Evidence map›Paper›PMID 27050508›Full record

ArticleCell reports2016

Type I bHLH Proteins Daughterless and Tcf4 Restrict Neurite Branching and Synapse Formation by Repressing Neurexin in Postmitotic Neurons.

Mitchell D'Rozario, Ting Zhang, Edward A Waddell, Yonggang Zhang, Cem Sahin, Michal Sharoni, Tina Hu, Mohammad Nayal, Kaveesh Kutty, Faith Liebl and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
12.3field-weighted citation impact, top 2% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
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  17. Neurexins cluster CaThe EMBO journal · 2020
    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

12 authors at 3 institutions in 1 country.

Mitchell D'RozarioDepartment of Biology, Drexel University, Philadelphia, PA 19104, USA.
Ting ZhangDepartment of Neuroscience, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Edward A WaddellDepartment of Biology, Drexel University, Philadelphia, PA 19104, USA.
Yonggang ZhangDepartment of Neuroscience, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Cem SahinDepartment of Electrical and Computer Engineering, Drexel University, Philadelphia, PA 19104, USA.
Michal SharoniDepartment of Biology, Drexel University, Philadelphia, PA 19104, USA.
Tina HuDepartment of Biology, Drexel University, Philadelphia, PA 19104, USA.
Mohammad NayalDepartment of Biology, Drexel University, Philadelphia, PA 19104, USA.
Kaveesh KuttyDepartment of Biology, Drexel University, Philadelphia, PA 19104, USA.
Faith LieblDepartment of Biological Sciences, Southern Illinois University Edwardsville, Edwardsville, IL 62026, USA.
Wenhui HuDepartment of Neuroscience, Temple University School of Medicine, Philadelphia, PA 19140, USA. Electronic address: whu@temple.edu.
Daniel R MarendaDepartment of Biology, Drexel University, Philadelphia, PA 19104, USA; Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA 19104, USA. Electronic address: daniel.marenda@drexel.edu.
Drexel University · USTemple University · USSouthern Illinois University Edwardsville · US

Funding

Role and mechanism of NIBP/NFkB signaling in neurogenesisR01MH101041 · NIMH · TEMPLE UNIV OF THE COMMONWEALTH · PI HU, WENHUI · 2013 to 2015
$594k
NIMH NIH HHS R01 MH101041NIMH NIH HHS R01MH101041
6 · The paper itself

Abstract

Proneural proteins of the class I/II basic-helix-loop-helix (bHLH) family are highly conserved transcription factors. Class I bHLH proteins are expressed in a broad number of tissues during development, whereas class II bHLH protein expression is more tissue restricted. Our understanding of the function of class I/II bHLH transcription factors in both invertebrate and vertebrate neurobiology is largely focused on their function as regulators of neurogenesis. Here, we show that the class I bHLH proteins Daughterless and Tcf4 are expressed in postmitotic neurons in Drosophila melanogaster and mice, respectively, where they function to restrict neurite branching and synapse formation. Our data indicate that Daughterless performs this function in part by restricting the expression of the cell adhesion molecule Neurexin. This suggests a role for these proteins outside of their established roles in neurogenesis.

Indexed as

MitosisAnimalsAxonsBasic Helix-Loop-Helix ProteinsBehavior, AnimalCell Adhesion Molecules, NeuronalCell DifferentiationDrosophila melanogasterDrosophila ProteinsGene Knockdown TechniquesMiceMotor ActivityNeuritesNeuromuscular JunctionPhenotypePresynaptic TerminalsBasic Helix-Loop-Helix ProteinsCell Adhesion Molecules, NeuronalDa protein, DrosophilaDrosophila ProteinsNrx protein, DrosophilaTcf4 protein, DrosophilabHLHdaughterlessNMJPitt-HopkinsproneuralschizophreniaTCF4

Identifiers

PMID27050508
PMCPMC4946342
OpenAlexW2314150394

What OpenQuestion holds

Textmetadata
LicenceTDM
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.