Evidence map›Paper›PMID 31750523›Full record

ArticleNucleic acids research2019

A single ChIP-seq dataset is sufficient for comprehensive analysis of motifs co-occurrence with MCOT package.

Victor Levitsky, Elena Zemlyanskaya, Dmitry Oshchepkov, Olga Podkolodnaya, Elena Ignatieva, Ivo Grosse, Victoria Mironova, Tatyana Merkulova

Abstract read
In one paragraph

Article in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. A new pipeline SPICE identifies novel JUN-IKZF1 composite elements.bioRxiv : the preprint server for biology · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Web-MCOT Server for Motif Co-Occurrence Search in ChIP-Seq Data.International journal of molecular sciences · 2022
    Article
  12. TF-COMB - Discovering grammar of transcription factor binding sites.Computational and structural biotechnology journal · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Motif grammar: The basis of the language of gene expression.Computational and structural biotechnology journal · 2020
    Review
  19. 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.

Victor LevitskyDepartment of Systems Biology, Institute of Cytology and Genetics, Novosibirsk 630090, Russia.
Elena ZemlyanskayaDepartment of Systems Biology, Institute of Cytology and Genetics, Novosibirsk 630090, Russia.
Dmitry OshchepkovDepartment of Systems Biology, Institute of Cytology and Genetics, Novosibirsk 630090, Russia.
Olga PodkolodnayaDepartment of Systems Biology, Institute of Cytology and Genetics, Novosibirsk 630090, Russia.
Elena IgnatievaDepartment of Systems Biology, Institute of Cytology and Genetics, Novosibirsk 630090, Russia.
Ivo GrosseDepartment of Natural Science, Novosibirsk State University, Novosibirsk 630090, Russia.
Victoria MironovaDepartment of Systems Biology, Institute of Cytology and Genetics, Novosibirsk 630090, Russia.
Tatyana MerkulovaDepartment of Natural Science, Novosibirsk State University, Novosibirsk 630090, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recognition of composite elements consisting of two transcription factor binding sites gets behind the studies of tissue-, stage- and condition-specific transcription. Genome-wide data on transcription factor binding generated with ChIP-seq method facilitate an identification of composite elements, but the existing bioinformatics tools either require ChIP-seq datasets for both partner transcription factors, or omit composite elements with motifs overlapping. Here we present an universal Motifs Co-Occurrence Tool (MCOT) that retrieves maximum information about overrepresented composite elements from a single ChIP-seq dataset. This includes homo- and heterotypic composite elements of four mutual orientations of motifs, separated with a spacer or overlapping, even if recognition of motifs within composite element requires various stringencies. Analysis of 52 ChIP-seq datasets for 18 human transcription factors confirmed that for over 60% of analyzed datasets and transcription factors predicted co-occurrence of motifs implied experimentally proven protein-protein interaction of respecting transcription factors. Analysis of 164 ChIP-seq datasets for 57 mammalian transcription factors showed that abundance of predicted composite elements with an overlap of motifs compared to those with a spacer more than doubled; and they had 1.5-fold increase of asymmetrical pairs of motifs with one more conservative 'leading' motif and another one 'guided'.

Indexed as

AlgorithmsAnimalsBinding SitesChromatin Immunoprecipitation SequencingComputational BiologyDatasets as TopicHumansMiceNucleotide MotifsRegulatory Elements, TranscriptionalSequence Analysis, DNATranscription FactorsTranscription Factors

Identifiers

PMID31750523
PMCPMC6868382

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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.