Evidence map›Paper›PMID 34400476›Full record

ArticleGenome research2021

Ligand-induced native G-quadruplex stabilization impairs transcription initiation.

Conghui Li, Honghong Wang, Zhinang Yin, Pingping Fang, Ruijing Xiao, Ying Xiang, Wen Wang, Qiuzi Li, Beili Huang, Jian Huang and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

70 citing papers in PubMed, 129 citations in OpenAlex.

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10 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Conghui Li *Department of Pathophysiology, School of Basic Medical Sciences, Wuhan University, Wuhan 430071, China.ORCID 0000-0002-4991-4474
Honghong Wang *Department of Pathophysiology, School of Basic Medical Sciences, Wuhan University, Wuhan 430071, China.ORCID 0000-0002-3485-9046
Zhinang Yin *Department of Pathophysiology, School of Basic Medical Sciences, Wuhan University, Wuhan 430071, China.ORCID 0000-0002-1275-3929
Pingping Fang *Department of Pharmacology, School of Basic Medical Sciences, Wuhan University, Wuhan 430071, China.ORCID 0000-0001-5305-2830
Ruijing XiaoDepartment of Pathophysiology, School of Basic Medical Sciences, Wuhan University, Wuhan 430071, China.ORCID 0000-0002-5753-6557
Ying XiangDepartment of Pathophysiology, School of Basic Medical Sciences, Wuhan University, Wuhan 430071, China.ORCID 0000-0001-9165-3346
Wen WangDepartment of Pathophysiology, School of Basic Medical Sciences, Wuhan University, Wuhan 430071, China.ORCID 0000-0002-7413-5368
Qiuzi LiCollege of Life Sciences, Wuhan University, Wuhan 430071, China.ORCID 0000-0001-8671-1249
Beili HuangDepartment of Pathophysiology, School of Basic Medical Sciences, Wuhan University, Wuhan 430071, China.ORCID 0000-0001-6989-1671
Jian HuangCollege of Life Sciences, Wuhan University, Wuhan 430071, China.ORCID 0000-0003-2094-5055
Kaiwei LiangDepartment of Pathophysiology, School of Basic Medical Sciences, Wuhan University, Wuhan 430071, China.ORCID 0000-0002-6021-353X
Wuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G-quadruplexes (G4s) are noncanonical DNA secondary structures formed through the self-association of guanines, and G4s are distributed widely across the genome. G4 participates in multiple biological processes including gene transcription, and G4-targeted ligands serve as potential therapeutic agents for DNA-targeted therapies. However, genome-wide studies of the exact roles of G4s in transcriptional regulation are still lacking. Here, we establish a sensitive G4-CUT&Tag method for genome-wide profiling of native G4s with high resolution and specificity. We find that native G4 signals are cell type-specific and are associated with transcriptional regulatory elements carrying active epigenetic modifications. Drug-induced promoter-proximal RNA polymerase II pausing promotes nearby G4 formation. In contrast, G4 stabilization by G4-targeted ligands globally reduces RNA polymerase II occupancy at gene promoters as well as nascent RNA synthesis. Moreover, ligand-induced G4 stabilization modulates chromatin states and impedes transcription initiation via inhibition of general transcription factors loading to promoters. Together, our study reveals a reciprocal genome-wide regulation between native G4 dynamics and gene transcription, which will deepen our understanding of G4 biology toward therapeutically targeting G4s in human diseases.

Indexed as

G-QuadruplexesTranscription Initiation, GeneticChromatinDNALigandsPromoter Regions, GeneticChromatinDNALigands

Identifiers

PMID34400476
PMCPMC8415369
OpenAlexW3194657369

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.