R-loop induced G-quadruplex in non-template promotes transcription by successive R-loop formation

被引:70
|
作者
Lee, Chun-Ying [1 ]
McNerney, Christina [2 ]
Ma, Kevin [1 ]
Zhao, Walter [3 ]
Wang, Ashley [1 ]
Myong, Sua [1 ,4 ]
机构
[1] Johns Hopkins Univ, Dept Biophys, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Dept Biol, Baltimore, MD 21218 USA
[3] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD 21218 USA
[4] Univ Illinois, Ctr Phys Living Cells, Phys Frontier Ctr, Urbana, IL 61801 USA
基金
美国国家科学基金会;
关键词
INDUCED FLUORESCENCE ENHANCEMENT; RNA-POLYMERASE; DNA; GENE; MOLECULE; BLOCKAGE; SEQUENCE; MECHANISMS; REGION; PIFE;
D O I
10.1038/s41467-020-17176-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
G-quadruplex (G4) is a noncanonical secondary structure of DNA or RNA which can enhance or repress gene expression, yet the underlying molecular mechanism remains uncertain. Here we show that when positioned downstream of transcription start site, the orientation of potential G4 forming sequence (PQS), but not the sequence alters transcriptional output. Ensemble in vitro transcription assays indicate that PQS in the non-template increases mRNA production rate and yield. Using sequential single molecule detection stages, we demonstrate that while binding and initiation of T7 RNA polymerase is unchanged, the efficiency of elongation and the final mRNA output is higher when PQS is in the non-template. Strikingly, the enhanced elongation arises from the transcription-induced R-loop formation, which in turn generates G4 structure in the non-template. The G4 stabilized R-loop leads to increased transcription by a mechanism involving successive rounds of R-loop formation.
引用
收藏
页数:15
相关论文
共 50 条
  • [1] R-loop induced G-quadruplex in non-template promotes transcription by successive R-loop formation
    Chun-Ying Lee
    Christina McNerney
    Kevin Ma
    Walter Zhao
    Ashley Wang
    Sua Myong
    Nature Communications, 11
  • [2] Interference of PNA binding to the non-template strand with transcription supports the general model for transcription blockage by R-loop formation
    Belotserkovskii, Boris P.
    Hanawalt, Philip C.
    JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 2015, 33 : 14 - 14
  • [3] PNA binding to the non-template DNA strand interferes with transcription, suggesting a blockage mechanism mediated by R-loop formation
    Belotserkovskii, Boris P.
    Hanawalt, Philip C.
    MOLECULAR CARCINOGENESIS, 2015, 54 (11) : 1508 - 1512
  • [4] Single-molecule fluorescence studies on cotranscriptional G-quadruplex formation coupled with R-loop formation
    Lim, Gunhyoung
    Hohng, Sungchul
    NUCLEIC ACIDS RESEARCH, 2020, 48 (16) : 9195 - 9203
  • [5] Programmed R-loop formation
    Linda Koch
    Nature Reviews Genetics, 2016, 17 (8) : 438 - 438
  • [6] TET Deficiency Is Associated with Accumulation of G-Quadruplex and R-Loop Structures during Oncogenesis
    Shukla, Vipul
    Samaniego-Castruita, Daniela
    Dong, Zhen
    Avalos, Edahi Gonzalez
    Yan, Qingqing
    Sarma, Kavitha
    Rao, Anjana
    BLOOD, 2021, 138
  • [7] The problem of hypernegative supercoiling and R-loop formation in transcription
    Drolet, M
    Broccoli, S
    Rallu, F
    Hraiky, C
    Fortin, C
    Massé, É
    Baaklini, I
    FRONTIERS IN BIOSCIENCE, 2003, 8 : D210 - D221
  • [8] m6A promotes R-loop formation to facilitate transcription termination
    Yang, Xin
    Liu, Qian-Lan
    Xu, Wei
    Zhang, Yi-Chang
    Yang, Ying
    Ju, Lin-Fang
    Chen, Jing
    Chen, Yu-Sheng
    Li, Kuan
    Ren, Jie
    Sun, Qianwen
    Yang, Yun-Gui
    CELL RESEARCH, 2019, 29 (12) : 1035 - 1038
  • [9] m6A promotes R-loop formation to facilitate transcription termination
    Xin Yang
    Qian-Lan Liu
    Wei Xu
    Yi-Chang Zhang
    Ying Yang
    Lin-Fang Ju
    Jing Chen
    Yu-Sheng Chen
    Kuan Li
    Jie Ren
    Qianwen Sun
    Yun-Gui Yang
    Cell Research, 2019, 29 : 1035 - 1038
  • [10] Helicases in R-loop Formation and Resolution
    Yang, Shizhuo
    Winstone, Lacey
    Mondal, Sohaumn
    Wu, Yuliang
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2023, 299 (11)