aug 26;13(16):5747-60. doi: 10.1093/nar/13.16.5747.
Restriction endonucleases (13 out of 18 species used for the test) were certified to cleave single-stranded(ss)DNA. Such enzymes as AvaII, HaeII, DdeI, AluI, Sau3AI, AccII,TthHB8I and HapII were newly reported to cleave ssDNA. A model to account for the cleavage of ssDNA by restriction enzymes was proposed with supportive data. The essential part of the model was that restriction enzymes preferentially cleave transiently formed secondary structures (called canonical structures) in ssDNA composed of two recognition sequences with two fold rotational symmetry. This means that a restriction enzyme can cleave ssDNAs in general so far as the DNAs have the sequences of restriction sites for the enzyme, and that the rate of cleavage depends on the stabilities of canonical structures.
限制性核酸内切酶(用于测试的18种酶中有13种)经鉴定可切割单链(ss)DNA。诸如AvaII、HaeII、DdeI、AluI、Sau3AI、AccII、TthHB8I和HapII等酶是新报道的可切割ssDNA的酶。提出了一个解释限制性酶切割ssDNA的模型并给出了支持数据。该模型的关键部分是,限制性酶优先切割由具有双重旋转对称性的两个识别序列组成的ssDNA中瞬时形成的二级结构(称为规范结构)。这意味着,一般而言,只要DNA具有该酶的限制酶切位点序列,限制性酶就能切割ssDNA,并且切割速率取决于规范结构的稳定性。