Evidence map›Paper›PMID 27583369›Full record

ArticlePloS one2016

Cell-Wide DNA De-Methylation and Re-Methylation of Purkinje Neurons in the Developing Cerebellum.

Feng C Zhou, Marisol Resendiz, Chiao-Ling Lo, Yuanyuan Chen

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Cell identity and 5-hydroxymethylcytosine.Epigenetics & chromatin · 2025
    Review
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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

4 authors at 2 institutions in 1 country.

Feng C ZhouDepartment of Anatomy & Cell Biology, Indiana University School of Medicine, Indianapolis, Indiana, 46202, United States of America.
Marisol ResendizStark Neuroscience Research Institute, Indiana University School of Medicine, Indianapolis, Indiana, 46202, United States of America.
Chiao-Ling LoDepartment of Anatomy & Cell Biology, Indiana University School of Medicine, Indianapolis, Indiana, 46202, United States of America.
Yuanyuan ChenDepartment of Anatomy & Cell Biology, Indiana University School of Medicine, Indianapolis, Indiana, 46202, United States of America.
Indiana University – Purdue University Indianapolis · USIndiana University School of Medicine

Funding

Indiana Clinical and Translational Sciences InstituteUL1TR001108 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENNE, SCOTT C., SHEKHAR, ANANTHA · 2013 to 2017
$23.3M
RAT RESEARCH COMPONENTP50AA007611 · NIAAA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI BOSRON, WILLIAM F · 1987 to 2002
$5.3M
Epigenetics of fetal alcohol syndromeR01AA016698 · NIAAA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI ZHOU, FENG C. · 2006 to 2009
$1.1M
Translational Epigenetic Markers for Early Diagnosis of FASDR21AA024216 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI REITER, JILL L, ZHOU, FENG C. · 2016 to 2017
$413k
NCATS NIH HHS UL1 TR001108NIAAA NIH HHS P50 AA007611NIAAA NIH HHS R01 AA016698NIAAA NIH HHS R21 AA024216
6 · The paper itself

Abstract

Global DNA de-methylation is thought to occur only during pre-implantation and gametogenesis in mammals. Scalable, cell-wide de-methylation has not been demonstrated beyond totipotent stages. Here, we observed a large scale de-methylation and subsequent re-methylation (CDR) (including 5-methylcytosine (5mC) and 5-hydroxylmethylcytosine (5hmC)) in post-mitotic cerebellar Purkinje cells (PC) through the course of normal development. Through single cell immuno-identification and cell-specific quantitative methylation assays, we demonstrate that the CDR event is an intrinsically scheduled program, occurring in nearly every PC. Meanwhile, cerebellar granule cells and basket interneurons adopt their own DNA methylation program, independent of PCs. DNA de-methylation was further demonstrated at the gene level, on genes pertinent to PC development. The PC, being one of the largest neurons in the brain, may showcase an amplified epigenetic cycle which may mediate stage transformation including cell cycle arrest, vast axonal-dendritic growth, and synaptogenesis at the onset of neuronal specificity. This discovery is a key step toward better understanding the breadth and role of DNA methylation and de-methylation during neural ontology.

Indexed as

DNA MethylationAnimalsCell NucleusCerebellumChromatin Assembly and DisassemblyMicePurkinje CellsSingle-Cell Analysis

Identifiers

PMID27583369
PMCPMC5008790
OpenAlexW2518103190

What OpenQuestion holds

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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.