Mathematical model of structural changes in nuclear speckle.

Biophysics and Physicobiology Pub Date : 2023-04-27 eCollection Date: 2023-01-01 DOI:10.2142/biophysico.bppb-v20.0020
Shingo Wakao, Noriko Saitoh, Akinori Awazu
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Abstract

Nuclear speckles are nuclear bodies consisting of populations of small and irregularly shaped droplet-like molecular condensates that contain various splicing factors. Recent experiments have revealed the following structural features of nuclear speckles: (I) Each molecular condensate contains SON and SRRM2 proteins, and MALAT1 non-coding RNA surrounds these condensates; (II) During normal interphase of the cell cycle in multicellular organisms, these condensates are broadly distributed throughout the nucleus. In contrast, when cell transcription is suppressed, the condensates fuse and form strongly condensed spherical droplets; (III) SON is dispersed spatially in MALAT1 knocked-down cells and MALAT1 is dispersed in SON knocked-down cells because of the collapse of the nuclear speckles. However, the detailed interactions among the molecules that are mechanistically responsible for the structural variation remain unknown. In this study, a coarse-grained molecular dynamics model of the nuclear speckle was developed by considering the dynamics of SON, SRRM2, MALAT1, and pre-mRNA as representative components of the condensates. The simulations reproduced the structural changes, which were used to predict the interaction network among the representative components of the condensates.

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核斑点结构变化的数学模型。
核斑点是由形状不规则的小液滴状分子凝聚体组成的核体,其中含有各种剪接因子。最近的实验揭示了核斑点的以下结构特征:(I)每个分子凝聚体都含有 SON 和 SRRM2 蛋白,MALAT1 非编码 RNA 环绕在这些凝聚体周围;(II)在多细胞生物细胞周期的正常间期,这些凝聚体广泛分布在整个细胞核中。相反,当细胞转录受到抑制时,凝聚体融合并形成强烈凝聚的球形液滴;(III) 在 MALAT1 基因敲除的细胞中,SON 在空间上是分散的,而在 SON 基因敲除的细胞中,MALAT1 是分散的,因为核斑点塌陷了。然而,从机理上导致结构变化的分子间相互作用的细节仍然未知。在本研究中,通过考虑 SON、SRRM2、MALAT1 和 pre-mRNA 作为凝集物代表性成分的动力学,建立了核斑点的粗粒度分子动力学模型。模拟再现了结构的变化,并以此预测凝集物代表性成分之间的相互作用网络。
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