Neubauer B, Linxweiler W, Hörz W
J Mol Biol. 1986 Aug 20;190(4):639-45. doi: 10.1016/0022-2836(86)90249-4.
The mechanism underlying sequence-specific positioning of nucleosomes on DNA was investigated. African green monkey alpha-satellite DNA was reconstituted in vitro with histones. Histone octamers were found to adopt one major and several minor positions on the satellite repeat unit, very similar to those positions found previously in vitro, demonstrating that sequence-specific histone-DNA interactions are responsible for nucleosome positioning on this DNA. In order to understand the nature of these interactions in more detail, we have constructed a variant satellite fragment containing an insertion of half a helical DNA turn. The parent fragment directs histones to one major and two overlapping minor positions that are all affected by the insertion. All three frames respond in a unique fashion to the additional five base-pairs. From a quantitative analysis of the nucleosome positions on the engineered fragment, consensus "phasing boxes" as the basis for nucleosome positioning can be ruled out. Instead, our results argue very strongly that nucleosome positioning is due to the independent contribution of many different DNA-histone contacts along the entire core particle, in an apparently additive fashion.
对核小体在DNA上进行序列特异性定位的潜在机制进行了研究。非洲绿猴α卫星DNA在体外与组蛋白进行了重构。发现组蛋白八聚体在卫星重复单元上占据一个主要位置和几个次要位置,这与之前在体外发现的位置非常相似,表明序列特异性的组蛋白-DNA相互作用决定了核小体在该DNA上的定位。为了更详细地了解这些相互作用的本质,我们构建了一个包含半个螺旋DNA转角插入片段的变异卫星片段。亲本片段将组蛋白导向一个主要位置和两个重叠的次要位置,这些位置均受到插入片段的影响。所有三个框架对额外的五个碱基对都以独特的方式做出反应。通过对工程片段上核小体位置的定量分析,可以排除作为核小体定位基础的共有“相位框”。相反,我们的结果有力地表明,核小体定位是由于沿着整个核心颗粒许多不同的DNA-组蛋白接触以明显累加的方式独立起作用的结果。