Puhl H L, Behe M J
Department of Chemistry, Lehigh University, Bethlehem, PA 18015.
J Mol Biol. 1993 Feb 20;229(4):827-32. doi: 10.1006/jmbi.1993.1089.
The structure of a 146 base-pair nucleosomal DNA has been probed using hydroxyl radical cleavage in buffers containing NaCl concentrations ranging from 80 mM to 800 mM. The highest salt concentrations used here are close to those required to dissociate core histone H2A and H2B from nucleosomal DNA. Nonetheless, the cleavage pattern of the DNA is unchanged over the tenfold salt concentration range, retaining the approximately 10.0 base-pairs per turn helical periodicity in the flanking regions and approximately 10.7 base-pairs per turn periodicity in the central dyad region that is characteristic of nucleosomal DNA. The rotational frame of the DNA is similarly unaffected by salt. These results support the contention that the differential free energy of bending of DNA around the nucleosome is independent of salt concentration.
在含有80 mM至800 mM氯化钠浓度的缓冲液中,利用羟基自由基切割法对146个碱基对的核小体DNA结构进行了探测。此处使用的最高盐浓度接近使核心组蛋白H2A和H2B与核小体DNA解离所需的浓度。尽管如此,在十倍的盐浓度范围内,DNA的切割模式并未改变,侧翼区域保持着每圈约10.0个碱基对的螺旋周期性,中央二分体区域保持着每圈约10.7个碱基对的周期性,这是核小体DNA的特征。DNA的旋转框架同样不受盐的影响。这些结果支持了这样一种观点,即DNA围绕核小体弯曲的自由能差异与盐浓度无关。