Centro de Biología Molecular Severo Ochoa, CSIC-UAM, CL Nicolás Cabrera, 1, 28049 Madrid, Spain.
Centro de Biología Molecular Severo Ochoa, CSIC-UAM, CL Nicolás Cabrera, 1, 28049 Madrid, Spain.
Int J Biol Macromol. 2024 Sep;276(Pt 1):133822. doi: 10.1016/j.ijbiomac.2024.133822. Epub 2024 Jul 14.
DNA loop extrusion plays a key role in the regulation of gene expression and the structural arrangement of chromatin. Most existing mechanistic models of loop extrusion depend on some type of ratchet mechanism, which should permit the elongation of loops while preventing their collapse, by enabling DNA to move in only one direction. STAG2 is already known to exert a role as DNA anchor, but the available structural data suggest a possible role in unidirectional DNA motion. In this work, a computational simulation framework was constructed to evaluate whether STAG2 could enforce such unidirectional displacement of a DNA double helix. The results reveal that STAG2 V-shape allows DNA sliding in one direction, but blocks opposite DNA movement via a linear ratchet mechanism. Furthermore, these results suggest that RAD21 binding to STAG2 controls its flexibility by narrowing the opening of its V-shape, which otherwise remains widely open in absence of RAD21. Therefore, in the proposed model, in addition to its already described role as a DNA anchor, the STAG2-RAD21 complex would be part of a ratchet mechanism capable of exerting directional selectivity on DNA sliding during loop extrusion. The identification of the molecular basis of the ratchet mechanism of loop extrusion is a critical step in unraveling new insights into a broad spectrum of chromatin activities and their implications for the mechanisms of chromatin-related diseases.
DNA 环挤出在基因表达调控和染色质结构排列中起着关键作用。大多数现有的环挤出机制模型都依赖于某种棘轮机制,这种机制应该允许环的延伸,同时防止它们的崩溃,从而使 DNA 只能朝一个方向移动。STAG2 已经被证明在 DNA 锚定中发挥作用,但现有的结构数据表明它可能在单向 DNA 运动中发挥作用。在这项工作中,构建了一个计算模拟框架来评估 STAG2 是否能够强制 DNA 双链朝一个方向移动。结果表明,STAG2 的 V 形结构允许 DNA 朝一个方向滑动,但通过线性棘轮机制阻止相反的 DNA 运动。此外,这些结果表明,RAD21 与 STAG2 的结合通过缩小其 V 形结构的开口来控制其灵活性,否则在没有 RAD21 的情况下,其开口会保持很大。因此,在提出的模型中,除了其已经描述的 DNA 锚定作用外,STAG2-RAD21 复合物将成为一种棘轮机制的一部分,该机制能够在环挤出过程中对 DNA 滑动施加方向选择性。确定环挤出棘轮机制的分子基础是揭示广泛的染色质活性及其对染色质相关疾病机制的新见解的关键步骤。