Evidence map›Paper›PMID 29033307›Full record

ArticleStem cell reports2017

NEUROG1 Regulates CDK2 to Promote Proliferation in Otic Progenitors.

Zhichao Song, Azadeh Jadali, Bernd Fritzsch, Kelvin Y Kwan

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

Zhichao SongDepartment of Cell Biology & Neuroscience, Rutgers University, Piscataway, NJ 08854, USA; Stem Cell Research Center and Keck Center for Collaborative Neuroscience, Rutgers University, Piscataway, NJ 08854, USA.
Azadeh JadaliDepartment of Cell Biology & Neuroscience, Rutgers University, Piscataway, NJ 08854, USA; Stem Cell Research Center and Keck Center for Collaborative Neuroscience, Rutgers University, Piscataway, NJ 08854, USA.
Bernd FritzschDepartment of Biology, University of Iowa, CLAS, 214 BB, Iowa City, IA 52242, USA.
Kelvin Y KwanDepartment of Cell Biology & Neuroscience, Rutgers University, Piscataway, NJ 08854, USA; Stem Cell Research Center and Keck Center for Collaborative Neuroscience, Rutgers University, Piscataway, NJ 08854, USA. Electronic address: kwan@dls.rutgers.edu.
Rutgers, The State University of New Jersey · USUniversity of Iowa · US

Funding

The role of transcription factors and chromatin remodeling proteins in spiral ganglion neuron regenerationR01DC015000 · NIDCD · RUTGERS, THE STATE UNIV OF N.J. · PI KWAN, KELVIN Y. · 2016 to 2020
$2.0M
NIDCD NIH HHS R01 DC015000
6 · The paper itself

Abstract

Loss of spiral ganglion neurons (SGNs) significantly contributes to hearing loss. Otic progenitor cell transplantation is a potential strategy to replace lost SGNs. Understanding how key transcription factors promote SGN differentiation in otic progenitors accelerates efforts for replacement therapies. A pro-neural transcription factor, Neurogenin1 (Neurog1), is essential for SGN development. Using an immortalized multipotent otic progenitor (iMOP) cell line that can self-renew and differentiate into otic neurons, NEUROG1 was enriched at the promoter of cyclin-dependent kinase 2 (Cdk2) and neurogenic differentiation 1 (NeuroD1) genes. Changes in H3K9ac and H3K9me3 deposition at the Cdk2 and NeuroD1 promoters suggested epigenetic regulation during iMOP proliferation and differentiation. In self-renewing iMOP cells, overexpression of NEUROG1 increased CDK2 to drive proliferation, while knockdown of NEUROG1 decreased CDK2 and reduced proliferation. In iMOP-derived neurons, overexpression of NEUROG1 accelerated acquisition of neuronal morphology, while knockdown of NEUROG1 prevented differentiation. Our findings suggest that NEUROG1 can promote proliferation or neuronal differentiation.

Indexed as

Cell ProliferationNeurogenesisAnimalsBasic Helix-Loop-Helix ProteinsCells, CulturedCyclin-Dependent Kinase 2Histone CodeMiceNerve Tissue ProteinsNeural Stem CellsSpiral GanglionBasic Helix-Loop-Helix ProteinsCdk2 protein, mouseCyclin-Dependent Kinase 2Nerve Tissue ProteinsNeurod1 protein, mouseNeurog1 protein, mouseauditorychromatinepigeneticsiMOPinner earneurogeninprogenitorspiral ganglion neurons

Identifiers

PMID29033307
PMCPMC5829327
OpenAlexW2761450544

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.