Evidence map›Paper›PMID 26692216›Full record

ArticlePloS one2015

DNA-Binding Motif of the Imprinted Transcription Factor PEG3.

Suman Lee, An Ye, Joomyeong Kim

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. A functional outside-in signaling network of proteoglycans and matrix molecules regulating autophagy.Matrix biology : journal of the International Society for Matrix Biology · 2021
    Article
  4. Article
  5. Decorin is a devouring proteoglycan: Remodeling of intracellular catabolism via autophagy and mitophagy.Matrix biology : journal of the International Society for Matrix Biology · 2019
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Frontiers in cell and developmental biology · 2018
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. 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

3 authors at 1 institution in 1 country.

Suman LeeDepartment of Biological Sciences, Louisiana State University, Baton Rouge, Louisiana, 70803, United States of America.
An YeDepartment of Biological Sciences, Louisiana State University, Baton Rouge, Louisiana, 70803, United States of America.
Joomyeong KimDepartment of Biological Sciences, Louisiana State University, Baton Rouge, Louisiana, 70803, United States of America.
Louisiana State University · US

Funding

Imprinting studies of a paternally expressed Usp29 geneR01GM066225 · NIGMS · UNIVERSITY OF CALIF-LAWRNC LVRMR NAT LAB · PI KIM, JOOMYEONG · 2004 to 2013
$2.6M
Aebp2 as an epigenetic regulator for neural crest cellR01GM097074 · NIGMS · LOUISIANA STATE UNIV A&M COL BATON ROUGE · PI KIM, JOOMYEONG · 2013 to 2016
$1.1M
NIGMS NIH HHS R01 GM066225NIGMS NIH HHS R01-GM066225NIGMS NIH HHS R01 GM097074NIGMS NIH HHS R01-GM097074
6 · The paper itself

Abstract

Peg3 is an imprinted gene that is predicted to encode a DNA-binding zinc finger protein. This was previously demonstrated through Chromatin ImmunoPrecipitation-based Sequencing experiments. In the current study, we reanalyzed the previous ChIP-Seq results and further characterized the DNA-binding motif of PEG3. According to the results, PEG3 binds to the promoters and enhancers of a subset of genes that are closely associated with the known functions of Peg3. Some of these identified targets include Tufm, Mrpl45, Cry2, Per1, Slc25a29 and Slc38a2. With this set of targets, we derived a DNA-binding motif of PEG3, 5'-GTGGCAGT-3', which also provides a tabulated matrix that can be used for predicting other unknown genomic targets. Among the newly identified targets, we analyzed in detail the two loci, Slc38a2 and Slc38a4, which are known to be involved in neutral amino acid transport. The results indicated that PEG3 likely functions as a transcriptional repressor for these two loci. Overall, the current study provides a set of genomic targets and also redefines the DNA-binding motif for the imprinted transcription factor PEG3.

Indexed as

Amino Acid Transport System AAnimalsBinding SitesChromatin ImmunoprecipitationCryptochromesDNAGenomic ImprintingKruppel-Like Transcription FactorsMice, Inbred C57BLMitochondrial ProteinsPeptide Elongation Factor TuPeriod Circadian ProteinsTranscription FactorsAmino Acid Transport System ACry2 protein, mouseCryptochromesDNAKruppel-Like Transcription FactorsMitochondrial ProteinsPeg3 protein, mousePeptide Elongation Factor TuPer1 protein, mousePeriod Circadian ProteinsSlc38a2 protein, mouseSlc38a4 protein, mouseTranscription FactorsTufm protein, mouse

Identifiers

PMID26692216
PMCPMC4686966
OpenAlexW2407281442

What OpenQuestion holds

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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.