Evidence map›Paper›PMID 23937714›Full record

ArticleBMC genomics2013

Genome-wide profiling identifies a subset of methamphetamine (METH)-induced genes associated with METH-induced increased H4K5Ac binding in the rat striatum.

Jean Lud Cadet, Subramaniam Jayanthi, Michael T McCoy, Bruce Ladenheim, Fabienne Saint-Preux, Elin Lehrmann, Supriyo De, Kevin G Becker, Christie Brannock

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

36 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
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  11. Epigenetics of addiction.Neurochemistry international · 2021
    Review
  12. Article
  13. Article
  14. Potassium Channels and Their Potential Roles in Substance Use Disorders.International journal of molecular sciences · 2021
    Review
  15. Article
  16. Review
  17. Article
  18. Article
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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

9 authors at 3 institutions in 1 country.

Jean Lud CadetMolecular Neuropsychiatry Research Branch, DHHS/NIH/NIDA Intramural Research Program, 251 Bayview Boulevard, Baltimore, MD 21224, USA. jcadet@intra.nida.nih.gov
Subramaniam Jayanthi
Michael T McCoy
Bruce Ladenheim
Fabienne Saint-Preux
Elin Lehrmann
Supriyo De
Kevin G Becker
Christie Brannock
United States Department of Health and Human Services · USNational Institute on Aging · USNational Institutes of Health · US

Funding

Neurotoxicity in the adult rat following chronic exposure to methamphetamineZIADA000552 · NIDA · NATIONAL INSTITUTE ON DRUG ABUSE · PI CADET, JEAN LUD · 2009 to 2025
$34.3M
Analysis of complex biological systems by microarray based gene expressionZICAG000616 · NIA · NATIONAL INSTITUTE ON AGING · PI DE, SUPRIYO · 2009 to 2025
$15.5M
Intramural NIH HHS
6 · The paper itself

Abstract

backgroundMETH is an illicit drug of abuse that influences gene expression in the rat striatum. Histone modifications regulate gene transcription.

methodsWe therefore used microarray analysis and genome-scale approaches to examine potential relationships between the effects of METH on gene expression and on DNA binding of histone H4 acetylated at lysine 4 (H4K5Ac) in the rat dorsal striatum of METH-naïve and METH-pretreated rats.

resultsAcute and chronic METH administration caused differential changes in striatal gene expression. METH also increased H4K5Ac binding around the transcriptional start sites (TSSs) of genes in the rat striatum. In order to relate gene expression to histone acetylation, we binned genes of similar expression into groups of 100 genes and proceeded to relate gene expression to H4K5Ac binding. We found a positive correlation between gene expression and H4K5Ac binding in the striatum of control rats. Similar correlations were observed in METH-treated rats. Genes that showed acute METH-induced increased expression in saline-pretreated rats also showed METH-induced increased H4K5Ac binding. The acute METH injection caused similar increases in H4K5Ac binding in METH-pretreated rats, without affecting gene expression to the same degree. Finally, genes that showed METH-induced decreased expression exhibited either decreases or no changes in H4K5Ac binding.

conclusionAcute METH injections caused increased gene expression of genes that showed increased H4K5Ac binding near their transcription start sites.

Indexed as

Gene Expression ProfilingAcetylationAnimalsChromatin ImmunoprecipitationCorpus StriatumCytoskeletal ProteinsGene Expression RegulationGene Regulatory NetworksGenome-Wide Association StudyHistonesMaleMethamphetamineNerve Tissue ProteinsProtein BindingProto-Oncogene Proteins c-fosRatsactivity regulated cytoskeletal-associated proteinCytoskeletal ProteinsHistonesMethamphetamineNerve Tissue ProteinsProto-Oncogene Proteins c-fos

Identifiers

PMID23937714
PMCPMC3751638
OpenAlexW2121579679

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.