An W, Leuba S H, van Holde K, Zlatanova J
Department of Biochemistry and Biophysics, Oregon State University, Corvallis, OR 97331-7305, USA.
Proc Natl Acad Sci U S A. 1998 Mar 31;95(7):3396-401. doi: 10.1073/pnas.95.7.3396.
The protection against micrococcal nuclease digestion afforded to chromatosomal DNA by the presence of a linker histone (H1(o)) has been quantitatively measured in two reconstituted systems. We have used chromatosomes reconstituted at two distinct positions on a DNA fragment containing the 5S rRNA gene from Lytechinus variegatus and at a specific position on a sequence containing Gal4- and USF-binding sites. In all cases, we find asymmetric protection, with approximately 20 bp protected on one side of the core particle and no protection on the other. We demonstrated through crosslinking experiments that the result is not due to any sliding of the histone core caused by either linker histone addition or micrococcal nuclease cleavage. Because the core particle is itself a symmetric object, the preferred asymmetric location of a linker histone must be dictated by unknown elements in the DNA sequence.
在两个重构系统中,对连接组蛋白(H1(o))存在时赋予染色体DNA免受微球菌核酸酶消化的保护作用进行了定量测量。我们使用了在来自多棘海胆的5S rRNA基因的DNA片段上两个不同位置重构的染色质小体,以及在含有Gal4和USF结合位点的序列上的一个特定位置重构的染色质小体。在所有情况下,我们都发现了不对称保护,在核心颗粒的一侧约有20 bp受到保护,而另一侧则没有保护。我们通过交联实验证明,该结果不是由于连接组蛋白添加或微球菌核酸酶切割导致的组蛋白核心的任何滑动所致。由于核心颗粒本身是一个对称物体,连接组蛋白的首选不对称位置必定由DNA序列中的未知元件决定。