Evidence map›Paper›PMID 23658232›Full record

ArticleNucleic acids research2013

Quantitative assessment of Tet-induced oxidation products of 5-methylcytosine in cellular and tissue DNA.

Shuo Liu, Jin Wang, Yijing Su, Candace Guerrero, Yaxue Zeng, Devarati Mitra, Philip J Brooks, David E Fisher, Hongjun Song, Yinsheng Wang

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

55 citing papers in PubMed, 136 citations in OpenAlex.

  1. Article
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  5. Review
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  13. Article
  14. Review
  15. Deformylation of 5-Formylcytidine in Different Cell Types.Angewandte Chemie (International ed. in English) · 2021
    Article
  16. The Multiple Cellular Roles of SMUG1 in Genome Maintenance and Cancer.International journal of molecular sciences · 2021
    Review
  17. Article
  18. Article
  19. Article
  20. Sequencing 5-Hydroxymethyluracil at Single-Base Resolution.Angewandte Chemie (International ed. in English) · 2018
    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

10 authors at 4 institutions in 1 country.

Shuo LiuEnvironmental Toxicology Graduate Program, University of California, Riverside, CA 92521, USA.
Jin Wang
Yijing Su
Candace Guerrero
Yaxue Zeng
Devarati Mitra
Philip J Brooks
David E Fisher
Hongjun Song
Yinsheng Wang
University of California, Riverside · USJohns Hopkins University · USNational Center for Advancing Translational Sciences · USNational Institute on Alcohol Abuse and Alcoholism · US

Funding

Integrative genetics of behavior with high throughput technologiesZIAAA000301 · NIAAA · NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM · PI GOLDMAN, DAVID · 2009 to 2025
$68.6M
Medical Scientist Training ProgramT32GM007753 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WALENSKY, LOREN DAVID · 1985 to 2021
$50.0M
The MITF transcriptional network: melanoma risk and carcinogenesisR01AR043369 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI DAVID E FISHER · 1996 to 2026
$9.4M
Chemistry and Biology of DNA CarboxyalkylationR01DK082779 · NIDDK · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI WANG, YINSHENG · 2009 to 2016
$3.0M
Neural Development of Human Induced Pluripotent Stem Cells from Schizophrenia PatR33MH087874 · NIMH · JOHNS HOPKINS UNIVERSITY · PI SONG, HONGJUN · 2011 to 2012
$805k
Impact of Bisphenol A on neural stem cells and development in the adult brainR21ES021957 · NIEHS · JOHNS HOPKINS UNIVERSITY · PI SONG, HONGJUN · 2012 to 2013
$441k
Circuitry mechanisms regulating adult hippocampal neurogenesisR56NS047344 · NINDS · JOHNS HOPKINS UNIVERSITY · PI SONG, HONGJUN · 2012 to 2012
$405k
NIAMS NIH HHS AR043369NIAMS NIH HHS R01 AR043369NICHD NIH HHS HHSN275200900011CNICHD NIH HHS N01-HD-9-0011NIDDK NIH HHS DK082779NIDDK NIH HHS R01 DK082779NIEHS NIH HHS ES021957NIEHS NIH HHS R21 ES021957NIGMS NIH HHS T32 GM007753NIMH NIH HHS R33 MH087874NINDS NIH HHS NS047344NINDS NIH HHS R56 NS047344
6 · The paper itself

Abstract

Recent studies showed that Ten-eleven translocation (Tet) family dioxygenases can oxidize 5-methyl-2'-deoxycytidine (5-mdC) in DNA to yield the 5-hydroxymethyl, 5-formyl and 5-carboxyl derivatives of 2'-deoxycytidine (5-HmdC, 5-FodC and 5-CadC). 5-HmdC in DNA may be enzymatically deaminated to yield 5-hydroxymethyl-2'-deoxyuridine (5-HmdU). After their formation at CpG dinucleotide sites, these oxidized pyrimidine nucleosides, particularly 5-FodC, 5-CadC, and 5-HmdU, may be cleaved from DNA by thymine DNA glycosylase, and subsequent action of base-excision repair machinery restores unmethylated cytosine. These processes are proposed to be important in active DNA cytosine demethylation in mammals. Here we used a reversed-phase HPLC coupled with tandem mass spectrometry (LC-MS/MS/MS) method, along with the use of stable isotope-labeled standards, for accurate measurements of 5-HmdC, 5-FodC, 5-CadC and 5-HmdU in genomic DNA of cultured human cells and multiple mammalian tissues. We found that overexpression of the catalytic domain of human Tet1 led to marked increases in the levels of 5-HmdC, 5-FodC and 5-CadC, but only a modest increase in 5-HmdU, in genomic DNA of HEK293T cells. Moreover, 5-HmdC is present at a level that is approximately 2-3 and 3-4 orders of magnitude greater than 5-FodC and 5-CadC, respectively, and 35-400 times greater than 5-HmdU in the mouse brain and skin, and human brain. The robust analytical method built a solid foundation for dissecting the molecular mechanisms of active cytosine demethylation, for measuring these 5-mdC derivatives and assessing their involvement in epigenetic regulation in other organisms and for examining whether these 5-mdC derivatives can be used as biomarkers for human diseases.

Indexed as

5-MethylcytosineAnimalsBrain ChemistryCell Line, TumorChromatography, High Pressure LiquidDeoxycytidineDioxygenasesDNADNA-Binding ProteinsHEK293 CellsHumansMiceMixed Function OxygenasesOxidation-ReductionProto-Oncogene ProteinsSkin5-formyl-2'-deoxycytidine5-hydroxymethyl-2'-deoxycytidine5-hydroxymethyl-2'-deoxyuridine5-MethylcytosineDeoxycytidineDioxygenasesDNADNA-Binding ProteinsMixed Function OxygenasesProto-Oncogene ProteinsTET1 protein, humanThymidine

Identifiers

PMID23658232
PMCPMC3711458
OpenAlexW2104687676

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

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.