Mirkin S M, Lyamichev V I, Drushlyak K N, Dobrynin V N, Filippov S A, Frank-Kamenetskii M D
Institute of Molecular Genetics, USSR Academy of Sciences, Moscow.
Nature. 1987;330(6147):495-7. doi: 10.1038/330495a0.
Regular homopurine-homopyrimidine tracts, (dG-dA)n(dT-dC)n and (dG)n(dC)n, undergo a superhelix-induced, strongly pH-dependent, structural transition into a novel DNA conformation, the H form. We have suggested that the H form can arise in any homopurine-homopyrimidine mirror repeat (H palindrome). We have now tested this prediction using a tailored series of plasmids carrying the inserts AAGGGAGAAXGGGGTATAGGGGYAAGAGGGAA, where X and Y may be either A or G, and subject them to two-dimensional gel electrophoresis. In support of our hypothesis, the inserts exhibited facile transitions into the H form for X = Y = G, or X = Y = A, whereas the transition was much more difficult or impossible for the two non-palindromes (X = A, Y = G or X = G, Y = A). We present evidence that the H form is the structural basis for S1-nuclease hypersensitivity.
规则的同嘌呤-同嘧啶序列,即(dG-dA)n(dT-dC)n和(dG)n(dC)n,会经历一种由超螺旋诱导的、强烈依赖pH值的结构转变,形成一种新的DNA构象,即H型。我们曾提出,H型可出现在任何同嘌呤-同嘧啶镜像重复序列(H回文序列)中。我们现在使用一系列携带插入片段AAGGGAGAAXGGGGTATAGGGGYAAGAGGGAA的特制质粒来验证这一预测,其中X和Y可以是A或G,并对它们进行二维凝胶电泳。为支持我们的假设,当X = Y = G或X = Y = A时,插入片段能轻易转变为H型,而对于两个非回文序列(X = A,Y = G或X = G,Y = A),这种转变则困难得多或根本不可能。我们提供的证据表明,H型是S1核酸酶超敏反应的结构基础。