State Key Laboratory of Biomembrane and Membrane Biotechnology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101 (P. R. China).
Key Laboratory of Zebrafish Modeling and Drug Screening for Human Diseases of Guangdong Higher Education Institutes, Department of Cell Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515 (P. R. China).
Angew Chem Int Ed Engl. 2015 Jul 27;54(31):8992-6. doi: 10.1002/anie.201503648. Epub 2015 Jun 12.
G-quadruplex-forming sequences are enriched near transcription start sites (TSSs) in animal genes. They readily form G-quadruplexes in transcription, which in turn regulate transcription. Therefore, the control of G-quadruplex formation is important for their functionality. It is now shown that G-quadruplexes form efficiently on the non-template, but hardly on the template DNA strand in the downstream vicinity of TSSs in DNA duplexes when they are transcribed by the T7 RNA polymerase (RNAP). Structural analysis reveals that the T7 RNAP causes distortion in a DNA duplex both inside and in front of the enzyme. This structural distortion leads to strand-biased G-quadruplex formation when a G-quadruplex-forming sequence is partially fed into the T7 RNAP to a position about seven nucleotides away from the front of RNA synthesis. Based on these facts, we propose a model for the strand-biased formation of G-quadruplexes in transcribed DNA duplexes.
富含四链体形成序列的动物基因在转录起始位点(TSS)附近。它们在转录过程中很容易形成四链体,从而调节转录。因此,控制四链体的形成对于其功能非常重要。现在已经表明,当 T7 RNA 聚合酶(RNAP)转录 DNA 双链体中的 TSS 下游附近的非模板链时,四链体可以有效地形成,但模板链上几乎没有形成。结构分析表明,T7 RNAP 在酶的内部和前面使 DNA 双链体扭曲。当四链体形成序列部分进入 T7 RNAP 到距 RNA 合成前端约七个核苷酸的位置时,这种结构扭曲导致链偏向的四链体形成。基于这些事实,我们提出了一个模型,用于解释在转录的 DNA 双链体中链偏向的四链体形成。