Falkenberg Cibele Vieira, Carson John H, Blinov Michael L
Mechanical Engineering Department, Samuel Ginn College of Engineering, Auburn University, Auburn, Alabama.
Center for Cell Analysis and Modeling, University of Connecticut School of Medicine, Farmington, Connecticut; Department of Molecular Biology and Biophysics, University of Connecticut School of Medicine, Farmington, Connecticut.
Biophys J. 2017 Jul 25;113(2):235-245. doi: 10.1016/j.bpj.2017.01.031. Epub 2017 Feb 24.
RNA granules are ensembles of specific RNA and protein molecules that mediate localized translation in eukaryotic cells. The mechanisms for formation and selectivity of RNA granules are unknown. Here we present a model for assembly of one type of RNA granule based on experimentally measured binding interactions among three core multivalent molecular components necessary for such assembly: specific RNA molecules that contain a cis-acting sequence called the A2 response element (A2RE), hnRNP A2 proteins that bind specifically (with high affinity) to A2RE sequences or nonspecifically (with lower affinity) to other RNA sequences, and heptavalent protein cytoskeleton-associated protein 5 (CKAP5, an alternative name for TOG protein) that binds both hnRNP A2 molecules and RNA. Non-A2RE RNA molecules (RNA without the A2RE sequence) that may be recruited to the granules through nonspecific interactions are also considered in the model. Modeling multivalent molecular interactions in granules is challenging because of combinatorial complexity in the number of potential molecular complexes among these core components and dynamic changes in granule composition and structure in response to changes in local intracellular environment. We use a hybrid modeling approach (deterministic-stochastic-statistical) that is appropriate when the overall compositions of multimolecular ensembles are of greater importance than the specific interactions among individual molecular components. Modeling studies titrating the concentrations of various granule components and varying effective site pair affinities and RNA valency demonstrate that interactions between multivalent components (TOG and RNA) are modulated by a bivalent adaptor molecule (hnRNP A2). Formation and disruption of granules, as well as RNA selectivity in granule composition are regulated by distinct concentration regimes of A2. Our results suggest that granule assembly is tightly controlled by multivalent molecular interactions among RNA molecules, adaptor proteins, and scaffold proteins.
RNA颗粒是特定RNA和蛋白质分子的集合体,介导真核细胞中的局部翻译。RNA颗粒的形成和选择性机制尚不清楚。在此,我们基于对组装所需的三种核心多价分子成分之间实验测量的结合相互作用,提出了一种RNA颗粒组装模型:包含称为A2反应元件(A2RE)的顺式作用序列的特定RNA分子、与A2RE序列特异性(高亲和力)结合或与其他RNA序列非特异性(低亲和力)结合的hnRNP A2蛋白,以及与hnRNP A2分子和RNA都结合的七价蛋白细胞骨架相关蛋白5(CKAP5,TOG蛋白的另一个名称)。该模型还考虑了可能通过非特异性相互作用被招募到颗粒中的非A2RE RNA分子(没有A2RE序列的RNA)。由于这些核心成分之间潜在分子复合物数量的组合复杂性以及颗粒组成和结构响应局部细胞内环境变化的动态变化,对颗粒中的多价分子相互作用进行建模具有挑战性。我们使用一种混合建模方法(确定性 - 随机 - 统计),当多分子集合体的整体组成比单个分子成分之间的特定相互作用更重要时,这种方法是合适的。对各种颗粒成分浓度进行滴定以及改变有效位点对亲和力和RNA价态的建模研究表明,多价成分(TOG和RNA)之间的相互作用由二价衔接分子(hnRNP A2)调节。颗粒的形成和破坏以及颗粒组成中的RNA选择性受A2不同浓度范围的调节。我们的结果表明,颗粒组装受到RNA分子、衔接蛋白和支架蛋白之间多价分子相互作用的严格控制。