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核心组蛋白的过度乙酰化不会导致核小体解折叠。中子散射数据与核小体的盘状形状相符。

Hyperacetylation of core histones does not cause unfolding of nucleosomes. Neutron scatter data accords with disc shape of the nucleosome.

作者信息

Imai B S, Yau P, Baldwin J P, Ibel K, May R P, Bradbury E M

出版信息

J Biol Chem. 1986 Jul 5;261(19):8784-92.

PMID:3722174
Abstract

Recent studies report that the frictional resistance of partially acetylated core particles increases when the number of acetyl groups/particle exceeds 10 (Bode, J., Gomez-Lira, M. M. & Schröter, H. (1983) Eur. J. Biochem. 130, 437-445). This was attributed to an opening of the core particle though other explanations, e.g. unwinding of the DNA ends were also suggested. Another possible explanation is that release of the core histone N-terminal domains by acetylation increased the frictional resistance of the particle. Neutron scatter studies have been performed on core particles acetylated to different levels up to 2.4 acetates/H4 molecule. Up to this level of acetylation the neutron scatter data show no evidence for unfolding of the core particle. The fundamental scatter functions for the envelope shape and internal structure are identical to those obtained previously for bulk core particles. The structure that gave the best fit to these fundamental scatter functions was a flat disc of diameter 11-11.5 nm and of thickness 5.5-6 nm with 1.7 +/- 0.2 turns of DNA coiled with a pitch of 3.0 nm around a core of the histone octamer. The data analysis emphasizes the changes in pair distance distribution functions at relatively low contrasts, particularly when the protein is contrast matched and DNA dominates the scatter. Under these conditions there is no evidence for the unwinding of long DNA ends in the hyperacetylated core particles. The distance distribution functions go to zero between 11.5 and 12 nm which gives the maximum chord length in a particle of dimension, 11 nm X 5.5 nm. The distance distribution function for the histone octamer contains 85% of the vectors within the 7.0-nm diameter of the histone core. 15% of the histone vectors lie between 7.0 and 12.0 nm, and these are attributed to the N-terminal domains of the core histones which extend out from the central histone core. Histone vectors extending beyond 7.0 nm are necessary to account for the measured radius of gyration of the histone core of 3.3 nm. A similar value of 3.2 nm is calculated for the recent ellipsoidal shape of 11.0 X 6.5 X 6.5 nm from the crystal structure of the octamer. However, the nucleosome model based on this structure is globular, roughly 11 nm in diameter, which does not accord with the flat disc shape core particle obtained from detailed neutron scatter data nor with the cross-section radii of gyration of the histone and DNA found previously for extended chromatin in solution.

摘要

最近的研究报告称,当每个核心颗粒的乙酰基数量超过10时,部分乙酰化核心颗粒的摩擦阻力会增加(博德,J.,戈麦斯 - 利拉,M. M. & 施罗特,H.(1983年)《欧洲生物化学杂志》130卷,437 - 445页)。这被归因于核心颗粒的打开,不过也有人提出了其他解释,例如DNA末端的解旋。另一种可能的解释是,通过乙酰化释放核心组蛋白的N端结构域增加了颗粒的摩擦阻力。已经对乙酰化程度不同直至每个H4分子有2.4个乙酰基的核心颗粒进行了中子散射研究。在这个乙酰化水平之前,中子散射数据没有显示核心颗粒展开的证据。包膜形状和内部结构的基本散射函数与之前对大量核心颗粒获得的函数相同。与这些基本散射函数拟合最佳的结构是一个直径为11 - 11.5纳米、厚度为5.5 - 6纳米的扁平圆盘,有1.7 ± 0.2圈DNA以3.0纳米的螺距围绕组蛋白八聚体核心盘绕。数据分析强调了在相对低对比度下对距离分布函数的变化,特别是当蛋白质与对比度匹配且DNA主导散射时。在这些条件下,没有证据表明高度乙酰化核心颗粒中的长DNA末端会解旋。距离分布函数在11.5至12纳米之间变为零,这给出了尺寸为11纳米×5.5纳米的颗粒中的最大弦长。组蛋白八聚体的距离分布函数包含组蛋白核心直径7.0纳米范围内85%的向量。15% 的组蛋白向量位于7.0至12.0纳米之间,这些归因于从中央组蛋白核心向外延伸的核心组蛋白的N端结构域。延伸超过7.0纳米的组蛋白向量对于解释所测量的组蛋白核心3.3纳米的回转半径是必要的。根据八聚体的晶体结构计算出的最近的11.0×6.5×6.5纳米椭球体形状的回转半径值为3.2纳米。然而,基于这种结构的核小体模型是球形的,直径约为11纳米,这与从详细中子散射数据获得的扁平圆盘形状的核心颗粒不相符,也与之前在溶液中扩展染色质中发现的组蛋白和DNA的横截面回转半径不相符。

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