Yaneva M, Busch H
Biochemistry. 1986 Sep 9;25(18):5057-63. doi: 10.1021/bi00366a013.
Digestion of HeLa cell nuclei with micrococcal nuclease or deoxyribonuclease I (DNase I) released the 86-kilodalton-70-kilodalton (kDa) protein complex in particles sedimenting at approximately 10 S in sucrose density gradients. Immunoaffinity-purified 32P-labeled complexes contained 86- and 70-kDa polypeptides with phosphorylated serine residues and DNA fragments, of which the largest was 110 base pairs long. Digestion of nick-translated nuclei with micrococcal nuclease released 32P-labeled 10S particles that were immunoaffinity-purified; they contained labeled 110-base-pair DNA fragments. The micrococcal nuclease digests were analyzed by two-dimensional electrophoresis, which separated nucleosomes in the first dimension and the associated proteins in the second. Western blots of the separated proteins showed that the 86-kDa-70-kDa complex was associated with the mono-, di-, and trinucleosomes. A more extensive electrophoretic separation revealed that the 10S particle from nick-translated nuclei migrated with a subfraction of the mononucleosomes that lacked H1 histones. These results suggest that the 10S particle which contains the 86-kDa-70-kDa complex is associated with an unfolded nucleosome that is present in DNase I sensitive regions.
用微球菌核酸酶或脱氧核糖核酸酶I(DNase I)消化HeLa细胞核,可在蔗糖密度梯度中约10 S沉降的颗粒中释放出86千道尔顿-70千道尔顿(kDa)的蛋白质复合物。免疫亲和纯化的32P标记复合物包含带有磷酸化丝氨酸残基的86 kDa和70 kDa多肽以及DNA片段,其中最大的片段长110个碱基对。用微球菌核酸酶消化缺口平移的细胞核可释放出经免疫亲和纯化的32P标记的10S颗粒;它们包含标记的110碱基对DNA片段。通过二维电泳分析微球菌核酸酶消化产物(在第一维中分离核小体,在第二维中分离相关蛋白质)。对分离出的蛋白质进行的蛋白质印迹分析表明,86 kDa-70 kDa复合物与单核小体、双核小体和三核小体相关。更广泛的电泳分离显示,来自缺口平移细胞核的10S颗粒与缺乏H1组蛋白的单核小体亚组分一起迁移。这些结果表明,含有86 kDa-70 kDa复合物的10S颗粒与存在于DNase I敏感区域的未折叠核小体相关。