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Modelling and DNA topology of compact 2-start and 1-start chromatin fibres

机译:紧凑型2起点和1起点染色质纤维的建模和DNA拓扑

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摘要

We have investigated the structure of the most compact 30-nm chromatin fibres by modelling those with 2-start or 1-start crossed-linker organisations. Using an iterative procedure we obtained possible structural solutions for fibres of the highest possible compaction permitted by physical constraints, including the helical repeat of linker DNA. We find that this procedure predicts a quantized nucleosome repeat length (NRL) and that only fibres with longer NRLs (≥197 bp) can more likely adopt the 1-start organisation. The transition from 2-start to 1-start fibres is consistent with reported differing binding modes of the linker histone. We also calculate that in 1-start fibres the DNA constrains more torsion (as writhe) than 2-start fibres with the same NRL and that the maximum constraint obtained is in accord with previous experimental results. We posit that the coiling of the fibre is driven by overtwisting of linker DNA which, in the most compact forms - for example, in echinoderm sperm and avian erythrocytes - could adopt a helical repeat of ∼10 bp/turn. We argue that the total twist of linker DNA could be modulated by interaction with other abundant chromatin-associated proteins and by epigenetic modifications of the C-terminal tail of linker histones.
机译:我们通过对具有2个起点或1个起点的交联接头组织的模型进行建模,研究了最紧凑的30 nm染色质纤维的结构。使用迭代过程,我们获得了物理约束(包括连接子DNA的螺旋重复)所允许的具有最高可能压实度的纤维的可能结构解决方案。我们发现,此程序可预测定量的核小体重复长度(NRL),只有具有更长NRL(≥197bp)的纤维才更有可能采用1-start组织。从2-起始纤维到1-起始纤维的转变与接头组蛋白的报道的不同结合模式一致。我们还计算出,与具有相同NRL的2根起始纤维相比,在1根起始纤维中DNA约束的扭曲(扭曲)更大,并且获得的最大约束与先前的实验结果一致。我们认为,纤维的卷曲是由接头DNA的过度缠绕驱动的,接头DNA以最紧凑的形式-例如,在棘皮动物的精子和禽类红细胞中-可以采用大约10 bp /圈的螺旋重复。我们认为,通过与其他丰富的染色质相关蛋白的相互作用以及连接蛋白组蛋白C末端尾部的表观遗传修饰,可以调节连接蛋白DNA的总扭曲。

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