Evidence map›Paper›PMID 27471032›Full record

ArticleNucleic acids research2016

G-quadruplex and G-rich sequence stimulate Pif1p-catalyzed downstream duplex DNA unwinding through reducing waiting time at ss/dsDNA junction.

Bo Zhang, Wen-Qiang Wu, Na-Nv Liu, Xiao-Lei Duan, Ming Li, Shuo-Xing Dou, Xi-Miao Hou, Xu-Guang Xi

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-weighted citation impact, top 21% of its field
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

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. DNA-unwinding activity ofThe Journal of biological chemistry · 2018
    Article
  12. Article
  13. Article
  14. Structure and function of Pif1 helicase.Biochemical Society transactions · 2017
    Review
  15. Article
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

8 authors at 2 institutions in 2 countries.

Bo ZhangCollege of Life Sciences, Northwest A&F University, Yangling, Shaanxi 712100, China.
Wen-Qiang WuCollege of Life Sciences, Northwest A&F University, Yangling, Shaanxi 712100, China.
Na-Nv LiuCollege of Life Sciences, Northwest A&F University, Yangling, Shaanxi 712100, China.
Xiao-Lei DuanCollege of Life Sciences, Northwest A&F University, Yangling, Shaanxi 712100, China.
Ming LiBeijing National Laboratory for Condensed Matter Physics and CAS Key Laboratory of Soft Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China.
Shuo-Xing DouBeijing National Laboratory for Condensed Matter Physics and CAS Key Laboratory of Soft Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China.
Xi-Miao HouCollege of Life Sciences, Northwest A&F University, Yangling, Shaanxi 712100, China houximiao@nwsuaf.edu.cn.
Xu-Guang XiCollege of Life Sciences, Northwest A&F University, Yangling, Shaanxi 712100, China Laboratoire de Biologie et Pharmacologie Appliquée, Ecole Normale Supérieure de Cachan, Centre National de la Recherche Scientifique, 61 Avenue du Président Wilson, 94235 Cachan, France xxi01@ens-cachan.fr.
Northwest A&F University · CNChinese Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alternative DNA structures that deviate from B-form double-stranded DNA such as G-quadruplex (G4) DNA can be formed by G-rich sequences that are widely distributed throughout the human genome. We have previously shown that Pif1p not only unfolds G4, but also unwinds the downstream duplex DNA in a G4-stimulated manner. In the present study, we further characterized the G4-stimulated duplex DNA unwinding phenomenon by means of single-molecule fluorescence resonance energy transfer. It was found that Pif1p did not unwind the partial duplex DNA immediately after unfolding the upstream G4 structure, but rather, it would dwell at the ss/dsDNA junction with a 'waiting time'. Further studies revealed that the waiting time was in fact related to a protein dimerization process that was sensitive to ssDNA sequence and would become rapid if the sequence is G-rich. Furthermore, we identified that the G-rich sequence, as the G4 structure, equally stimulates duplex DNA unwinding. The present work sheds new light on the molecular mechanism by which G4-unwinding helicase Pif1p resolves physiological G4/duplex DNA structures in cells.

Indexed as

BiocatalysisG-QuadruplexesNucleic Acid DenaturationBase SequenceDNADNA HelicasesDNA ReplicationDNA, Single-StrandedProtein MultimerizationSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSubstrate SpecificityTime FactorsDNADNA HelicasesDNA, Single-StrandedPIF1 protein, S cerevisiaeSaccharomyces cerevisiae Proteins

Identifiers

PMID27471032
PMCPMC5041479
OpenAlexW2483606242

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.