Simpson R T, Bustin M
Biochemistry. 1976 Sep 21;15(19):4305-12. doi: 10.1021/bi00664a026.
Chromatin subunits were prepared from HeLa cells by in situ digestion of nuclear DNA with micrococcal nuclease followed by sucrose gradient sedimentation. These 11S chromosomal particles (nucleosomes) contain a DNA fragment 140--180 base pairs long and an equal mass of histones, H2A, H2B, H3, and h4. nucleosomes were incubated with purified antibodies to histones H2A and H2B and to hemoglobin A, and the resulting complexes were analyzed by ultracentrifugation. Of these, only anti-H2B bound specifically to nucleosomes. When sufficient antibody was present, all (greater than 98%) the nucleosomes sedimented with increased velocities, indicating that all chromosomal particles contain H2B, as suggested by previous electron microscopic studies (Bustin, M., Goldblatt, D., and Sperling, R. (1976), Cell 7, 297). The amount of antibody reacting with H2B in the nucleosome was quantitated by densitometric scanning of gel electrophoresis patterns of the proteins in various nucleosome-anti-H2B complexes separated by sedimentation on isokinetic sucrose gradients. Under conditions where all particles had increased sedimentation velocities, from 1 to 3 IgG molecules are bound to each nucleosome, the ratio increasing from top to bottom of the sedimenting peak. When nucleosomes are thus dispersed on the basis of reaction with anti-H2B, the ratios of H2A to H4 and of (H2B + H3) to H4 are identical (+/- 8%) for all fractions, suggesting that each nucleosome has an identical histone complement, two each of histones H2A, H2B, H3, and H4. Confidence limits for exclusion of other possible octamers are presented. The variation in ratio of bound antibody to nucleosome probably reflects a normal distribution during the titration, although differential exposure of H2B antigenic determinants in several populations of nucleosomes cannot be excluded as an explanation. The method use should be generally applicable to further studies of the composition and function of nucleosomes.
通过用微球菌核酸酶原位消化核DNA,随后进行蔗糖梯度沉降,从HeLa细胞中制备染色质亚基。这些11S染色体颗粒(核小体)包含一个140 - 180个碱基对长的DNA片段以及等量的组蛋白H2A、H2B、H3和H4。将核小体与针对组蛋白H2A和H2B以及血红蛋白A的纯化抗体一起温育,然后通过超速离心分析所得复合物。其中,只有抗H2B特异性结合核小体。当存在足够的抗体时,所有(大于98%)核小体沉降速度加快,表明所有染色体颗粒都含有H2B,正如先前电子显微镜研究(Bustin, M., Goldblatt, D., and Sperling, R. (1976), Cell 7, 297)所表明的那样。通过对在等速蔗糖梯度上沉降分离的各种核小体 - 抗H2B复合物中的蛋白质进行凝胶电泳图谱的光密度扫描,对核小体中与H2B反应的抗体量进行定量。在所有颗粒沉降速度都增加的条件下,每个核小体结合1至3个IgG分子,该比例从沉降峰的顶部到底部逐渐增加。当根据与抗H2B的反应将核小体分散时,所有组分中H2A与H4以及(H2B + H3)与H4的比例相同(±8%),这表明每个核小体具有相同的组蛋白组成,即组蛋白H2A、H2B、H3和H4各两个。给出了排除其他可能八聚体的置信限。结合抗体与核小体比例的变化可能反映了滴定过程中的正态分布,尽管不能排除几种核小体群体中H2B抗原决定簇的差异暴露作为一种解释。所使用的方法应普遍适用于核小体组成和功能的进一步研究。