Levy-Wilson B, Fortier C, Blackhart B D, McCarthy B J
Gladstone Foundation Laboratories for Cardiovascular Disease, University of California, San Francisco 94140-0608.
Mol Cell Biol. 1988 Jan;8(1):71-80. doi: 10.1128/mcb.8.1.71-80.1988.
We have mapped the DNase I- and micrococcal nuclease-hypersensitive sites present in the 5' end of the human apolipoprotein B (apo-B) gene in nuclei from cells expressing or not expressing the gene. Four DNase I-hypersensitive sites were found in nuclei from liver-derived HepG2 cells and intestine-derived CaCo-2 cells, which express the apo-B gene, but not in HeLa cells, which do not. These sites are located near positions -120, -440, -700, and +760 base pairs relative to the transcriptional start site. Undifferentiated CaCo-2 cells exhibited another site, near position -540. Six micrococcal nuclease-hypersensitive sites were found in nuclei from HepG2 and CaCo-2 cells, but not in HeLa cells or free DNA. These sites are located near positions -120, -390, -530, -700, -850, and +210. HepG2 cells exhibited another site, near position +460. Comparison of the DNA sequence of the 5' flanking regions of the human and mouse apo-B genes revealed a high degree of evolutionary conservation of short stretches of sequences in the immediate vicinity of each of the DNase I- and most of the micrococcal nuclease-hypersensitive sites.
我们已绘制出人类载脂蛋白B(apo-B)基因5'端存在的DNA酶I和微球菌核酸酶超敏位点图谱,这些图谱来自表达或不表达该基因的细胞的细胞核。在表达apo-B基因的源自肝脏的HepG2细胞和源自肠道的CaCo-2细胞的细胞核中发现了四个DNA酶I超敏位点,但在不表达该基因的HeLa细胞中未发现。这些位点相对于转录起始位点位于约-120、-440、-700和+760碱基对的位置附近。未分化的CaCo-2细胞在约-540位置处表现出另一个位点。在HepG2和CaCo-2细胞的细胞核中发现了六个微球菌核酸酶超敏位点,但在HeLa细胞或游离DNA中未发现。这些位点位于约-120、-390、-530、-700、-850和+210的位置附近。HepG2细胞在约+460位置处表现出另一个位点。对人类和小鼠apo-B基因5'侧翼区域的DNA序列进行比较后发现,在每个DNA酶I超敏位点和大多数微球菌核酸酶超敏位点紧邻区域的短序列片段具有高度的进化保守性。