Evidence map›Paper›PMID 25568339›Full record

ArticleMolecular biology of the cell2015

Misexpression of BRE gene in the developing chick neural tube affects neurulation and somitogenesis.

Guang Wang, Yan Li, Xiao-Yu Wang, Manli Chuai, John Yeuk-Hon Chan, Jian Lei, Andrea Münsterberg, Kenneth Ka Ho Lee, Xuesong Yang

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Mycotoxin Fumonisin BToxins · 2021
    Article
  4. Article
  5. Article
  6. Article
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 4 institutions in 2 countries.

Guang WangDepartment of Histology and Embryology, School of Medicine, Key Laboratory for Regenerative Medicine of the Ministry of Education, Jinan University, Guangzhou 510632, China.
Yan LiDepartment of Histology and Embryology, School of Medicine, Key Laboratory for Regenerative Medicine of the Ministry of Education, Jinan University, Guangzhou 510632, China.
Xiao-Yu WangDepartment of Histology and Embryology, School of Medicine, Key Laboratory for Regenerative Medicine of the Ministry of Education, Jinan University, Guangzhou 510632, China.
Manli ChuaiDivision of Cell and Developmental Biology, University of Dundee, Dundee DD1 5EH, United Kingdom.
John Yeuk-Hon ChanDepartment of Histology and Embryology, School of Medicine, Key Laboratory for Regenerative Medicine of the Ministry of Education, Jinan University, Guangzhou 510632, China.
Jian LeiDepartment of Histology and Embryology, School of Medicine, Key Laboratory for Regenerative Medicine of the Ministry of Education, Jinan University, Guangzhou 510632, China.
Andrea MünsterbergSchool of Biological Sciences, University of East Anglia, Norwich NR4 7TJ, United Kingdom.
Kenneth Ka Ho LeeKey Laboratory for Regenerative Medicine of the Ministry of Education, School of Biomedical Sciences, Chinese University of Hong Kong, Shatin, Hong Kong.
Xuesong YangDepartment of Histology and Embryology, School of Medicine, Key Laboratory for Regenerative Medicine of the Ministry of Education, Jinan University, Guangzhou 510632, China yang_xuesong@126.com kaholee@cuhk.edu.hk.
Jinan University · CNChinese University of Hong Kong · CNUniversity of Dundee · GBUniversity of East Anglia · GB

Funding

British Heart Foundation PG/11/118/29292
6 · The paper itself

Abstract

The brain and reproductive expression (BRE) gene is expressed in numerous adult tissues and especially in the nervous and reproductive systems. However, little is known about BRE expression in the developing embryo or about its role in embryonic development. In this study, we used in situ hybridization to reveal the spatiotemporal expression pattern for BRE in chick embryo during development. To determine the importance of BRE in neurogenesis, we overexpressed BRE and also silenced BRE expression specifically in the neural tube. We established that overexpressing BRE in the neural tube indirectly accelerated Pax7(+) somite development and directly increased HNK-1(+) neural crest cell (NCC) migration and TuJ-1(+) neurite outgrowth. These altered morphogenetic processes were associated with changes in the cell cycle of NCCs and neural tube cells. The inverse effect was obtained when BRE expression was silenced in the neural tube. We also determined that BMP4 and Shh expression in the neural tube was affected by misexpression of BRE. This provides a possible mechanism for how altering BRE expression was able to affect somitogenesis, neurogenesis, and NCC migration. In summary, our results demonstrate that BRE plays an important role in regulating neurogenesis and indirectly somite differentiation during early chick embryo development.

Indexed as

AnimalsBone Morphogenetic Protein 4Cell MovementChick EmbryoGene Expression Regulation, DevelopmentalHedgehog ProteinsNerve Tissue ProteinsNeural CrestNeural TubeNeurulationPAX7 Transcription FactorSomitesBone Morphogenetic Protein 4Hedgehog ProteinsNerve Tissue ProteinsPAX7 Transcription Factor

Identifiers

PMID25568339
PMCPMC4342032
OpenAlexW2096363596

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.