Promoter G-quadruplexes and transcription factors cooperate to shape the cell type-specific transcriptome

被引:122
|
作者
Lago, Sara [1 ]
Nadai, Matteo [1 ]
Cernilogar, Filippo M. [2 ]
Kazerani, Maryam [2 ]
Moreno, Helena Dominiguez [2 ]
Schotta, Gunnar [2 ]
Richter, Sara N. [1 ]
机构
[1] Univ Padua, Dept Mol Med, Padua, Italy
[2] Ludwig Maximilians Univ Munchen, Fac Med, Biomed Ctr, Div Mol Biol, Martinsried, Germany
基金
欧洲研究理事会;
关键词
IN-VIVO; SEQUENCE MOTIFS; GENE-EXPRESSION; SMALL-MOLECULE; FACTOR SP1; DNA; VISUALIZATION; BINDING; CANCER; IDENTIFICATION;
D O I
10.1038/s41467-021-24198-2
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
Cell identity is maintained by activation of cell-specific gene programs, regulated by epigenetic marks, transcription factors and chromatin organization. DNA G-quadruplex (G4)-folded regions in cells were reported to be associated with either increased or decreased transcriptional activity. By G4-ChIP-seq/RNA-seq analysis on liposarcoma cells we confirmed that G4s in promoters are invariably associated with high transcription levels in open chromatin. Comparing G4 presence, location and transcript levels in liposarcoma cells to available data on keratinocytes, we showed that the same promoter sequences of the same genes in the two cell lines had different G4-folding state: high transcript levels consistently associated with G4-folding. Transcription factors AP-1 and SP1, whose binding sites were the most significantly represented in G4-folded sequences, coimmunoprecipitated with their G4-folded promoters. Thus, G4s and their associated transcription factors cooperate to determine cell-specific transcriptional programs, making G4s to strongly emerge as new epigenetic regulators of the transcription machinery. G-quadruplex (G4) structures play complex roles linked to transcription regulation. Here the authors, by comparing G4 location and transcript levels in liposarcoma and keratinocyte cells, reveal that G4s cooperate with transcription factors to determine cell-specific transcriptional programs.
引用
收藏
页数:13
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