Reczek P R, Weissman D, Hüvös P E, Fasman G D
Biochemistry. 1982 Mar 2;21(5):993-1002. doi: 10.1021/bi00534a026.
Postsynthetic modifications of core histones by treatment of HeLa S3 cells with 5mM sodium butyrate lead to alterations in the structure of high molecular weight chromatin. Whole chromatin from butyrate-treated cells, which results in highly acetylated core histones, has an ellipticity [theta]282.5 of 3700 deg cm2 dmol-1 (0.2 mM EDTA, pH 7.4) that is 1200 deg c m2 dmol-1 less than chromatin from untreated HeLa cells, suggesting a more condensed structure. No difference in the circular dichroism spectra was observed in H1-stripped, high molecular weight chromatin obtained from control and butyrate-treated cells at low (0.2 mM EDTA, pH 7.4) ionic strength. Thermal denaturation profiles of high molecular weight chromatin were resolved into three transitions and exhibited a shifting of hyperchromicity from transition I to transitions III, at a higher Tm, with butyrate treatment of HeLa cells, further indicating a more compact structure. Thermal denaturation profiles of H1-stripped chromatin were not affected by butyrate treatment. Ionic strength studies in the range of 0-5 mM NaH2PO4, 0.2 mM EDTA, pH 7.4, of high molecular weight chromatin exhibited a decrease in [theta]282.5 and a shifting of hyperchromicity from transition I to transition III with increasing ionic strength. Control high molecular weight chromatin was more sensitive to changes in ionic strength than its highly acetylated counterpart. These results suggest that acetylation of histones alone does not result in a change in histone-DNA interactions but other changes associated with butyrate treatment most probably cause a more condensed structure, of the fraction studied herein, which is mediated by H1 or other materials removed during stripping in 0.35 M NaCl.
用5mM丁酸钠处理HeLa S3细胞对核心组蛋白进行合成后修饰,会导致高分子量染色质结构发生改变。来自丁酸钠处理细胞的全染色质,其核心组蛋白高度乙酰化,在0.2 mM EDTA(pH 7.4)条件下,椭圆率[θ]282.5为3700度·厘米²·dmol⁻¹,比未处理的HeLa细胞的染色质低1200度·厘米²·dmol⁻¹,表明其结构更紧密。在低离子强度(0.2 mM EDTA,pH 7.4)下,从对照细胞和丁酸钠处理细胞中获得的H1去除的高分子量染色质的圆二色光谱未观察到差异。HeLa细胞经丁酸钠处理后,高分子量染色质的热变性曲线解析为三个转变,并在较高的熔解温度下,增色现象从转变I转移到转变III,进一步表明结构更紧凑。H1去除的染色质的热变性曲线不受丁酸钠处理的影响。在0 - 5 mM NaH₂PO₄、0.2 mM EDTA(pH 7.4)范围内对高分子量染色质进行离子强度研究,结果显示随着离子强度增加,[θ]282.5降低,增色现象从转变I转移到转变III。对照高分子量染色质比其高度乙酰化的对应物对离子强度变化更敏感。这些结果表明,仅组蛋白乙酰化不会导致组蛋白 - DNA相互作用发生变化,但与丁酸钠处理相关的其他变化很可能导致本文研究部分的结构更紧密,这是由H1或在0.35 M NaCl去除过程中去除的其他物质介导的。