Evidence map›Paper›PMID 30306660›Full record

ArticleGlia2018

NG2 expression in NG2 glia is regulated by binding of SoxE and bHLH transcription factors to a Cspg4 intronic enhancer.

Hitoshi Gotoh, William M Wood, Kiran D Patel, Daniel C Factor, Linda L Boshans, Tadashi Nomura, Paul J Tesar, Katsuhiko Ono, Akiko Nishiyama

Abstract read
In one paragraph

Article in Glia, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
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  9. Article
  10. Life-long oligodendrocyte development and plasticity.Seminars in cell & developmental biology · 2021
    Article
  11. Article
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  15. Review
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

9 authors at 3 institutions in 2 countries.

Hitoshi GotohDepartment of Physiology and Neurobiology, University of Connecticut, Storrs, Connecticut.
William M WoodDepartment of Physiology and Neurobiology, University of Connecticut, Storrs, Connecticut.
Kiran D PatelDepartment of Physiology and Neurobiology, University of Connecticut, Storrs, Connecticut.
Daniel C FactorDepartment of Genetics and Genome Sciences, Case Western Reserve University School of Medicine, Cleveland, Ohio.
Linda L BoshansDepartment of Physiology and Neurobiology, University of Connecticut, Storrs, Connecticut.
Tadashi NomuraDepartment of Biology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Paul J TesarDepartment of Genetics and Genome Sciences, Case Western Reserve University School of Medicine, Cleveland, Ohio.
Katsuhiko OnoDepartment of Biology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Akiko NishiyamaDepartment of Physiology and Neurobiology, University of Connecticut, Storrs, Connecticut.ORCID 0000-0001-7252-0812
University of Connecticut · USKyoto Prefectural University · JPUniversity School · US

Funding

Inflammation and NG2 Cell DifferentiationR01NS073425 · NINDS · UNIVERSITY OF CONNECTICUT STORRS · PI NISHIYAMA, AKIKO · 2011 to 2021
$3.3M
Heterogeneity of NG2 Glial CellsR01NS074870 · NINDS · UNIVERSITY OF CONNECTICUT STORRS · PI NISHIYAMA, AKIKO · 2012 to 2016
$1.7M
NIH HHS R01 NS073425NIH HHS R01 NS074870NINDS NIH HHS R01 NS073425NINDS NIH HHS R01 NS074870
6 · The paper itself

Abstract

NG2 is a type 1 integral membrane glycoprotein encoded by the Cspg4 gene. It is expressed on glial progenitor cells known as NG2 glial cells or oligodendrocyte precursor cells that exist widely throughout the developing and mature central nervous system and vascular mural cells but not on mature oligodendrocytes, astrocytes, microglia, neurons, or neural stem cells. Hence NG2 is widely used as a marker for NG2 glia in the rodent and human. The regulatory elements of the mouse Cspg4 gene and its flanking sequences have been used successfully to target reporter and Cre recombinase to NG2 glia in transgenic mice when used in a large 200 kb bacterial artificial chromosome cassette containing the 38 kb Cspg4 gene in the center. Despite the tightly regulated cell type- and stage-specific expression of NG2 in the brain and spinal cord, the mechanisms that regulate its transcription have remained unknown. Here, we describe a 1.45 kb intronic enhancer of the mouse Cspg4 gene that directed transcription of EGFP reporter to NG2 glia but not to pericytes in vitro and in transgenic mice. The 1.45 kb enhancer contained binding sites for SoxE and basic helix-loop-helix transcription factors, and its enhancer activity was augmented cooperatively by these factors, whose respective binding elements were found in close proximity to each other. Mutations in these binding elements abrogated the enhancer activity when tested in the postnatal mouse brain.

Indexed as

Age FactorsAnimalsAnimals, NewbornAntigensBasic Helix-Loop-Helix ProteinsBinding SitesBrainChondroitin Sulfate Proteoglycan 4Chromatin ImmunoprecipitationEnhancer Elements, GeneticGene Expression Regulation, DevelopmentalGlial Fibrillary Acidic ProteinGreen Fluorescent ProteinsHistonesMiceMice, Inbred ICRAntigensBasic Helix-Loop-Helix ProteinsChondroitin Sulfate Proteoglycan 4enhanced green fluorescent proteinGlial Fibrillary Acidic ProteinGreen Fluorescent ProteinsHistonesOlig2 protein, mouseOligodendrocyte Transcription Factor 2ProteoglycansSox10 protein, mouseSOXE Transcription FactorsAscl1Cspg4NG2Olig2oligodendrocyte precursor cellSox10

Identifiers

PMID30306660
PMCPMC6309483
OpenAlexW2898071764

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.