Evidence map›Paper›PMID 28505093›Full record

ReviewGenes2017

The Crucial Role of DNA Methylation and MeCP2 in Neuronal Function.

Maria Fasolino, Zhaolan Zhou

Open access · goldAbstract readReview
In one paragraph

Review in Genes, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
7.7field-weighted citation impact, top 3% 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

42 citing papers in PubMed, 73 citations in OpenAlex.

  1. Trial
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  16. Literature Cases Summarized Based on Their Polysomnographic Findings in Rett Syndrome.International journal of environmental research and public health · 2022
    Review
  17. Multimodal Neuroimaging in Rett Syndrome WithFrontiers in neurology · 2022
    Review
  18. Article
  19. Article
  20. Review
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

2 authors at 1 institution in 1 country.

Maria FasolinoDepartment of Genetics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA. fasolino@mail.med.upenn.edu.
Zhaolan ZhouDepartment of Genetics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA. zhaolan@mail.med.upenn.edu.
University of Pennsylvania · US

Funding

Understanding the Pathogenic Mechanisms of Rett SyndromeR01NS081054 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI Zhaolan Zhou · 2013 to 2026
$5.6M
Defining the Epigenetic Architecture Associated with Early-Life StressR01MH091850 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI ZHOU, ZHAOLAN · 2010 to 2014
$2.4M
Understanding the Epigenetic Mechanisms Underlying Stress-Related Neuropsychiatric DisordersR56MH111719 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI ZHOU, ZHAOLAN · 2017 to 2017
$586k
NIMH NIH HHS R01 MH091850NIMH NIH HHS R56 MH111719NINDS NIH HHS R01 NS081054
6 · The paper itself

Abstract

A neuron is unique in its ability to dynamically modify its transcriptional output in response to synaptic activity while maintaining a core gene expression program that preserves cellular identity throughout a lifetime that is longer than almost every other cell type in the body. A contributing factor to the immense adaptability of a neuron is its unique epigenetic landscape that elicits locus-specific alterations in chromatin architecture, which in turn influences gene expression. One such epigenetic modification that is sensitive to changes in synaptic activity, as well as essential for maintaining cellular identity, is DNA methylation. The focus of this article is on the importance of DNA methylation in neuronal function, summarizing recent studies on critical players in the establishment of (the "writing"), the modification or erasure of (the "editing"), and the mediation of (the "reading") DNA methylation in neurodevelopment and neuroplasticity. One "reader" of DNA methylation in particular, methyl-CpG-binding protein 2 (MeCP2), is highlighted, given its undisputed importance in neuronal function.

Indexed as

5-hydroxymethylcytosine (5hmC)5-methylcytosine (5mC)DNA methylationDNA methyltransferase (DNMT)long-term potentiation (LTP)methyl-CpG-binding protein 2 (MeCP2)neuroplasticityRett Syndrome (RTT)ten-eleven translocation (TET) methylcytosine dioxygenase

Identifiers

PMID28505093
PMCPMC5448015
OpenAlexW2613970646

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.