Laboratory of Cellular and Molecular Biomechanics, Department of Mammalian Regulatory Network, Graduate School of Biostudies, Kyoto University, Sakyo, Kyoto, Japan.
Laboratory of Biomechanics, Institute for Life and Medical Sciences, Kyoto University, Sakyo, Kyoto, Japan.
Commun Biol. 2024 Jan 23;7(1):83. doi: 10.1038/s42003-023-05750-w.
DNA underwinding (untwisting) is a crucial step in transcriptional activation. DNA underwinding occurs between the site where torque is generated by RNA polymerase (RNAP) and the site where the axial rotation of DNA is constrained. However, what constrains DNA axial rotation in the nucleus is yet unknown. Here, we show that the anchorage to the nuclear protein condensates constrains DNA axial rotation for DNA underwinding in the nucleolus. In situ super-resolution imaging of underwound DNA reveal that underwound DNA accumulates in the nucleolus, a nuclear condensate with a core-shell structure. Specifically, underwound DNA is distributed in the nucleolar core owing to RNA polymerase I (RNAPI) activities. Furthermore, underwound DNA in the core decreases when nucleolar shell components are prevented from binding to their recognition structure, G-quadruplex (G4). Taken together, these results suggest that the nucleolar shell provides anchoring sites that constrain DNA axial rotation for RNAPI-driven DNA underwinding in the core. Our findings will contribute to understanding how nuclear protein condensates make up constraints for the site-specific regulation of DNA underwinding and transcription.
DNA 超螺旋(解旋)是转录激活的关键步骤。DNA 超螺旋发生在由 RNA 聚合酶(RNAP)产生扭矩的部位和 DNA 轴向旋转受到限制的部位之间。然而,在核内限制 DNA 轴向旋转的因素尚不清楚。在这里,我们表明,锚定在核蛋白凝聚物上限制了核仁中 DNA 超螺旋的 DNA 轴向旋转。原位超分辨成像显示,超螺旋 DNA 积累在核仁中,核仁是一种具有核壳结构的核凝聚物。具体而言,由于 RNA 聚合酶 I(RNAPI)的活性,超螺旋 DNA 分布在核仁核心中。此外,当核仁壳成分被阻止与其识别结构 G-四链体(G4)结合时,核心中的超螺旋 DNA 减少。总之,这些结果表明核仁壳提供了锚定点,限制了由 RNAPI 驱动的 DNA 超螺旋和转录中的 DNA 轴向旋转。我们的发现将有助于理解核蛋白凝聚物如何构成 DNA 超螺旋和转录的特定部位调节的限制。