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Entropic effect of macromolecular crowding enhances binding between nucleosome clutches in heterochromatin but not in euchromatin

机译:大分子拥挤的熵效应增强了异染色质中核小体离合器之间的结合但常染色质中没有

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摘要

Sharp increase in macromolecular crowding induces abnormal chromatin compaction in the cell nucleus, suggesting its non-negligible impact on chromatin structure and function. However, the details of the crowding-induced chromatin compaction remain poorly understood. In this work, we present a computer simulation study on the entropic effect of macromolecular crowding on the interaction between chromatin structural units called nucleosome clutches. Nucleosome clutches were modeled by a chain of nucleosomes collapsed by harmonic restraints implicitly mimicking the nucleosome association mediated by histone tails and linker histones. The nucleosome density of the clutches was set close to either that of high-density heterochromatin or that of low-density euchromatin. The effective interactions between these nucleosome clutches were calculated in various crowding conditions, and it was found that the increase in the degree of macromolecular crowding induced attractive interaction between two clutches with high nucleosome density. Interestingly, the increased degree of macromolecular crowding did not induce any attraction between two clutches with low nucleosome density. Our results suggest that the entropic effect of macromolecular crowding can enhance binding between nucleosome clutches in heterochromatin, but not in euchromatin, as a result of the difference in nucleosome packing degrees.
机译:大分子拥挤的急剧增加会引起细胞核中染色质的异常紧实,表明其对染色质结构和功能的影响不可忽略。然而,拥挤诱导的染色质压实的细节仍然知之甚少。在这项工作中,我们提供了一个计算机模拟研究,研究大分子拥挤对染色质结构单元(称为核小体离合体)之间相互作用的熵效应。核小体的离合器是由一串核小体建模的,核小体的链因谐波限制而折叠,隐含地模仿了由组蛋白尾巴和接头组蛋白介导的核小体缔合。离合器的核小体密度设置为接近高密度异染色质或低密度常染色质的密度。在各种拥挤条件下计算了这些核小体离合器之间的有效相互作用,发现大分子拥挤程度的增加诱导了两个具有高核小体密度的离合器之间的有吸引力的相互作用。有趣的是,大分子拥挤程度的提高并未在两个核小体密度低的离合器之间引起任何吸引力。我们的研究结果表明,由于核小体堆积程度的不同,大分子拥挤的熵效应可以增强异染色质中核小体离合器之间的结合,而常染色质中不能增强。

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