Evidence map›Paper›PMID 10954611›Full record

ArticleNucleic acids research2000

REST-VP16 activates multiple neuronal differentiation genes in human NT2 cells.

A Immaneni, P Lawinger, Z Zhao, W Lu, L Rastelli, J H Morris, S Majumder

Open access · greenAbstract read
In one paragraph

Article in Nucleic acids research, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
0.6field-weighted citation impact, top 27% 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

25 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
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  5. Review
  6. Review
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  8. Article
  9. Regulation of neural gene transcription by optogenetic inhibition of the RE1-silencing transcription factor.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  10. Article
  11. Article
  12. Article
  13. The master negative regulator REST/NRSF controls adult neurogenesis by restraining the neurogenic program in quiescent stem cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    Article
  14. The RE1 binding protein REST regulates oligodendrocyte differentiation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    Article
  15. Article
  16. Article
  17. 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

7 authors at 1 institution in 1 country.

A ImmaneniUniversity of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Box 316, Houston, TX 77030, USA.
P Lawinger
Z Zhao
W Lu
L Rastelli
J H Morris
S Majumder
The University of Texas MD Anderson Cancer Center · US

Funding

TRANSCRIPTION FACTOR REST/NRSF IN MEDULLOBLASTOMAR01CA081255 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MAJUMDER, SADHAN · 1999 to 2010
$2.1M
MECHANISM OF ENHANCER FUNCTION IN MOUSE EMBRYOS/OCCYTESR01GM053454 · NIGMS · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI MAJUMDER, SADHAN · 1996 to 2000
$169k
NCI NIH HHS CA81255NCI NIH HHS R01 CA081255NIGMS NIH HHS GM53454
6 · The paper itself

Abstract

The RE1-silencing transcription factor (REST)/neuron-restrictive silencer factor (NRSF) can repress transcription of a battery of neuronal differentiation genes in non-neuronal cells by binding to a specific consensus DNA sequence present in their regulatory regions. However, REST/NRSF(-/-) mice suggest that the absence of REST/NRSF-dependent repression alone is not sufficient for the expression of these neuronal differentiation genes and that the presence of other promoter/enhancer-specific activators is required. Here we describe the construction of a recombinant transcription factor, REST-VP16, by replacing repressor domains of REST/NRSF with the activation domain of a viral activator VP16. In transient transfection experiments, REST-VP16 was found to operate through RE1 binding site/neuron-restrictive enhancer element (RE1/NRSE), activate plasmid-encoded neuronal promoters in various mammalian cell types and activate cellular REST/NRSF target genes, even in the absence of factors that are otherwise required to activate such genes. Efficient expression of REST-VP16 through adenoviral vectors in NT2 cells, which resemble human committed neuronal progenitor cells, was found to cause activation of multiple neuronal genes that are characteristic markers for neuronal differentiation. Thus, REST-VP16 could be used as a unique tool to study neuronal differentiation pathways and neuronal diseases that arise due to the deregulation of this process.

Indexed as

Cell DifferentiationAdenoviridaeAntigens, DifferentiationGene SilencingHerpes Simplex Virus Protein Vmw65HumansNeuronsPlasmidsProtein Structure, TertiaryRE1-Silencing Transcription FactorRecombinant Fusion ProteinsRepressor ProteinsResponse ElementsRNA, MessengerStem CellsTATA BoxAntigens, DifferentiationHerpes Simplex Virus Protein Vmw65RE1-Silencing Transcription FactorRecombinant Fusion ProteinsRepressor ProteinsRNA, MessengerTranscription Factors

Identifiers

PMID10954611
PMCPMC110685
OpenAlexW2157782117

What OpenQuestion holds

Textmetadata
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.