Evidence map›Paper›PMID 30250250›Full record

ArticleNature2018

The interaction landscape between transcription factors and the nucleosome.

Fangjie Zhu, Lucas Farnung, Eevi Kaasinen, Biswajyoti Sahu, Yimeng Yin, Bei Wei, Svetlana O Dodonova, Kazuhiro R Nitta, Ekaterina Morgunova, Minna Taipale and 2 more

Abstract read
In one paragraph

Article in Nature, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 236 papers.

0numbers the graph read from it
0cells of the map it votes in
236citing papers in PubMed
16.0field-weighted citation impact, top 1% 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

236 citing papers in PubMed, 385 citations in OpenAlex.

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  13. Cryo-EM structure of ALC1 in an open conformation bound to a PARylated nucleosome.Acta crystallographica. Section D, Structural biology · 2026
    Article
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176 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 4 countries.

Fangjie ZhuDepartment of Biochemistry, University of Cambridge, Cambridge, UK.
Lucas FarnungMax Planck Institute for Biophysical Chemistry, Department of Molecular Biology, Göttingen, Germany.
Eevi KaasinenDivision of Functional Genomics and Systems Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Biswajyoti SahuGenome-Scale Biology Program, University of Helsinki, Helsinki, Finland.
Yimeng YinDivision of Functional Genomics and Systems Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Bei WeiDivision of Functional Genomics and Systems Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Svetlana O DodonovaMax Planck Institute for Biophysical Chemistry, Department of Molecular Biology, Göttingen, Germany.
Kazuhiro R NittaDepartment of Biosciences and Nutrition, Karolinska Institutet, Stockholm, Sweden.
Ekaterina MorgunovaDivision of Functional Genomics and Systems Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Minna TaipaleDepartment of Biochemistry, University of Cambridge, Cambridge, UK.
Patrick CramerMax Planck Institute for Biophysical Chemistry, Department of Molecular Biology, Göttingen, Germany.
Jussi TaipaleDepartment of Biochemistry, University of Cambridge, Cambridge, UK. ajt208@cam.ac.uk.
Karolinska Institutet · SEMax Planck Institute for Biophysical Chemistry · DEUniversity of Cambridge · GBUniversity of Helsinki · FI

Funding

European Research Council 693023
6 · The paper itself

Abstract

Nucleosomes cover most of the genome and are thought to be displaced by transcription factors in regions that direct gene expression. However, the modes of interaction between transcription factors and nucleosomal DNA remain largely unknown. Here we systematically explore interactions between the nucleosome and 220 transcription factors representing diverse structural families. Consistent with earlier observations, we find that the majority of the studied transcription factors have less access to nucleosomal DNA than to free DNA. The motifs recovered from transcription factors bound to nucleosomal and free DNA are generally similar. However, steric hindrance and scaffolding by the nucleosome result in specific positioning and orientation of the motifs. Many transcription factors preferentially bind close to the end of nucleosomal DNA, or to periodic positions on the solvent-exposed side of the DNA. In addition, several transcription factors usually bind to nucleosomal DNA in a particular orientation. Some transcription factors specifically interact with DNA located at the dyad position at which only one DNA gyre is wound, whereas other transcription factors prefer sites spanning two DNA gyres and bind specifically to each of them. Our work reveals notable differences in the binding of transcription factors to free and nucleosomal DNA, and uncovers a diverse interaction landscape between transcription factors and the nucleosome.

Indexed as

AnimalsBase SequenceDNAHumansMiceModels, MolecularNucleosomesNucleotide MotifsProtein BindingRotationSELEX Aptamer TechniqueTranscription FactorsDNANucleosomesTranscription Factors

Identifiers

PMID30250250
PMCPMC6173309
OpenAlexW2951091094

What OpenQuestion holds

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Read underepoch 390

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.