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同时探测转录、G-四联体和 R 环。

Simultaneous probing of transcription, G-quadruplex, and R-loop.

机构信息

Program in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.

Program in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.

出版信息

Methods Enzymol. 2024;705:377-396. doi: 10.1016/bs.mie.2024.07.004. Epub 2024 Aug 9.

Abstract

DNA and RNA can form various non-canonical secondary structures, including G-quadruplex (G4) and R-loops. These structures are considered transcriptional regulatory elements due to their enrichment at regulatory regions. During transcription, G-rich sequences in the non-template strand promote R-loop formation in the DNA template strand. These R-loops induce G4 structures in the non-template DNA strand, further stabilizing them. Additionally, the high rG: dC base-pairing within the R-loop contributes to the stability of DNA/RNA hybridization. Our previous study investigated the interplay between G4s and R-loops and its impact on transcription. We employed two techniques to demonstrate transcription-mediated G4 and R-loop formation. The single-molecule method allows us to detect intricate details of transcription initiation, elongation, and co-transcriptional R-loop and G4 formation. It provides a high-resolution view of the dynamic processes involved in transcriptional regulation. As an orthogonal approach, a gel-based assay enables the detection of the transcription-mediated R-loops and the RNA product. We can measure the progressive formation of R-loop and total RNA produced from transcription by analyzing gel electrophoresis patterns. In summary, these techniques provide valuable insights into the non-canonical nucleic acid structures and their impact on gene expression.

摘要

DNA 和 RNA 可以形成各种非规范的二级结构,包括 G-四联体 (G4) 和 R 环。由于它们在调控区域的富集,这些结构被认为是转录调控元件。在转录过程中,非模板链上富含 G 的序列促进 DNA 模板链上 R 环的形成。这些 R 环在非模板 DNA 链上诱导 G4 结构,进一步稳定它们。此外,R 环内的高 rG:dC 碱基配对有助于 DNA/RNA 杂交的稳定性。我们之前的研究探讨了 G4 和 R 环之间的相互作用及其对转录的影响。我们采用了两种技术来证明转录介导的 G4 和 R 环的形成。单分子方法使我们能够检测转录起始、延伸和共转录 R 环和 G4 形成的复杂细节。它提供了转录调控中涉及的动态过程的高分辨率视图。作为一种正交方法,基于凝胶的测定法可用于检测转录介导的 R 环和 RNA 产物。通过分析凝胶电泳模式,我们可以测量 R 环和转录产生的总 RNA 的渐进形成。总之,这些技术为非规范核酸结构及其对基因表达的影响提供了有价值的见解。

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