Campbell V W, Jackson D A
J Biol Chem. 1980 Apr 25;255(8):3726-35.
The effect of different divalent metal ions on the hydrolysis of DNA by DNase I was studied with an assay which distinguishes between cleavage of one or both strands of the DNA substrate during initial encounters between enzyme and DNA. Using covalently closed superhelical SV40(I) DNA as substrate, initial reaction products consisting of relaxed circles or unit-length linears are resolved by electrophoresis of radioactively labeled DNA in agarose gels. Only in the presence of a transition metal ion, such as Mn2+ or Co2+, and only under certain reaction conditions, is DNase I able to cut both DNA strands at or near the same point, generating unit-length linears. This ability to cut both DNA strands is inhibited by such factors as temperature decrease, the addition of a monovalent ion or another divalent cation which is not a transition metal ion, or a reduction in the number of superhelical turns in the DNA substrate. All of these factors lead to a winding of the duplex helix and antagonize the unwinding of the duplex promoted by transition metal ion binding. Transition metal ions may thus convert the DNA substrate locally to a form in which DNase I can introduce breaks into both strands. In the presence of Mg2+, DNase I introduces single strand nicks into SV40(I), generating exclusively the covalently open, relaxed circular SV40(II) as the initial product of the reaction. In the presence of Mn2+, DNase I generates as initial products a mixture of SV40(II) and unit-length SV40 linear DNA molecules, formed by two nicks in opposite strands at or near the same point in the duplex. These circular SV40(II) molecules consist of two types. A minority class is indistinguishable from the nicked SV40(II) produced by DNase I in the presence of Mg2+. The majority class consists of molecules containing a gap in one of the two strands, the mean length of the gap being 11 nucleotides. The SV40(L) molecules produced in the presence of Mn2+ appear to have single strand extensions at one or both ends.
利用一种能区分酶与DNA初次接触时DNA底物单链或双链断裂情况的检测方法,研究了不同二价金属离子对DNase I水解DNA的影响。以共价闭合超螺旋SV40(I)DNA为底物,通过在琼脂糖凝胶中对放射性标记的DNA进行电泳,可分辨出由松弛环或单位长度线性片段组成的初始反应产物。只有在过渡金属离子(如Mn2+或Co2+)存在且仅在特定反应条件下,DNase I才能在同一点或其附近切割DNA的两条链,生成单位长度线性片段。切割两条链的这种能力会受到诸如温度降低、添加一价离子或非过渡金属离子的另一种二价阳离子,或DNA底物中超螺旋匝数减少等因素的抑制。所有这些因素都会导致双链螺旋缠绕,并拮抗由过渡金属离子结合促进的双链解旋。过渡金属离子因此可能将DNA底物局部转化为一种形式,使DNase I能够在两条链中都引入断裂。在Mg2+存在下,DNase I会在SV40(I)中引入单链切口,仅生成共价开放的松弛环状SV40(II)作为反应的初始产物。在Mn2+存在下,DNase I生成的初始产物是SV40(II)和单位长度SV40线性DNA分子的混合物,由双链中同一点或其附近相反链上的两个切口形成。这些环状SV40(II)分子有两种类型。少数类型与在Mg2+存在下由DNase I产生的带切口的SV40(II)无法区分。多数类型由两条链之一中含有缺口的分子组成,缺口的平均长度为11个核苷酸。在Mn2+存在下产生的SV40(L)分子似乎在一端或两端有单链延伸。