FitzGerald P C, Simpson R T
J Biol Chem. 1985 Dec 5;260(28):15318-24.
Reassociation of a 260-base pair cloned fragment of Lytechinus variegatus DNA with core histones has been shown to give rise to a uniquely positioned nucleosome (Simpson, R. T., and Stafford, D. W. (1983) Proc. Natl. Acad. Sci. U. S. A. 80, 51-55). In an attempt to define the features that dictate the unique positioning of the nucleosome, we have constructed a number of mutants of this DNA sequence. The ability of these mutants to form positioned nucleosomes was analyzed by DNase I digestion of the DNA after reassociation with chicken erythrocyte core histones. While all the mutants were efficiently incorporated into core particles, not all of these modified sequences were capable of forming a positioned nucleosome. Of the 13 mutants examined, 7 fell into a class that gave rise to nucleosomes in which no unique positioning could be demonstrated. While no specific feature of the DNA sequences has been identified as the critical factor in allowing, or dictating, the formation of positioned nucleosomes, our results do indicate that the region 20-30 bases either side of the center of the core particle appears to contain the major elements necessary for positioning. Additionally, these studies clearly show that differences in the digestion of naked and core particle DNA are related to specific interactions of the DNA and histones rather than to an altered specificity of the enzyme induced by the presence of the proteins.
已证明,将260个碱基对的克隆长刺海胆(Lytechinus variegatus)DNA片段与核心组蛋白重新结合,会产生一个独特定位的核小体(辛普森,R.T.,和斯塔福德,D.W.(1983年)《美国国家科学院院刊》80,51 - 55)。为了确定决定核小体独特定位的特征,我们构建了该DNA序列的多个突变体。在这些突变体与鸡红细胞核心组蛋白重新结合后,通过DNA酶I消化DNA来分析它们形成定位核小体的能力。虽然所有突变体都能有效地整合到核心颗粒中,但并非所有这些修饰后的序列都能形成定位核小体。在所检测的13个突变体中,有7个属于一类,它们产生的核小体无法证明有独特定位。虽然尚未确定DNA序列的任何特定特征是允许或决定形成定位核小体的关键因素,但我们的结果确实表明,核心颗粒中心两侧20 - 30个碱基的区域似乎包含定位所需的主要元件。此外,这些研究清楚地表明,裸露DNA和核心颗粒DNA消化的差异与DNA和组蛋白的特定相互作用有关,而不是与蛋白质存在所诱导的酶的特异性改变有关。