Department of Chemistry, Seoul National University, Seoul, 08826, Republic of Korea.
Department of Chemistry and Nanoscience, Ewha Womans University, Seoul, 03760, Republic of Korea.
Sci Rep. 2018 Apr 3;8(1):5469. doi: 10.1038/s41598-018-23753-0.
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.
大分子拥挤的急剧增加会导致细胞核中染色质的异常紧缩,表明其对染色质结构和功能具有不可忽视的影响。然而,拥挤诱导的染色质紧缩的细节仍然知之甚少。在这项工作中,我们进行了一项计算机模拟研究,研究了大分子拥挤对称为核小体簇的染色质结构单元之间相互作用的熵效应。核小体簇通过由调和约束崩溃的核小体链来建模,该约束隐含地模拟了由组蛋白尾巴和连接组蛋白介导的核小体缔合。核小体簇的核小体密度被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簇之间的有效相互作用,结果发现,大分子拥挤程度的增加会引起高核小体密度的两个簇之间的吸引力相互作用。有趣的是,增加的大分子拥挤程度不会引起低核小体密度的两个簇之间的任何吸引力。我们的结果表明,大分子拥挤的熵效应可以增强异染色质中核小体簇之间的结合,但不能增强常染色质中核小体簇之间的结合,这是由于核小体包装程度的差异所致。