Evidence map›Paper›PMID 25064607›Full record

ArticleMolecular and biochemical parasitology2014

Tb927.10.6900 encodes the glucosyltransferase involved in synthesis of base J in Trypanosoma brucei.

Aarthi Sekar, Christopher Merritt, Loren Baugh, Kenneth Stuart, Peter J Myler

Abstract read
In one paragraph

Article in Molecular and biochemical parasitology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Characterization and structure determination of a llama-derived nanobody targeting the J-base binding protein 1.Acta crystallographica. Section F, Structural biology communications · 2018
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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

5 authors.

Aarthi SekarSeattle Biomedical Research Institute, 307 Westlake Avenue N., Seattle WA 98109-5219, USA.
Christopher MerrittSeattle Biomedical Research Institute, 307 Westlake Avenue N., Seattle WA 98109-5219, USA.
Loren BaughSeattle Biomedical Research Institute, 307 Westlake Avenue N., Seattle WA 98109-5219, USA.
Kenneth StuartSeattle Biomedical Research Institute, 307 Westlake Avenue N., Seattle WA 98109-5219, USA; Department of Global Health, University of Washington, Seattle, WA 98195, USA.
Peter J MylerSeattle Biomedical Research Institute, 307 Westlake Avenue N., Seattle WA 98109-5219, USA; Department of Biomedical Informatics & Medical Education, Seattle, WA 98195, USA; Department of Global Health, University of Washington, Seattle, WA 98195, USA. Electronic address: peter.myler@seattlebiomed.org.

Funding

Base J and transcription termination in LeishmaniaR01AI103858 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI MYLER, PETER JOHN · 2013 to 2017
$2.8M
NIAID NIH HHS 1R01AI103858NIAID NIH HHS R01 AI103858
6 · The paper itself

Abstract

Base J is a DNA modification found in the genome of Trypanosoma brucei and all other kinetoplastids analyzed, where it replaces a small fraction of Ts, mainly in telomeric and chromosome-internal transcription initiation and termination regions. The synthesis of base J is a two-step process whereby a specific T is converted to HOMedU (hydroxymethyldeoxyuridine) and subsequently glucosylated to generate J. The thymidine hydroxylases (JPB1 and JBP2) that catalyze the first step have been characterized, but the identity of the glucosyltransferase catalyzing the second step has proven elusive. Recent bioinformatic analysis by Iyer et al. (Nucleic Acids Res 2013;41:7635) suggested that Tb927.10.6900 encodes the glucosyltransferase (HmdUGT) responsible for converting HOMedU to J in T. brucei. We now present experimental evidence to validate this hypothesis; null mutants of Tb927.10.6900 are unable to synthesize base J. Orthologues from related kinetoplastids show only modest conservation, with several insertion sequences found in those from Leishmania and related genera.

Indexed as

Gene DeletionGlucosyltransferasesMetabolic Networks and PathwaysThymineTrypanosoma brucei bruceiGlucosyltransferasesThymineDNA modificationEpigeneticsGlucosyltransferaseTranscriptional read-throughTrypanosomatids

Identifiers

PMID25064607
PMCPMC4206709

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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.