Evidence map›Paper›PMID 18971312›Full record

ArticleGenome research2008

DNA methylation profile of tissue-dependent and differentially methylated regions (T-DMRs) in mouse promoter regions demonstrating tissue-specific gene expression.

Shintaro Yagi, Keiji Hirabayashi, Shinya Sato, Wei Li, Yoko Takahashi, Tsutomu Hirakawa, Guoying Wu, Naoko Hattori, Naka Hattori, Jun Ohgane and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing 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

79 citing papers in PubMed, 162 citations in OpenAlex.

  1. Article
  2. Article
  3. Epigenome editing-mediated restoration ofBiochemistry and biophysics reports · 2025
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  8. Metabolic and Epigenetics Action Mechanisms of Antiobesity Medicinal Plants and Phytochemicals.Evidence-based complementary and alternative medicine : eCAM · 2021
    Review
  9. Article
  10. Direct readout of heterochromatic H3K9me3 regulates DNMT1-mediated maintenance DNA methylation.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  11. Article
  12. Article
  13. Article
  14. A Pilot Study of Aberrant CpG Island Hypermethylation ofInternational journal of medical sciences · 2019
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Drugging the pain epigenome.Nature reviews. Neurology · 2017
    Review
  20. Article

19 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

13 authors at 3 institutions in 2 countries.

Shintaro YagiLaboratory of Cellular Biochemistry, Department of Animal Resource Sciences/Veterinary Medical Sciences, The University of Tokyo, Japan.
Keiji Hirabayashi
Shinya Sato
Wei Li
Yoko Takahashi
Tsutomu Hirakawa
Guoying Wu
Naoko Hattori
Naka Hattori
Jun Ohgane
Satoshi Tanaka
X Shirley Liu
Kunio Shiota
Tokyo Medical University · JPBaylor College of Medicine · USDana-Farber Cancer Institute · US

Funding

Computational Models for Mechanisms of Global Transcription RegulationR01HG004069 · NHGRI · DANA-FARBER CANCER INST · PI LIU, XIAOLE SHIRLEY · 2006 to 2013
$3.6M
NHGRI NIH HHS R01 HG004069
6 · The paper itself

Abstract

DNA methylation constitutes an important epigenetic regulation mechanism in many eukaryotes, although the extent of DNA methylation in the regulation of gene expression in the mammalian genome is poorly understood. We developed D-REAM, a genome-wide DNA methylation analysis method for tissue-dependent and differentially methylated region (T-DMR) profiling with restriction tag-mediated amplification in mouse tissues and cells. Using a mouse promoter tiling array covering a region from -6 to 2.5 kb ( approximately 30,000 transcription start sites), we found that over 3000 T-DMRs are hypomethylated in liver compared to cerebrum. The DNA methylation profile of liver was distinct from that of kidney and spleen. This hypomethylation profile marked genes that are specifically expressed in liver, including key transcription factors such as Hnf1a and Hnf4a. Genes with T-DMRs, especially those lacking CpG islands and those with HNF-1A binding motifis in their promoters, showed good correlation between their tissue-specific expression and liver hypomethylation status. T-DMRs located downstream from their transcription start sites also showed tissue-specific gene expression. These data indicate that multilayered regulation of tissue-specific gene function could be elucidated by DNA methylation tissue profiling.

Indexed as

DNA MethylationGene Expression ProfilingGene Expression RegulationPromoter Regions, GeneticAnimalsComputational BiologyDNAGene AmplificationLiverMaleMiceMice, Inbred C57BLModels, GeneticOligonucleotide Array Sequence AnalysisSequence Analysis, DNADNA

Identifiers

PMID18971312
PMCPMC2593572
OpenAlexW2119346793

What OpenQuestion holds

Textmetadata
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.