Evidence map›Paper›PMID 20969844›Full record

ArticleDevelopmental biology2011

Neuronal transcriptional repressor REST suppresses an Atoh7-independent program for initiating retinal ganglion cell development.

Chai-An Mao, Wen-Wei Tsai, Jang-Hyeon Cho, Ping Pan, Michelle Craig Barton, William H Klein

Abstract read
In one paragraph

Article in Developmental biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. On the Generation and Regeneration of Retinal Ganglion Cells.Frontiers in cell and developmental biology · 2020
    Article
  7. Article
  8. Article
  9. Article
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  11. Article
  12. Novel Regulatory Mechanisms for the SoxC Transcriptional Network Required for Visual Pathway Development.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  13. Article
  14. The Importance of REST for Development and Function of Beta Cells.Frontiers in cell and developmental biology · 2017
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

6 authors at 1 institution in 1 country.

Chai-An MaoDepartment of Biochemistry and Molecular Biology, The University of Texas M. D. Anderson Cancer Center, Houston, TX, 77030, USA. cmao@mdanderson.org
Wen-Wei Tsai
Jang-Hyeon Cho
Ping Pan
Michelle Craig Barton
William H Klein
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
The Role of p53 in Human Embryonic Stem CellsP01GM081627 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI SONGYANG, ZHOU · 2007 to 2011
$9.9M
VISION RESEARCHP30EY010608 · NEI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MASSEY, STEPHEN C · 1994 to 2014
$7.9M
Optic nerve regeneration: gene networks in retina developmentR01EY011930 · NEI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KLEIN, WILLIAM H. · 1997 to 2016
$5.3M
NCI NIH HHS CA016672NCI NIH HHS P30 CA016672NEI NIH HHS EY010608-139005NEI NIH HHS EY011930NEI NIH HHS R01 EY011930NIGMS NIH HHS GM081627NIGMS NIH HHS P01 GM081627
6 · The paper itself

Abstract

As neuronal progenitors differentiate into neurons, they acquire a unique set of transcription factors. The transcriptional repressor REST prevents progenitors from undergoing differentiation. Notably, REST binding sites are often associated with retinal ganglion cell (RGC) genes whose expression in the retina is positively controlled by Atoh7, a factor essential for RGC formation. The key regulators that enable a retinal progenitor cell (RPC) to commit to an RGC fate have not been identified. We show here that REST suppresses RGC gene expression in RPCs. REST inactivation causes aberrant expression of RGC transcription factors in proliferating RPCs, independent of Atoh7, resulting in increased RGC formation. Strikingly, inactivating REST in Atoh7-null retinas restores transcription factor expression, which partially activates downstream RGC genes but is insufficient to prevent RGC loss. Our results demonstrate an Atoh7-independent program for initial activation of RGC genes and suggest a novel role for REST in preventing premature expression in RPCs.

Indexed as

Cell DifferentiationGene Expression Regulation, DevelopmentalAnimalsBase SequenceBasic Helix-Loop-Helix ProteinsFemaleHomeodomain ProteinsMaleMiceMice, Inbred C57BLMutationNerve Tissue ProteinsProtein BindingRE1-Silencing Transcription FactorRepressor ProteinsRetinal Ganglion CellsAtoh7 protein, mouseBasic Helix-Loop-Helix ProteinsHomeodomain ProteinsNerve Tissue ProteinsPou4f2 protein, mouseRE1-Silencing Transcription FactorRepressor ProteinsTranscription Factor Brn-3B

Identifiers

PMID20969844
PMCPMC2993882
OpenAlexW2075926073

What OpenQuestion holds

Textmetadata
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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.