Cancer Research UK Cambridge Institute, Li Ka Shing Centre, Robinson Way, Cambridge CB2 0RE, UK.
Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, UK.
Nat Chem. 2014 Jan;6(1):75-80. doi: 10.1038/nchem.1805. Epub 2013 Nov 24.
Following extensive evidence for the formation of four-stranded DNA G-quadruplex structures in vitro, DNA G-quadruplexes have been observed within human cells. Although chemically distinct, RNA can also fold in vitro into G-quadruplex structures that are highly stable because of the 2'-hydroxyl group. However, RNA G-quadruplexes have not yet been reported in cells. Here, we demonstrate the visualization of RNA G-quadruplex structures within the cytoplasm of human cells using a G-quadruplex structure-specific antibody. We also demonstrate that small molecules that bind to G-quadruplexes in vitro can trap endogenous RNA G-quadruplexes when applied to cells. Furthermore, a small molecule that exhibits a preference for RNA G-quadruplexes rather than DNA G-quadruplexes in biophysical experiments also shows the same selectivity within a cellular context. Our findings provide substantive evidence for RNA G-quadruplex formation in the human transcriptome, and corroborate the selectivity and application of stabilizing ligands that target G-quadruplexes within a cellular context.
在体外形成四链 DNA G-四链体结构的大量证据之后,已经在人类细胞内观察到 DNA G-四链体。尽管在化学上有所不同,但 RNA 也可以在体外折叠成高度稳定的 G-四链体结构,这是由于 2'-羟基。然而,RNA G-四链体尚未在细胞中报道。在这里,我们使用 G-四链体结构特异性抗体证明了人细胞细胞质中 RNA G-四链体结构的可视化。我们还证明,当应用于细胞时,在体外与 G-四链体结合的小分子可以捕获内源性 RNA G-四链体。此外,在生物物理实验中表现出对 RNA G-四链体而不是 DNA G-四链体偏好的小分子在细胞环境中也表现出相同的选择性。我们的发现为人类转录组中 RNA G-四链体的形成提供了实质性证据,并证实了在细胞环境中靶向 G-四链体的稳定配体的选择性和应用。