{"title":"Polymer Collapse and Liquid-Liquid Phase-Separation are Coupled in a Generalized Prewetting Transition","authors":"Mason N. Rouches, Benjamin B. Machta","doi":"arxiv-2404.19158","DOIUrl":null,"url":null,"abstract":"The three-dimensional organization of chromatin is thought to play an\nimportant role in controlling gene expression. Specificity in expression is\nachieved through the interaction of transcription factors and other nuclear\nproteins with particular sequences of DNA. At unphysiological concentrations\nmany of these nuclear proteins can phase-separate in the absence of DNA, and it\nhas been hypothesized that, in vivo, the thermodynamic forces driving these\nphases help determine chromosomal organization. However it is unclear how DNA,\nitself a long polymer subject to configurational transitions, interacts with\nthree-dimensional protein phases. Here we show that a long compressible polymer\ncan be coupled to interacting protein mixtures, leading to a generalized\nprewetting transition where polymer collapse is coincident with a locally\nstabilized liquid droplet. We use lattice Monte-Carlo simulations and a\nmean-field theory to show that these phases can be stable even in regimes where\nboth polymer collapse and coexisting liquid phases are unstable in isolation,\nand that these new transitions can be either abrupt or continuous. For polymers\nwith internal linear structure we further show that changes in the\nconcentration of bulk components can lead to changes in three-dimensional\npolymer structure. In the nucleus there are many distinct proteins that\ninteract with many different regions of chromatin, potentially giving rise to\nmany different Prewet phases. The simple systems we consider here highlight\nchromatin's role as a lower-dimensional surface whose interactions with\nproteins are required for these novel phases.","PeriodicalId":501170,"journal":{"name":"arXiv - QuanBio - Subcellular Processes","volume":"15 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Subcellular Processes","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2404.19158","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The three-dimensional organization of chromatin is thought to play an
important role in controlling gene expression. Specificity in expression is
achieved through the interaction of transcription factors and other nuclear
proteins with particular sequences of DNA. At unphysiological concentrations
many of these nuclear proteins can phase-separate in the absence of DNA, and it
has been hypothesized that, in vivo, the thermodynamic forces driving these
phases help determine chromosomal organization. However it is unclear how DNA,
itself a long polymer subject to configurational transitions, interacts with
three-dimensional protein phases. Here we show that a long compressible polymer
can be coupled to interacting protein mixtures, leading to a generalized
prewetting transition where polymer collapse is coincident with a locally
stabilized liquid droplet. We use lattice Monte-Carlo simulations and a
mean-field theory to show that these phases can be stable even in regimes where
both polymer collapse and coexisting liquid phases are unstable in isolation,
and that these new transitions can be either abrupt or continuous. For polymers
with internal linear structure we further show that changes in the
concentration of bulk components can lead to changes in three-dimensional
polymer structure. In the nucleus there are many distinct proteins that
interact with many different regions of chromatin, potentially giving rise to
many different Prewet phases. The simple systems we consider here highlight
chromatin's role as a lower-dimensional surface whose interactions with
proteins are required for these novel phases.
染色质的三维组织被认为在控制基因表达方面发挥着重要作用。基因表达的特异性是通过转录因子和其他核蛋白与 DNA 的特定序列相互作用来实现的。据推测,在体内,驱动这些相位的热动力有助于决定染色体的组织结构。然而,DNA本身是一种长聚合物,会发生构型转换,目前还不清楚DNA如何与三维蛋白质相相互作用。在这里,我们展示了一种可压缩的长聚合物可以与相互作用的蛋白质混合物耦合,从而导致一种广义的润湿转变,在这种转变中,聚合物的塌缩与局部稳定的液滴相吻合。我们利用晶格蒙特卡洛模拟和均场理论证明,即使在聚合物塌缩和共存液相单独存在时都不稳定的情况下,这些相位也能保持稳定,而且这些新的转变可以是突然的,也可以是连续的。对于具有内部线性结构的聚合物,我们进一步表明,主体成分浓度的变化会导致三维聚合物结构的变化。在细胞核中,有许多不同的蛋白质与染色质的许多不同区域发生相互作用,从而可能产生许多不同的预湿阶段。我们在此考虑的简单系统突出了染色质作为低维表面的作用,它与蛋白质的相互作用是这些新阶段所必需的。