Ambrose C, Lowman H, Rajadhyaksha A, Blasquez V, Bina M
Purdue University, Department of Chemistry, West Lafayette, IN 47907.
J Mol Biol. 1990 Aug 20;214(4):875-84. doi: 10.1016/0022-2836(90)90342-J.
Over the past decade, the results of numerous indirect mappings analyses have not clarified whether or not nucleosomes occupy preferred positions in simian virus 40 (SV40) chromatin. To address this question more directly, we followed a shotgun cloning approach and determined the nucleotide sequences of over 400 cloned nucleosomal DNA fragments obtained from digestion of SV40 chromatin with micrococcal nuclease. Our results demonstrate and establish that nucleosomes do not occupy unique positions in SV40 minichromosomes and thus indicate the existence of at least several types of chromatin molecules having different nucleosome organization patterns. We developed two types of statistical analysis in order to examine the cloning data in greater detail. One type, overlap analysis, revealed the distribution of the cloned fragments with respect to SV40 DNA. The distribution exhibits an oscillating pattern, dividing the genome into regions of weak or strong nucleosome density. The other analysis determined the distribution of the midpoints of the cloned fragments and revealed potential strong and weak nucleosome location sites, and an early versus late distinction in organization of nucleosomes in SV40 chromatin. The late region appears to contain more strong nucleosome location sites (8) than the early region (4). The strongest nucleosome abuts the late side of the nuclease-hypersensitive region and includes the major transcription initiation site of the late genes. Another strong site precedes this nucleosome and includes sequences implicated in controlling the expression of the SV40 early and late genes. A strong or weak nucleosome location site is not apparent near the early side of the nucleosome-hypersensitive region. Only weak and overlapping nucleosome location sites are found in the region where replication terminates in the SV40 minichromosomes.
在过去十年中,众多间接图谱分析的结果并未阐明核小体在猴病毒40(SV40)染色质中是否占据优先位置。为了更直接地解决这个问题,我们采用了鸟枪法克隆方法,并确定了从用微球菌核酸酶消化SV40染色质获得的400多个克隆核小体DNA片段的核苷酸序列。我们的结果证明并确定核小体在SV40微型染色体中并不占据独特位置,因此表明至少存在几种具有不同核小体组织模式的染色质分子。我们开发了两种统计分析方法,以便更详细地检查克隆数据。一种是重叠分析,揭示了克隆片段相对于SV40 DNA的分布。该分布呈现出振荡模式,将基因组划分为核小体密度弱或强的区域。另一种分析确定了克隆片段中点的分布,并揭示了潜在的强核小体定位位点和弱核小体定位位点,以及SV40染色质中核小体组织的早期与晚期差异。晚期区域似乎比早期区域(4个)包含更多的强核小体定位位点(8个)。最强的核小体紧靠核酸酶超敏区域的晚期一侧,并包括晚期基因的主要转录起始位点。另一个强位点在这个核小体之前,包括与控制SV40早期和晚期基因表达有关的序列。在核小体超敏区域的早期一侧附近没有明显的强或弱核小体定位位点。在SV40微型染色体中复制终止的区域只发现了弱且重叠的核小体定位位点。