Evidence map›Paper›PMID 24669905›Full record

ArticleBMC genomics2014

Chromatin states reveal functional associations for globally defined transcription start sites in four human cell lines.

Morten Rye, Geir Kjetil Sandve, Carsten O Daub, Hideya Kawaji, Piero Carninci, Alistair R R Forrest, Finn Drabløs, FANTOM consortium

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

9 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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  4. The role of the genome in experience-dependent plasticity: Extending the analogy of the genomic action potential.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Review
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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 5 institutions in 4 countries.

Morten RyeDepartment of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology, P,O, Box 8905, NO-7491 Trondheim, Norway. morten.rye@ntnu.no.
Geir Kjetil Sandve
Carsten O Daub
Hideya Kawaji
Piero Carninci
Alistair R R Forrest
Finn Drabløs
FANTOM consortium
Center for Genomic Science · ITNorwegian University of Science and Technology · NOCE Technologies (United Kingdom) · GBRIKEN Center for Integrative Medical Sciences · JPUniversity of Oslo · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDeciphering the most common modes by which chromatin regulates transcription, and how this is related to cellular status and processes is an important task for improving our understanding of human cellular biology. The FANTOM5 and ENCODE projects represent two independent large scale efforts to map regulatory and transcriptional features to the human genome. Here we investigate chromatin features around a comprehensive set of transcription start sites in four cell lines by integrating data from these two projects.

resultsTranscription start sites can be distinguished by chromatin states defined by specific combinations of both chromatin mark enrichment and the profile shapes of these chromatin marks. The observed patterns can be associated with cellular functions and processes, and they also show association with expression level, location relative to nearby genes, and CpG content. In particular we find a substantial number of repressed inter- and intra-genic transcription start sites enriched for active chromatin marks and Pol II, and these sites are strongly associated with immediate-early response processes and cell signaling. Associations between start sites with similar chromatin patterns are validated by significant correlations in their global expression profiles.

conclusionsThe results confirm the link between chromatin state and cellular function for expressed transcripts, and also indicate that active chromatin states at repressed transcripts may poise transcripts for rapid activation during immune response.

Indexed as

Transcription Initiation SiteAlgorithmsCell Line, TumorChromatinChromatin ImmunoprecipitationCluster AnalysisComputational BiologyCpG IslandsGene Expression RegulationGene LibraryHeLa CellsHep G2 CellsHistonesHumansK562 CellsPrincipal Component AnalysisChromatinHistonesTranscription Factors

Identifiers

PMID24669905
PMCPMC3986914
OpenAlexW2063111950

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.