Evidence map›Paper›PMID 25621511›Full record

ArticleEpigenetics2015

Plasticity of DNA methylation in a nerve injury model of pain.

Meike Gölzenleuchter, Rahul Kanwar, Manal Zaibak, Fadi Al Saiegh, Theresa Hartung, Jana Klukas, Regenia L Smalley, Julie M Cunningham, Maria E Figueroa, Gary P Schroth and 3 more

Abstract read
In one paragraph

Article in Epigenetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Review
  2. The Role of Methylation Modification in Neural Injury and Repair.International journal of molecular sciences · 2025
    Review
  3. Critical Windows: Exploring the Association Between Perinatal Trauma, Epigenetics, and Chronic Pain.The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2024
    Review
  4. Review
  5. Epigenetic Landscapes of Pain: DNA Methylation Dynamics in Chronic Pain.International journal of molecular sciences · 2024
    Review
  6. The Epigenetics of Neuropathic Pain: A Systematic Update.International journal of molecular sciences · 2023
    Review
  7. Review
  8. Article
  9. Review
  10. DNA Methylation and Non-Coding RNAs during Tissue-Injury Associated Pain.International journal of molecular sciences · 2022
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Nerve Injury-Induced Chronic Pain Is Associated with Persistent DNA Methylation Reprogramming in Dorsal Root Ganglion.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

13 authors.

Meike Gölzenleuchtera Departments of Anesthesiology; Oncology; and Biostatistics and Bioinformatics; Mayo Clinic , Rochester , MN USA.
Rahul Kanwar
Manal Zaibak
Fadi Al Saiegh
Theresa Hartung
Jana Klukas
Regenia L Smalley
Julie M Cunningham
Maria E Figueroa
Gary P Schroth
Terry M Therneau
Michaela S Banck
Andreas S Beutler

Funding

DNA Methylation Profiling of Chronic PainR21NS062271 · NINDS · MAYO CLINIC ROCHESTER · PI BEUTLER, ANDREAS S. · 2009 to 2010
$403k
NINDS NIH HHS R21NS062271
6 · The paper itself

Abstract

The response of the peripheral nervous system (PNS) to injury may go together with alterations in epigenetics, a conjecture that has not been subjected to a comprehensive, genome-wide test. Using reduced representation bisulfite sequencing, we report widespread remodeling of DNA methylation in the rat dorsal root ganglion (DRG) occurring within 24 h of peripheral nerve ligation, a neuropathy model of allodynia. Significant (P < 10(-4)) cytosine hyper- and hypo-methylation was found at thousands of CpG sites. Remodeling occurred outside of CpG islands. Changes affected genes with known roles in the PNS, yet methylome remodeling also involved genes that were not linked to neuroplasticity by prior evidence. Consistent with emerging models relying on genome-wide methylation and RNA-seq analysis of promoter regions and gene bodies, variation of methylation was not tightly linked with variation of gene expression. Furthermore, approximately 44% of the dynamically changed CpGs were located outside of genes. We compared their positions with the intergenic, tissue-specific differentially methylated CpGs (tDMCs) of an independent experimental set consisting of liver, spleen, L4 control DRG, and muscle. Dynamic changes affected those intergenic CpGs that were different between tissues (P < 10(-15)) and almost never the invariant portion of the methylome (those CpGs that were identical across all tissues). Our findings-obtained in mixed tissue-show that peripheral nerve injury leads to methylome remodeling in the DRG. Future studies may address which of the cell types found in the DRG, such as specific groups of neurons or non-neuronal cells are affected by which aspect of the observed methylome remodeling.

Indexed as

DNA MethylationAnimalsCpG IslandsDisease Models, AnimalGanglia, SpinalMaleNeuronsPainRatsSpinal NervesTranscriptomedDMCs, dynamically differentially methylated CpGsdorsal root ganglionDRG, dorsal root ganglionHCP, high-CpG promoterLCP, low-CpG promotermethylationpainperipheral nervous systemratRRBSRRBS, reduced representation bisulfite sequencingSNL, spinal nerve ligationspinal nerve ligationtDMCs, tissue-specific differentially methylated CpGstIMCs, tissue-invariant methylated CpGs

Identifiers

PMID25621511
PMCPMC4622653

What OpenQuestion holds

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Registered trials

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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.