Mengeritsky G, Trifonov E N
Nucleic Acids Res. 1983 Jun 11;11(11):3833-51. doi: 10.1093/nar/11.11.3833.
The concept of sequence-dependent deformational anisotropy of DNA proposed earlier is further elaborated and a computational procedure is developed for the sequence-directed mapping of the nucleosomes along chromatin DNA nucleotide sequences. The deformational anisotropy is found to be nonuniform along the molecule of the nucleosomal DNA, suggesting that the DNA superhelix in the nucleosome is slightly oval rather than circular in projection. The number of superhelical turns in the nucleosome core particle is estimated to be 2.0 +/- 0.2. Preliminary mapping of the nucleosomes in various chromatin DNA sequences yields the distribution of linker lengths which shows several minima separated by about 10 base-pairs. This is explained by sterical exclusion effects due to overlapping of the nucleosomes in space when some specific linker lengths are chosen. The mapping procedure described is tested by comparing its results with all the most accurate experimental mapping data reported so far. The comparison demonstrates that the exact positions of all the nucleosomes appear to be determined exclusively by the nucleotide sequences.
先前提出的DNA序列依赖性变形各向异性的概念得到了进一步阐述,并开发了一种计算程序,用于沿着染色质DNA核苷酸序列对核小体进行序列定向映射。发现变形各向异性在核小体DNA分子上是不均匀的,这表明核小体中的DNA超螺旋在投影中略呈椭圆形而非圆形。估计核小体核心颗粒中的超螺旋圈数为2.0±0.2。对各种染色质DNA序列中的核小体进行初步映射,得到了连接体长度的分布,该分布显示出几个最小值,间隔约10个碱基对。这是由于在选择某些特定连接体长度时,核小体在空间中重叠而产生的空间排斥效应所解释的。通过将其结果与迄今为止报道的所有最准确的实验映射数据进行比较,对所描述的映射程序进行了测试。比较表明,所有核小体的确切位置似乎完全由核苷酸序列决定。