Evidence map›Paper›PMID 29324752›Full record

ArticlePloS one2018

Tet protein function during Drosophila development.

Fei Wang, Svetlana Minakhina, Hiep Tran, Neha Changela, Joseph Kramer, Ruth Steward

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

19 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Science advances · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. International journal of biological sciences · 2020
    Article
  15. Review
  16. Frontiers in cellular neuroscience · 2019
    Article
  17. Drosophila melanogaster as a Model System for Human Glioblastomas.Advances in experimental medicine and biology · 2019
    Review
  18. Article
  19. eNeuro
    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

6 authors at 1 institution in 2 countries.

Fei WangRutgers University, Department of Molecular Biology, Waksman Institute, Piscataway, NJ United States of America.ORCID 0000-0003-2158-3033
Svetlana MinakhinaRutgers University, Department of Molecular Biology, Waksman Institute, Piscataway, NJ United States of America.ORCID 0000-0002-3879-7751
Hiep TranRutgers University, Department of Molecular Biology, Waksman Institute, Piscataway, NJ United States of America.ORCID 0000-0001-5312-8989
Neha ChangelaRutgers University, Department of Molecular Biology, Waksman Institute, Piscataway, NJ United States of America.
Joseph KramerRutgers University, Department of Molecular Biology, Waksman Institute, Piscataway, NJ United States of America.
Ruth StewardRutgers University, Department of Molecular Biology, Waksman Institute, Piscataway, NJ United States of America.
Rutgers, The State University of New Jersey · US

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
RNA processing in Drosophila developmentR01GM120405 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI STEWARD, RUTH M · 2016 to 2019
$1.2M
Cell proliferation in hematopoiesisR01GM089992 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI STEWARD, RUTH M · 2010 to 2013
$1.1M
NIGMS NIH HHS R01 GM089992NIGMS NIH HHS R01 GM120405NIH HHS 1 R01 GM120405-01NIH HHS 2R01 GM089992NIH HHS P40 OD018537
6 · The paper itself

Abstract

The TET (Ten-eleven translocation) 1, 2 and 3 proteins have been shown to function as DNA hydroxymethylases in vertebrates and their requirements have been documented extensively. Recently, the Tet proteins have been shown to also hydroxylate 5-methylcytosine in RNA. 5-hydroxymethylcytosine (5hmrC) is enriched in messenger RNA but the function of this modification has yet to be elucidated. Because Cytosine methylation in DNA is barely detectable in Drosophila, it serves as an ideal model to study the biological function of 5hmrC. Here, we characterized the temporal and spatial expression and requirement of Tet throughout Drosophila development. We show that Tet is essential for viability as Tet complete loss-of-function animals die at the late pupal stage. Tet is highly expressed in neuronal tissues and at more moderate levels in somatic muscle precursors in embryos and larvae. Depletion of Tet in muscle precursors at early embryonic stages leads to defects in larval locomotion and late pupal lethality. Although Tet knock-down in neuronal tissue does not cause lethality, it is essential for neuronal function during development through its affects upon locomotion in larvae and the circadian rhythm of adult flies. Further, we report the function of Tet in ovarian morphogenesis. Together, our findings provide basic insights into the biological function of Tet in Drosophila, and may illuminate observed neuronal and muscle phenotypes observed in vertebrates.

Indexed as

AnimalsCircadian RhythmDNA-Binding ProteinsDNA MethylationDrosophilaFemaleLocomotionMusclesNeuronsOvaryDNA-Binding Proteins

Identifiers

PMID29324752
PMCPMC5764297
OpenAlexW2783378156

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.