Evidence map›Paper›PMID 24599466›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Prenatal deletion of the RNA-binding protein HuD disrupts postnatal cortical circuit maturation and behavior.

Erik M DeBoer, Ricardo Azevedo, Taylor A Vega, Jesse Brodkin, Wado Akamatsu, Hideyuki Okano, George C Wagner, Mladen-Roko Rasin

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

46 citing papers in PubMed, 73 citations in OpenAlex.

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  7. The molecular genetics of nELAVL in brain development and disease.European journal of human genetics : EJHG · 2023
    Review
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  19. RNA Modifications and RNA Metabolism in Neurological Disease Pathogenesis.International journal of molecular sciences · 2021
    Review
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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 4 institutions in 2 countries.

Erik M DeBoerDepartment of Neuroscience and Cell Biology, Robert Wood Johnson Medical School and Department of Psychology, Rutgers University, Piscataway, New Jersey 08854, University of California, Berkeley, California 94704, Behavioral Instruments, Hillsborough, New Jersey 08854, and Department of Physiology, Keio University, Tokyo 160-8582, Japan.
Ricardo Azevedo
Taylor A Vega
Jesse Brodkin
Wado Akamatsu
Hideyuki Okano
George C Wagner
Mladen-Roko Rasin
Johnson University · USKeio University · JPRutgers, The State University of New Jersey · USUniversity of California, Berkeley · US

Funding

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
NINDS NIH HHS K99 NS064303NINDS NIH HHS NS064303NINDS NIH HHS NS075367NINDS NIH HHS R00 NS064303NINDS NIH HHS R01 NS075367
6 · The paper itself

Abstract

The proper functions of cortical circuits are dependent upon both appropriate neuronal subtype specification and their maturation to receive appropriate signaling. These events establish a balanced circuit that is important for learning, memory, emotion, and complex motor behaviors. Recent research points to mRNA metabolism as a key regulator of this development and maturation process. Hu antigen D (HuD), an RNA-binding protein, has been implicated in the establishment of neuronal identity and neurite outgrowth in vitro. Therefore, we investigated the role of HuD loss of function on neuron specification and dendritogenesis in vivo using a mouse model. We found that loss of HuD early in development results in a defective early dendritic overgrowth phase and pervasive deficits in neuron specification in the lower neocortical layers and defects in dendritogenesis in the CA3 region of the hippocampus. Subsequent behavioral analysis revealed a deficit in performance of a hippocampus-dependent task: the Morris water maze. Further, HuD knock-out (KO) mice exhibited lower levels of anxiety than their wild-type counterparts and were overall less active. Last, we found that HuD KO mice are more susceptible to auditory-induced seizures, often resulting in death. Our findings suggest that HuD is necessary for the establishment of neocortical and hippocampal circuitry and is critical for their function.

Indexed as

AnimalsAnimals, NewbornELAV-Like Protein 4ELAV ProteinsFemaleGene DeletionHippocampusMaleMaze LearningMiceMice, KnockoutNeocortexNerve NetRNA-Binding ProteinsSeizuresElavl4 protein, mouseELAV-Like Protein 4ELAV ProteinsRNA-Binding Proteins

Identifiers

PMID24599466
PMCPMC3942583
OpenAlexW1990508004

What OpenQuestion holds

Textmetadata
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.