Evidence map›Paper›PMID 30266094›Full record

ArticleGenome biology2018

A comprehensive analysis of 195 DNA methylomes reveals shared and cell-specific features of partially methylated domains.

Abdulrahman Salhab, Karl Nordström, Gilles Gasparoni, Kathrin Kattler, Peter Ebert, Fidel Ramirez, Laura Arrigoni, Fabian Müller, Julia K Polansky, Cristina Cadenas and 5 more

Abstract read
In one paragraph

Article in Genome biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing 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

62 citing papers in PubMed.

  1. EpiATLAS - a reference for human epigenomic research.bioRxiv : the preprint server for biology · 2026
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2 more citing papers are in PubMed but not listed here.

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

15 authors.

Abdulrahman SalhabDepartment of Genetics, Saarland University, Campus Saarbrücken, Saarbrücken, 66123, Germany.
Karl NordströmDepartment of Genetics, Saarland University, Campus Saarbrücken, Saarbrücken, 66123, Germany.
Gilles GasparoniDepartment of Genetics, Saarland University, Campus Saarbrücken, Saarbrücken, 66123, Germany.
Kathrin KattlerDepartment of Genetics, Saarland University, Campus Saarbrücken, Saarbrücken, 66123, Germany.
Peter EbertDepartment of Computational Biology and Applied Algorithmics, Max Planck Institute for Informatics, Saarbrücken, 66123, Germany.
Fidel RamirezMax Planck Institute of Immunobiology and Epigenetics, Freiburg, 79108, Germany.
Laura ArrigoniMax Planck Institute of Immunobiology and Epigenetics, Freiburg, 79108, Germany.
Fabian MüllerDepartment of Computational Biology and Applied Algorithmics, Max Planck Institute for Informatics, Saarbrücken, 66123, Germany.
Julia K PolanskyBerlin-Brandenburg Center for Regenerative Therapies at the Charité, Berlin, Germany.
Cristina CadenasLeibniz Research Center for working Environment and Human Factors IfADo, Dortmund, 44139, Germany.
Jan G HengstlerLeibniz Research Center for working Environment and Human Factors IfADo, Dortmund, 44139, Germany.
Thomas LengauerDepartment of Computational Biology and Applied Algorithmics, Max Planck Institute for Informatics, Saarbrücken, 66123, Germany.
Thomas MankeMax Planck Institute of Immunobiology and Epigenetics, Freiburg, 79108, Germany.
DEEP Consortium
Jörn WalterDepartment of Genetics, Saarland University, Campus Saarbrücken, Saarbrücken, 66123, Germany. j.walter@mx.uni-saarland.de.ORCID 0000-0003-0563-7417

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPartially methylated domains are extended regions in the genome exhibiting a reduced average DNA methylation level. They cover gene-poor and transcriptionally inactive regions and tend to be heterochromatic. We present a comprehensive comparative analysis of partially methylated domains in human and mouse cells, to identify structural and functional features associated with them.

resultsPartially methylated domains are present in up to 75% of the genome in human and mouse cells irrespective of their tissue or cell origin. Each cell type has a distinct set of partially methylated domains, and genes expressed in such domains show a strong cell type effect. The methylation level varies between cell types with a more pronounced effect in differentiating and replicating cells. The lowest level of methylation is observed in highly proliferating and immortal cancer cell lines. A decrease of DNA methylation within partially methylated domains tends to be linked to an increase in heterochromatic histone marks and a decrease of gene expression. Characteristic combinations of heterochromatic signatures in partially methylated domains are linked to domains of early and middle S-phase and late S-G2 phases of DNA replication.

conclusionsPartially methylated domains are prominent signatures of long-range epigenomic organization. Integrative analysis identifies them as important general, lineage- and cell type-specific topological features. Changes in partially methylated domains are hallmarks of cell differentiation, with decreased methylation levels and increased heterochromatic marks being linked to enhanced cell proliferation. In combination with broad histone marks, partially methylated domains demarcate distinct domains of late DNA replication.

Indexed as

AnimalsCell LineDNA MethylationDNA ReplicationGenome, HumanHeterochromatinHumansMiceNeoplasmsOrgan SpecificityTranscription, GeneticHeterochromatinHeterochromatinPartially methylated domainsProliferationReplication timing

Identifiers

PMID30266094
PMCPMC6161375

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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.