Evidence map›Paper›PMID 27383233›Full record

ArticleScientific reports2016

The RNA binding protein HuR determines the differential translation of autism-associated FoxP subfamily members in the developing neocortex.

T Popovitchenko, K Thompson, B Viljetic, X Jiao, D L Kontonyiannis, M Kiledjian, R P Hart, M R Rasin

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Translational control in cortical development.Frontiers in neuroanatomy · 2022
    Article
  8. Article
  9. Article
  10. Synergistic regulation ofRNA biology · 2021
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
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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

8 authors at 2 institutions in 2 countries.

T PopovitchenkoDepartment of Neuroscience and Cell Biology, Rutgers University, Robert Wood Johnson Medical School, Piscataway 08854, NJ, USA.
K ThompsonDepartment of Neuroscience and Cell Biology, Rutgers University, Robert Wood Johnson Medical School, Piscataway 08854, NJ, USA.
B ViljeticDepartment of Neuroscience and Cell Biology, Rutgers University, Robert Wood Johnson Medical School, Piscataway 08854, NJ, USA.
X JiaoDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway 08854, NJ, USA.
D L KontonyiannisInstitute of Immunology, Biomedical Sciences Research Center Alexander Fleming, Vari, Greece.
M KiledjianDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway 08854, NJ, USA.
R P HartDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway 08854, NJ, USA.
M R RasinDepartment of Neuroscience and Cell Biology, Rutgers University, Robert Wood Johnson Medical School, Piscataway 08854, NJ, USA.
Rutgers, The State University of New Jersey · USAlexander Fleming Biomedical Sciences Research Center · GR

Funding

Regulation of Mammalian mRNA DecayR01GM067005 · NIGMS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI KILEDJIAN, MEGERDITCH · 2004 to 2022
$5.5M
Role of first neocortical RNA-Operon in specification of neocortical projection neuronsR01NS075367 · NINDS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI RASIN, MLADEN ROKO · 2011 to 2021
$3.4M
Molecular Control of Corticospinal System Formation by Intermediate TargetsR00NS064303 · NINDS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI RASIN, MLADEN ROKO · 2010 to 2012
$741k
Molecular Control of Corticospinal System Formation by Intermediate TargetsK99NS064303 · NINDS · YALE UNIVERSITY · PI RASIN, MLADEN ROKO · 2009 to 2009
$97k
NIGMS NIH HHS R01 GM067005NINDS NIH HHS K99 NS064303NINDS NIH HHS R00 NS064303NINDS NIH HHS R01 NS075367
6 · The paper itself

Abstract

Forkhead-box domain (Fox) containing family members are known to play a role in neocorticogenesis and have also been associated with disorders on the autism spectrum. Here we show that a single RNA-binding protein, Hu antigen R (HuR), dictates translation specificity of bound mRNAs and is sufficient to define distinct Foxp-characterized subpopulations of neocortical projection neurons. Furthermore, distinct phosphorylation states of HuR differentially regulate translation of Foxp mRNAs in vitro. This demonstrates the importance of RNA binding proteins within the framework of the developing brain and further confirms the role of mRNA translation in autism pathogenesis.

Indexed as

Protein Biosynthesis3' Untranslated RegionsAnimalsAutism Spectrum DisorderChromatin ImmunoprecipitationELAV-Like Protein 1FemaleForkhead Transcription FactorsGestational AgeMaleMiceNeocortexNerve Tissue ProteinsNeurogenesisPhosphorylationProtein Processing, Post-Translational3' Untranslated RegionsElavl1 protein, mouseELAV-Like Protein 1Forkhead Transcription FactorsFoxp1 protein, mouseFoxp2 protein, mouseNerve Tissue ProteinsRepressor ProteinsRNA, Messenger

Identifiers

PMID27383233
PMCPMC4935837
OpenAlexW2461964262

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.