Beijing National Laboratory for Molecular Sciences (BNLMS), State Key Laboratory for Structural Chemistry of Unstable and Stable Species, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China.
Peking-Tsinghua Center for Life Sciences, Peking University, Beijing 100871, China.
Int J Mol Sci. 2022 Apr 21;23(9):4594. doi: 10.3390/ijms23094594.
Biomacromolecules often form condensates to function in cells. VRN1 is a transcriptional repressor that plays a key role in plant vernalization. Containing two DNA-binding domains connected by an intrinsically disordered linker (IDL), VRN1 was shown to undergo liquid-like phase separation with DNA, and the length and charge pattern of IDL play major regulatory roles. However, the underlying mechanism remains elusive. Using a polymer chain model and lattice-based Monte-Carlo simulations, we comprehensively investigated how the IDL regulates VRN1 and DNA phase separation. Using a worm-like chain model, we showed that the IDL controls the binding affinity of VRN1 to DNA, by modulating the effective local concentration of the VRN1 DNA-binding domains. The predicted binding affinities, under different IDL lengths, were in good agreement with previously reported experimental results. Our simulation of the phase diagrams of the VRN1 variants with neutral IDLs and DNA revealed that the ability of phase separation first increased and then decreased, along with the increase in the linker length. The strongest phase separation ability was achieved when the linker length was between 40 and 80 residues long. Adding charged patches to the IDL resulted in robust phase separation that changed little with IDL length variations. Our study provides mechanism insights on how IDL regulates VRN1 and DNA phase separation, and why naturally occurring VRN1-like proteins evolve to contain the charge segregated IDL sequences, which may also shed light on the molecular mechanisms of other IDL-regulated phase separation processes in living cells.
生物大分子经常形成凝聚物以在细胞中发挥功能。VRN1 是一种转录抑制剂,在植物春化中起着关键作用。VRN1 包含两个通过固有无序连接体 (IDL) 连接的 DNA 结合结构域,被证明与 DNA 发生类似液体的相分离,并且 IDL 的长度和电荷模式起着主要的调节作用。然而,其潜在的机制仍然难以捉摸。使用聚合物链模型和基于晶格的蒙特卡罗模拟,我们全面研究了 IDL 如何调节 VRN1 和 DNA 相分离。使用蠕虫状链模型,我们表明 IDL 通过调节 VRN1 DNA 结合结构域的有效局部浓度来控制 VRN1 与 DNA 的结合亲和力。在不同 IDL 长度下预测的结合亲和力与之前报道的实验结果非常吻合。我们对中性 IDL 和 DNA 的 VRN1 变体的相图进行了模拟,结果表明,随着连接体长度的增加,相分离的能力先增加后减少。当连接体长度在 40 到 80 个残基之间时,相分离能力最强。在 IDL 中添加带电荷的补丁会导致强烈的相分离,其变化与 IDL 长度变化几乎没有关系。我们的研究提供了关于 IDL 如何调节 VRN1 和 DNA 相分离以及为什么天然存在的 VRN1 样蛋白进化为包含电荷分离 IDL 序列的机制见解,这也可能为活细胞中其他 IDL 调节的相分离过程的分子机制提供启示。