Chujo Takeshi, Yamazaki Tomohiro, Kawaguchi Tetsuya, Kurosaka Satoshi, Takumi Toru, Nakagawa Shinichi, Hirose Tetsuro
Institute for Genetic Medicine, Hokkaido University, Sapporo Hokkaido, Japan.
Brain Science Institute, RIKEN, Wako Saitama, Japan.
EMBO J. 2017 May 15;36(10):1447-1462. doi: 10.15252/embj.201695848. Epub 2017 Apr 12.
long noncoding RNA (lncRNA) is the molecular scaffold of paraspeckle nuclear bodies. Here, we report an improved RNA extraction method: extensive needle shearing or heating of cell lysate in RNA extraction reagent improved extraction by 20-fold (a property we term "semi-extractability"), whereas using a conventional method was trapped in the protein phase. The improved extraction method enabled us to estimate that approximately 50 molecules are present in a single paraspeckle. Another architectural lncRNA, , also exhibited similar semi-extractability. A comparison of RNA-seq data from needle-sheared and control samples revealed the existence of multiple semi-extractable RNAs, many of which were localized in subnuclear granule-like structures. The semi-extractability of correlated with its association with paraspeckle proteins and required the prion-like domain of the RNA-binding protein FUS This observation suggests that tenacious RNA-protein and protein-protein interactions, which drive nuclear body formation, are responsible for semi-extractability. Our findings provide a foundation for the discovery of the architectural RNAs that constitute nuclear bodies.
长链非编码RNA(lncRNA)是旁斑核小体的分子支架。在此,我们报告一种改进的RNA提取方法:在RNA提取试剂中对细胞裂解物进行广泛的针剪或加热,可使提取效率提高20倍(我们将此特性称为“半可提取性”),而使用传统方法时RNA被困在蛋白质相中。改进的提取方法使我们能够估计单个旁斑中大约存在50个分子。另一种结构性lncRNA也表现出类似的半可提取性。对针剪样本和对照样本的RNA测序数据进行比较,揭示了多种半可提取RNA的存在,其中许多定位于亚核颗粒样结构中。的半可提取性与其与旁斑蛋白的结合相关,并且需要RNA结合蛋白FUS的朊病毒样结构域。这一观察结果表明,驱动核小体形成的紧密RNA-蛋白质和蛋白质-蛋白质相互作用是半可提取性的原因。我们的发现为发现构成核小体的结构性RNA奠定了基础。