Evidence map›Paper›PMID 25406324›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Simultaneous sequencing of oxidized methylcytosines produced by TET/JBP dioxygenases in Coprinopsis cinerea.

Lukas Chavez, Yun Huang, Khai Luong, Suneet Agarwal, Lakshminarayan M Iyer, William A Pastor, Virginia K Hench, Sylvia A Frazier-Bowers, Evgenia Korol, Shuo Liu and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

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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

17 authors at 10 institutions in 1 country.

Lukas ChavezDivision of Signaling and Gene Expression, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037; Sanford Consortium for Regenerative Medicine, La Jolla, CA 92037;
Yun HuangDivision of Signaling and Gene Expression, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037; Sanford Consortium for Regenerative Medicine, La Jolla, CA 92037;
Khai LuongPacific Biosciences, Menlo Park, CA 94025;
Suneet AgarwalDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA 02115;
Lakshminarayan M IyerNational Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD 20894;
William A PastorDivision of Signaling and Gene Expression, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037;
Virginia K HenchDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599;
Sylvia A Frazier-BowersDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599;
Evgenia KorolSkirball Institute, NYU Langone Medical Center, New York University, New York, NY 10016;
Shuo LiuEnvironmental Toxicology Graduate Program and Department of Chemistry, University of California, Riverside, CA 92521; and.
Mamta TahilianiSkirball Institute, NYU Langone Medical Center, New York University, New York, NY 10016;
Yinsheng WangEnvironmental Toxicology Graduate Program and Department of Chemistry, University of California, Riverside, CA 92521; and.
Tyson A ClarkPacific Biosciences, Menlo Park, CA 94025;
Jonas KorlachPacific Biosciences, Menlo Park, CA 94025;
Patricia J PukkilaDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599;
L AravindNational Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD 20894;
Anjana RaoDivision of Signaling and Gene Expression, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037; Department of Pharmacology and Moores Cancer Center, University of California, San Diego, La Jolla, CA 92093 arao@liai.org.
La Jolla Institute for Immunology · USPacific Biosciences (United States) · USUniversity of North Carolina at Chapel Hill · USUniversity of California, Riverside · USDana-Farber Cancer Institute · USNational Center for Biotechnology Information · USNational Institutes of Health · USNew York University · USNYU Langone Health · USUniversity of California, San Diego · US

Funding

HARVARD CLINICAL AND TRANSLATIONAL SCIENCE CENTER (UL1)UL1RR025758 · NCRR · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2008 to 2011
$91.4M
Evolutionary Analysis and Comparative Genomics of Protein SuperfamiliesZIALM594244 · NLM · NATIONAL LIBRARY OF MEDICINE · PI ARAVIND, L · 2009 to 2025
$20.3M
REGULATED ACCESSIBILITY OF A CYTOKINE GENE LOCUSR01AI044432 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI RAO, ANJANA · 1999 to 2014
$7.7M
Oxidative DNA Damage and CpG MutagenesisR01CA101864 · NCI · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI WANG, YINSHENG · 2004 to 2015
$2.8M
Role of TET proteins in myeloid malignanciesR01CA151535 · NCI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI RAO, ANJANA · 2012 to 2016
$1.8M
Role of TET Proteins in ES Cell Pluripotency and FunctionR01HD065812 · NICHD · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI RAO, ANJANA · 2011 to 2015
$1.8M
Molecular mechanisms of nuclear reprogrammingK08HL089150 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI AGARWAL, SUNEET · 2008 to 2012
$662k
Howard Hughes Medical InstituteIntramural NIH HHSNCI NIH HHS R01 CA101864NCI NIH HHS R01 CA151535NCRR NIH HHS 1 UL1 RR 025758-02NCRR NIH HHS UL1 RR025758NHLBI NIH HHS K08 HL089150NIAID NIH HHS R01 AI044432NIAID NIH HHS R01 AI44432NICHD NIH HHS R01 HD065812
6 · The paper itself

Abstract

TET/JBP enzymes oxidize 5-methylpyrimidines in DNA. In mammals, the oxidized methylcytosines (oxi-mCs) function as epigenetic marks and likely intermediates in DNA demethylation. Here we present a method based on diglucosylation of 5-hydroxymethylcytosine (5hmC) to simultaneously map 5hmC, 5-formylcytosine, and 5-carboxylcytosine at near-base-pair resolution. We have used the method to map the distribution of oxi-mC across the genome of Coprinopsis cinerea, a basidiomycete that encodes 47 TET/JBP paralogs in a previously unidentified class of DNA transposons. Like 5-methylcytosine residues from which they are derived, oxi-mC modifications are enriched at centromeres, TET/JBP transposons, and multicopy paralogous genes that are not expressed, but rarely mark genes whose expression changes between two developmental stages. Our study provides evidence for the emergence of an epigenetic regulatory system through recruitment of selfish elements in a eukaryotic lineage, and describes a method to map all three different species of oxi-mCs simultaneously.

Indexed as

5-MethylcytosineBasidiomycotaChromosomes, FungalDioxygenasesDNA MethylationDNA Transposable ElementsFungal ProteinsGene Expression Regulation, DevelopmentalGene Expression Regulation, FungalGenome, FungalHEK293 CellsHumansHyphaeOxidation-ReductionSequence AnalysisSpores, Fungal5-MethylcytosineDioxygenasesDNA Transposable ElementsFungal Proteins5caC5fC5mCSMRT-seqTET

Identifiers

PMID25406324
PMCPMC4260599
OpenAlexW2022764597

What OpenQuestion holds

Textmetadata
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.