Evidence map›Paper›PMID 25350849›Full record

ArticlePloS one2014

Olig3 is not involved in the ventral patterning of spinal cord.

Zijing Liu, Xuemei Hu, Chengcheng Huang, Kang Zheng, Hirohide Takebayashi, Cheng Cao, Mengsheng Qiu

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. 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

7 authors at 3 institutions in 3 countries.

Zijing LiuDepartment of Anatomical Sciences and Neurobiology, University of Louisville, Louisville, KY, United States of America; Beijing Institute of Biotechnology, Beijing, PR China.
Xuemei HuDepartment of Anatomical Sciences and Neurobiology, University of Louisville, Louisville, KY, United States of America.
Chengcheng HuangBeijing Institute of Biotechnology, Beijing, PR China.
Kang ZhengInstitute of Developmental and Regenerative Biology, Zhejiang Key Laboratory of Organ Development and Regeneration, Hangzhou Normal University, Hangzhou, PR China.
Hirohide TakebayashiDivision of Neurobiology and Anatomy, Graduate School of Medical and Dental Sciences, Niigata University, Niigata, Japan.
Cheng CaoBeijing Institute of Biotechnology, Beijing, PR China.
Mengsheng QiuDepartment of Anatomical Sciences and Neurobiology, University of Louisville, Louisville, KY, United States of America; Institute of Developmental and Regenerative Biology, Zhejiang Key Laboratory of Organ Development and Regeneration, Hangzhou Normal University, Hangzhou, PR China.
Hangzhou Normal University · CNUniversity of Louisville · USNiigata University · JP

Funding

Transcriptional control of oligodendrocyte differentiation and myelinationR01NS037717 · NINDS · UNIVERSITY OF LOUISVILLE · PI QIU, MENGSHENG · 2000 to 2013
$3.6M
NINDS NIH HHS R01 NS037717
6 · The paper itself

Abstract

At embryonic stages, Olig3 is initially expressed in the dorsal-most region of the spinal cord, but later in the ventral marginal zone as well. Previous studies indicated that Olig3 controlled the patterning of dorsal spinal cord and loss of Olig3 function led to the re-specification of dI2 and dI3 neurons into dI4 interneurons. However, the role of Olig3 in regulating the development of ventral spinal cord has remained unknown. BrdU labeling demonstrated that ventral Olig3 was expressed in the post-mitotic neurons and Olig3+ cells seen at late embryonic stages were born at the earlier stage but remained in the marginal zone throughout embryogenesis. Loss-of-function and gain-of-function experiment indicated that Nkx2.2 regulated the expression of Olig3 in V3 interneurons. However, Olig3 mutation didn't apparently affect the generation and migration of ventral neurons. These findings suggest that Olig3 plays different roles in regulating the development of dorsal and ventral spinal cord.

Indexed as

Body PatterningGene Expression Regulation, DevelopmentalAnimalsBasic Helix-Loop-Helix ProteinsCell CountCell DifferentiationChick EmbryoElectroporationGenotypeHomeobox Protein Nkx-2.2Homeodomain ProteinsInterneuronsMiceMitosisMutationNeuronsBasic Helix-Loop-Helix ProteinsHomeobox Protein Nkx-2.2Homeodomain Proteinsnkx2.2b protein, zebrafishNkx2-2 protein, mouseOlig3 protein, mouseTranscription FactorsZebrafish Proteins

Identifiers

PMID25350849
PMCPMC4211884
OpenAlexW2079152431

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.