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序列非依赖性重组三链螺旋:一项分子动力学研究。

Sequence-independent recombination triple helices: a molecular dynamics study.

作者信息

Kiran M R, Bansal M

机构信息

Molecular Biophysics Unit, Indian Institute of Science, Bangalore, India.

出版信息

J Biomol Struct Dyn. 1997 Oct;15(2):333-45. doi: 10.1080/07391102.1997.10508196.

Abstract

Recent experimental studies have shown that the Rec-A mediated homologous recombination reaction involves a triple helical intermediate, in which the third strand base forms hydrogen bonds with both the bases in the major groove of the Watson-Crick duplex. Such 'mixed' hydrogen bonds allow formation of sequence independent triplexes. DNA triple helices involving 'mixed' hydrogen bonds have been studied, using model building, molecular mechanics (MM) and molecular dynamics (MD). Models were built for a triplex comprising all four possible triplets viz., G.CC, C.GG, A.TT and T.AA. To check the stability of all the 'mixed' hydrogen bonds in such triplexes and the conformational preferences of such triplex structures, MD studies were carried out starting from two structures with 30 degrees and 36 degrees twist between the basepairs. It was observed that though the two triplexes converged towards a similar structure, the various hydrogen bonds between the WC duplex and the third strand showed differential stabilities. An MD simulation with restrained hydrogen bonds showed that the resulting structure was stable and remained close to the starting structure. These studies help us in defining stable hydrogen bond geometries involving the third strand and the WC duplex. It was observed that in the C.GG triplets the N7 atom of the second strand is always involved in hydrogen bonding. In the G.CC triplets, either N3 or O2 in the third strand cytosine can interchangeably act as a hydrogen bond acceptor.

摘要

最近的实验研究表明,Rec - A介导的同源重组反应涉及一种三螺旋中间体,其中第三条链的碱基与沃森-克里克双链体大沟中的两个碱基都形成氢键。这种“混合”氢键允许形成不依赖序列的三链体。利用模型构建、分子力学(MM)和分子动力学(MD)对涉及“混合”氢键的DNA三螺旋进行了研究。构建了包含所有四种可能三联体的三链体模型,即G.CC、C.GG、A.TT和T.AA。为了检验此类三链体中所有“混合”氢键的稳定性以及此类三链体结构的构象偏好,从碱基对之间扭转角度为30度和36度的两种结构开始进行分子动力学研究。观察到尽管这两种三链体趋向于形成相似的结构,但沃森-克里克双链体与第三条链之间的各种氢键表现出不同的稳定性。一项对氢键进行约束的分子动力学模拟表明,所得结构是稳定的,并且与起始结构保持接近。这些研究有助于我们确定涉及第三条链和沃森-克里克双链体的稳定氢键几何结构。观察到在C.GG三联体中,第二条链的N7原子总是参与氢键形成。在G.CC三联体中,第三条链胞嘧啶中的N3或O2可以互换地作为氢键受体。

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