Silva Isabel T G, Fernandes Vinícius, Souza Caio, Treptow Werner, Santos Guilherme M
Laboratório de Farmacologia Molecular, Departamento de Farmácia, Universidade de Brasília, Brasília, Brazil.
Laboratório de Biologia Teórica e Computacional, Departamento de Biologia Celular, Universidade de Brasília, Brasília, Brazil.
J Lipid Res. 2017 May;58(5):934-940. doi: 10.1194/jlr.M074997. Epub 2017 Mar 22.
Changes in chromatin structure regulate gene expression and genome maintenance. Molecules that bind to the nucleosome, the complex of DNA and histone proteins, are key modulators of chromatin structure. Previous work indicated that cholesterol, a ubiquitous cellular lipid, may bind to chromatin in vivo, suggesting a potential function for lipids in modulating chromatin architecture. However, the molecular mechanisms of cholesterol's action on chromatin structure have remained unclear. Here, we explored the biophysical impact of cholesterol on nucleosome and chromatin fibers reconstituted in vitro and characterized in silico the cholesterol binding to the nucleosome. Our findings support that cholesterol assists 10 and 30 nm chromatin formation and induces folding of long chromatin fibers as a result of direct interaction of the cholesterol to six nucleosomal binding sites.
染色质结构的变化调节基因表达和基因组维持。与核小体(DNA和组蛋白的复合物)结合的分子是染色质结构的关键调节因子。先前的研究表明,胆固醇作为一种普遍存在的细胞脂质,可能在体内与染色质结合,这表明脂质在调节染色质结构方面具有潜在功能。然而,胆固醇对染色质结构作用的分子机制仍不清楚。在这里,我们探讨了胆固醇对体外重构的核小体和染色质纤维的生物物理影响,并通过计算机模拟对胆固醇与核小体的结合进行了表征。我们的研究结果支持,由于胆固醇与六个核小体结合位点的直接相互作用,胆固醇有助于10纳米和30纳米染色质的形成,并诱导长染色质纤维的折叠。