Evidence map›Paper›PMID 28665982›Full record

ArticlePloS one2017

The SERTAD protein Taranis plays a role in Polycomb-mediated gene repression.

Pranabananda Dutta, Willis X Li

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. TARANIS Interacts with VRILLE and PDP1 to Modulate the Circadian Transcriptional Feedback Mechanism inThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  3. Article
  4. Drosophila SERTAD domain protein Taranis is required in somatic cells for maintenance of male germline stem cells.Developmental dynamics : an official publication of the American Association of Anatomists · 2021
    Article
  5. 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

2 authors at 2 institutions in 1 country.

Pranabananda DuttaDepartment of Medicine, University of California San Diego, La Jolla, California, United States of America.
Willis X LiDepartment of Medicine, University of California San Diego, La Jolla, California, United States of America.
University of California, San Diego · USUniversity of Rochester Medical Center · US

Funding

Epigenetic tumor induction by heterochromatin instabilityR01CA131326 · NCI · UNIVERSITY OF ROCHESTER · PI LI, WILLIS X · 2009 to 2013
$1.3M
Unphosphorylated STAT recruits HP1 for gene repressionR03CA212727 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LI, WILLIS X · 2017 to 2018
$155k
NCI NIH HHS R01 CA131326NCI NIH HHS R03 CA212727
6 · The paper itself

Abstract

The Polycomb group (PcG) proteins have been implicated in epigenetic transcriptional repression in development, stem cell maintenance and in cancer. The chromodomain protein Polycomb (Pc) is a key member of the PcG. Pc binds to the histone mark, trimethylated histone 3 lysine 27 (H3K27me3), to initiate transcriptional repression. How PcG proteins are recruited to target loci is not fully understood. Here we show that the Drosophila SERTA domain protein Taranis (Tara) is involved in transcriptional regulation of Pc target genes. Embryos lacking Tara exhibit a partial homeotic transformation of cuticular the segments, a phenotype associated with the loss of Pc function. Moreover, Drosophila embryos homozygous for a tara hypomorphic allele also misexpress engrailed, a Pc-regulated gene, and this phenotype is associated with the loss of Pc binding to the cis response element in the engrailed enhancer. In relation to that, Pc recruitment is reduced on the salivary gland polytene chromosomes and specifically at the engrailed locus. These results suggest that Tara might be required for positioning Pc to a subset of its target genes.

Indexed as

AnimalsCell Cycle ProteinsChromatin ImmunoprecipitationDrosophila melanogasterDrosophila ProteinsGene Expression RegulationIn Situ Hybridization, FluorescencePolycomb-Group ProteinsTranscription, GeneticTransgenesCell Cycle ProteinsDrosophila ProteinsPolycomb-Group Proteinstara protein, Drosophila

Identifiers

PMID28665982
PMCPMC5493352
OpenAlexW2726965062

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.