Evidence map›Paper›PMID 27008990›Full record

ArticleGene2016

Non-random distribution of methyl-CpG sites and non-CpG methylation in the human rDNA promoter identified by next generation bisulfite sequencing.

Maciej Pietrzak, Grzegorz A Rempala, Peter T Nelson, Michal Hetman

Open access · bronzeAbstract read
In one paragraph

Article in Gene, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Epigenetics of the Synapse in Neurodegeneration.Current neurology and neuroscience reports · 2019
    Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Epigenetic roles in the malignant transformation of gastric mucosal cells.Cellular and molecular life sciences : CMLS · 2016
    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

4 authors at 3 institutions in 1 country.

Maciej PietrzakKentucky Spinal Cord Injury Research Center, University of Louisville, Louisville, KY 40292, United States; Department of Neurological Surgery, University of Louisville, Louisville, KY 40292, United States.
Grzegorz A RempalaDivision of Biostatistics and Mathematical Biosciences Institute, The Ohio State University, Columbus, OH 43210, United States.
Peter T NelsonSanders-Brown Center on Aging, University of Kentucky, Lexington, KY 40536, United States.
Michal HetmanKentucky Spinal Cord Injury Research Center, University of Louisville, Louisville, KY 40292, United States; Department of Neurological Surgery, University of Louisville, Louisville, KY 40292, United States; Department of Pharmacology & Toxicology, University of Louisville, Louisville, KY 40292, United States. Electronic address: michal.hetman@louisville.edu.
University of Louisville · USThe Ohio State University · USUniversity of Kentucky · US

Funding

University of Kentucky Alzheimer's Disease Core Center - Biomarker CoreP30AG028383 · NIA · UNIVERSITY OF KENTUCKY · PI SCHMITT, FREDERICK · 2006 to 2020
$23.3M
Mechanisms of plasticity and repair after SCIP30GM103507 · NIGMS · UNIVERSITY OF LOUISVILLE · PI WHITTEMORE, SCOTT R · 2012 to 2015
$4.2M
ER stress and oligodendrocyte survival after spinal cord injuryR01NS073584 · NINDS · UNIVERSITY OF LOUISVILLE · PI HETMAN, MICHAL, WHITTEMORE, SCOTT R · 2011 to 2015
$2.1M
Statistical Methods for Analyzing Antigen Receptors DataR01CA152158 · NCI · OHIO STATE UNIVERSITY · PI REMPALA, GRZEGORZ A · 2010 to 2014
$1.1M
NCI NIH HHS CA152158NCI NIH HHS R01 CA152158NIA NIH HHS AG028383NIA NIH HHS P30 AG028383NICHD NIH HHS HHSN275200900011CNIGMS NIH HHS 8P30GM103507NIGMS NIH HHS P30 GM103507NINDS NIH HHS NS073584-01NINDS NIH HHS R01 NS073584
6 · The paper itself

Abstract

A next generation bisulfite sequencing (NGBS) was used to study rDNA promoter methylation in human brain using postmortem samples of the parietal cortex. Qualitative analysis of patterns of CpG methylation was performed at the individual rDNA unit level. CpG site-specific differences in methylation frequency were observed with the core promoter harboring three out of four most methylated CpGs. Moreover, there was an overall trend towards co-methylation for all possible pairs of 26 CpG sites. The hypermethylated CpGs from the core promoter were also most likely to be co-methylated. Finally, although rare, non-CpG (CpH) methylation was detected at several sites with one of them confirmed using the PspGI-qPCR assay. Similar trends were observed in samples from control individuals as well as patients suffering of Alzheimer's disease (AD), mild cognitive impairment (MCI) or ataxia telangiectasia (AT). Taken together, while some methyl-CpG sites including those in the core promoter may have relatively greater inhibitory effect on rRNA transcription, co-methylation at multiple sites may be required for full and/or long lasting silencing of human rDNA.

Indexed as

Alzheimer DiseaseAtaxia TelangiectasiaBase SequenceBrainCognitive DysfunctionCpG IslandsDNA MethylationDNA, RibosomalHigh-Throughput Nucleotide SequencingHumansNeurodegenerative DiseasesPromoter Regions, GeneticSequence Analysis, DNADNA, RibosomalAgingBrainDNA methylationNeurodegenerationNucleolusrDNA

Identifiers

PMID27008990
PMCPMC4934664
OpenAlexW2304608235

What OpenQuestion holds

Textmetadata
LicenceTDM
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.