DNA supercoiling-mediated G4/R-loop formation tunes transcription by controlling the access of RNA polymerase

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作者
Jihee Hwang [1 ]
Chun-Ying Lee [1 ]
Sumitabha Brahmachari [2 ]
Shubham Tripathi [3 ]
Tapas Paul [1 ]
Huijin Lee [4 ]
Alanna Craig [5 ]
Taekjip Ha [1 ]
Sua Myong [4 ]
机构
[1] Boston Children’s Hospital and Harvard Medical School,Programs in Cellular and Molecular Medicine
[2] Rice University,Center for Theoretical Biological Physics
[3] Yale School of Medicine,Yale Center for Systems and Engineering Immunology & Department of Immunobiology
[4] Johns Hopkins University School of Medicine,Department of Biophysics and Biophysical Chemistry
[5] Johns Hopkins University,Biophysics
[6] Johns Hopkins University,Program in Cellular Molecular Developmental Biology
[7] Johns Hopkins University,Howard Hughes Medical Institute
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D O I
10.1038/s41467-025-58479-x
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摘要
RNA polymerase (RNAP) is a processive motor that modulates DNA supercoiling and reshapes DNA structures. The feedback loop between the DNA topology and transcription remains elusive. Here, we investigate the impact of potential G-quadruplex forming sequences (PQS) on transcription in response to DNA supercoiling. We find that supercoiled DNA increases transcription frequency 10-fold higher than relaxed DNA, which lead to an abrupt formation of G-quadruplex (G4) and R-loop structures. Moreover, the stable R-loop relieves topological strain, facilitated by G4 formation. The cooperative formation of G4/R-loop effectively alters the DNA topology around the promoter and suppresses transcriptional activity by impeding RNAP loading. These findings highlight negative supercoiling as a built-in spring that triggers a transcriptional burst followed by a rapid suppression upon G4/R-loop formation. This study sheds light on the intricate interplay between DNA topology and structural change in transcriptional regulation, with implications for understanding gene expression dynamics.
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