Evidence map›Paper›PMID 19276205›Full record

ArticleNucleic acids research2009

Human genomic Z-DNA segments probed by the Z alpha domain of ADAR1.

Heng Li, Jie Xiao, Jinming Li, Le Lu, Shu Feng, Peter Dröge

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

47 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The Roles of Topoisomerases in Transcriptional Regulation.International journal of molecular sciences · 2026
    Review
  5. Formation and biological implications of Z-DNA.Trends in genetics : TIG · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Methods to Study Z-DNA-Induced Genetic Instability.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  16. Thermogenomic Analysis of Left-Handed Z-DNA Propensities in Genomes.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  17. DeepZ: A Deep Learning Approach for Z-DNA Prediction.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  18. Detection of Z-DNA Structures in Supercoiled Genome.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  19. Human Heme Oxygenase-1 Promoter Activity Is Mediated by Z-DNA Formation.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  20. Review
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

6 authors at 3 institutions in 3 countries.

Heng LiDivision of Genomics and Genetics, School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive, Singapore.
Jie Xiao
Jinming Li
Le Lu
Shu Feng
Peter Dröge
Tsinghua University · CNNanyang Technological University · SGInstitut thématique Génétique, génomique et bioinformatique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Double-stranded DNA is a dynamic molecule that adopts different secondary structures. Experimental evidence indicates Z-DNA plays roles in DNA transactions such as transcription, chromatin remodeling and recombination. Furthermore, our computational analysis revealed that sequences with high Z-DNA forming potential at moderate levels of DNA supercoiling are enriched in human promoter regions. However, the actual distribution of Z-DNA segments in genomes of mammalian cells has been elusive due to the unstable nature of Z-DNA and lack of specific probes. Here we present a first human genome map of most stable Z-DNA segments obtained with A549 tumor cells. We used the Z-DNA binding domain, Z alpha, of the RNA editing enzyme ADAR1 as probe in conjunction with a novel chromatin affinity precipitation strategy. By applying stringent selection criteria, we identified 186 genomic Z-DNA hotspots. Interestingly, 46 hotspots were located in centromeres of 13 human chromosomes. There was a very strong correlation between these hotspots and high densities of single nucleotide polymorphism. Our study indicates that genetic instability and rapid evolution of human centromeres might, at least in part, be driven by Z-DNA segments. Contrary to in silico predictions, however, we found that only two of the 186 hotspots were located in promoter regions.

Indexed as

Genome, HumanAdenosine DeaminaseBinding SitesCell Line, TumorDNA, Z-FormHumansMolecular ProbesPolymorphism, Single NucleotideProtein Structure, TertiaryRNA-Binding ProteinsSequence Analysis, DNASoftwareADARB1 protein, humanAdenosine DeaminaseDNA, Z-FormMolecular ProbesRNA-Binding Proteins

Identifiers

PMID19276205
PMCPMC2677879
OpenAlexW2039287748

What OpenQuestion holds

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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.