Evidence map›Paper›PMID 22639700›Full record

ArticleBiomolecular concepts2012

Mitochondrial DNA: A Blind Spot in Neuroepigenetics.

Hari Manev, Svetlana Dzitoyeva, Hu Chen

Open access · bronzeAbstract read
In one paragraph

Article in Biomolecular concepts, 2012. 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
2.8field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 44 citations in OpenAlex.

  1. Mitoepigenetic Alterations in Early-Onset Parkinson's Disease.International journal of molecular sciences · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Role of oxidative stress in epigenetic modification of MMP-9 promoter in the development of diabetic retinopathy.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2017
    Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. The epigenetics of aging and neurodegeneration.Progress in neurobiology · 2015
    Review
  13. Article
  14. Analysis of pollutant-induced changes in mitochondrial DNA methylation.Methods in molecular biology (Clifton, N.J.) · 2015
    Article
  15. Review
  16. Review
  17. The control region of mitochondrial DNA shows an unusual CpG and non-CpG methylation pattern.DNA research : an international journal for rapid publication of reports on genes and genomes · 2013
    Article
  18. Review
  19. Article
  20. Effect of valproic acid on mitochondrial epigenetics.European journal of pharmacology · 2012
    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

3 authors at 1 institution in 1 country.

Hari ManevThe Psychiatric Institute, Department of Psychiatry, University of Illinois at Chicago, Chicago, IL 60612, USA.
Svetlana Dzitoyeva
Hu Chen
University of Illinois Chicago · US

Funding

AGING AND NEURONAL 5 LIPOXYGENASER01AG015347 · NIA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MANEV, HARI · 1999 to 2010
$1.5M
NIA NIH HHS R01 AG015347
6 · The paper itself

Abstract

Neuroepigenetics, which includes nuclear DNA modifications such as 5-methylcytosine and 5-hydoxymethylcytosine and modifications of nuclear proteins such as histones, is emerging as the leading field in molecular neuroscience. Historically, a functional role for epigenetic mechanisms, including in neuroepigenetics, has been sought in the area of the regulation of nuclear transcription. However, one important compartment of mammalian cell DNA, different from nuclear but equally important for physiological and pathological processes (including in the brain), mitochondrial DNA has for the most part not had a systematic epigenetic characterization. The importance of mitochondria and mitochondrial DNA (particularly its mutations) in central nervous system physiology and pathology has long been recognized. Only recently have mechanisms of mitochondrial DNA methylation and hydroxymethylation, including the discovery of mitochondrial DNA-methyltransferases and the presence and the functionality of 5-methylcytosine and 5-hydroxymethylcytosine in mitochondrial DNA (e.g., in modifying the transcription of mitochondrial genome), been unequivocally recognized as a part of mammalian mitochondrial physiology. Here we summarize for the first time evidence supporting the existence of these mechanisms and we propose the term "mitochondrial epigenetics" to be used when referring to them. Currently, neuroepigenetics does not include mitochondrial epigenetics - a gap that we expect to close in the near future.

Identifiers

PMID22639700
PMCPMC3359012
OpenAlexW2078302635

What OpenQuestion holds

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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.