Evidence map›Paper›PMID 31431505›Full record

ArticleThe Journal of biological chemistry2019

Genome-wide mapping of regions preferentially targeted by the human DNA-cytosine deaminase APOBEC3A using uracil-DNA pulldown and sequencing.

Ramin Sakhtemani, Vimukthi Senevirathne, Jessica Stewart, Madusha L W Perera, Roger Pique-Regi, Michael S Lawrence, Ashok S Bhagwat

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Distinct repair processes produce APOBEC-induced deletions, tandem substitutions, and complex mutations in yeast and human cells.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  6. Review
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  8. Article
  9. Genome-wide mapping of genomic DNA damage: methods and implications.Cellular and molecular life sciences : CMLS · 2021
    Review
  10. Article
  11. Article
  12. Detection of Genomic Uracil Patterns.International journal of molecular sciences · 2021
    Review
  13. Article
  14. Article
  15. 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

7 authors at 2 institutions in 1 country.

Ramin SakhtemaniDepartment of Chemistry, Wayne State University, Detroit, Michigan 48202.
Vimukthi SenevirathneDepartment of Chemistry, Wayne State University, Detroit, Michigan 48202.
Jessica StewartDepartment of Chemistry, Wayne State University, Detroit, Michigan 48202.
Madusha L W PereraDepartment of Chemistry, Wayne State University, Detroit, Michigan 48202.
Roger Pique-RegiCenter for Molecular Medicine and Genetics, Wayne State University, Wayne State University School of Medicine, Detroit, Michigan 48201.
Michael S LawrenceDepartment of Pathology and Cancer Center, Massachusetts General Hospital, Boston, Massachusetts 02114.
Ashok S BhagwatDepartment of Chemistry, Wayne State University, Detroit, Michigan 48202 axb@chem.wayne.edu.ORCID 0000-0003-1188-0579
Wayne State University · USMassachusetts General Hospital · US

Funding

TRANSCRIPTION--INDUCED MUTATIONSR01GM057200 · NIGMS · WAYNE STATE UNIVERSITY · PI BHAGWAT, ASHOK S · 1998 to 2014
$2.6M
Mapping and Visualizing Uracils Created by AID/APOBEC Enzymes using UdgXR21AI144708 · NIAID · WAYNE STATE UNIVERSITY · PI BHAGWAT, ASHOK S · 2019 to 2020
$398k
NIAID NIH HHS R21 AI144708NIGMS NIH HHS R01 GM057200
6 · The paper itself

Abstract

Activation-induced deaminase (AID) and apolipoprotein B mRNA-editing enzyme catalytic subunit (APOBEC) enzymes convert cytosines to uracils, creating signature mutations that have been used to predict sites targeted by these enzymes. Mutation-based targeting maps are distorted by the error-prone or error-free repair of these uracils and by selection pressures. To directly map uracils created by AID/APOBEC enzymes, here we used uracil-DNA glycosylase and an alkoxyamine to covalently tag and sequence uracil-containing DNA fragments (UPD-Seq). We applied this technique to the genome of repair-defective, APOBEC3A-expressing bacterial cells and created a uracilation genome map,

Indexed as

Chromosome MappingGenomicsSequence Analysis, DNABase SequenceCytidine DeaminaseCytosineDNA, BacterialEscherichia coliHumansMutationProteinsSubstrate SpecificityTranscription, GeneticUracilAPOBEC3A protein, humanCytidine DeaminaseCytosineDNA, BacterialProteinsUracilAID/APOBECbase excision repair (BER)ChIP-sequencing (ChIP-seq)cytosine deaminaseDNA repairDNA sequencingmutagenesisUPD-Sequracilome

Identifiers

PMID31431505
PMCPMC6791317
OpenAlexW2969522390

What OpenQuestion holds

Textmetadata
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.