Evidence map›Paper›PMID 28245922›Full record

ArticleDevelopmental cell2017

An Hdac1/Rpd3-Poised Circuit Balances Continual Self-Renewal and Rapid Restriction of Developmental Potential during Asymmetric Stem Cell Division.

Derek H Janssens, Danielle C Hamm, Lucas Anhezini, Qi Xiao, Karsten H Siller, Sarah E Siegrist, Melissa M Harrison, Cheng-Yu Lee

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
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  5. Review
  6. Generation ofmicroPublication biology · 2025
    Article
  7. Cellular and molecular mechanisms of asymmetric stem cell division in tissue homeostasis.Genes to cells : devoted to molecular & cellular mechanisms · 2024
    Review
  8. Indirect neurogenesis in space and time.Nature reviews. Neuroscience · 2024
    Review
  9. Article
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  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
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  18. Article
  19. Fzr/Cdh1 Promotes the Differentiation of Neural Stem Cell Lineages inFrontiers in cell and developmental biology · 2020
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Derek H JanssensCellular and Molecular Biology Graduate Program, University of Michigan Medical School, Ann Arbor, MI 48109, USA; Life Sciences Institute, University of Michigan, Ann Arbor, MI 48109, USA.
Danielle C HammDepartment of Biomolecular Chemistry, University of Wisconsin - Madison, Madison, WI 53706, USA.
Lucas AnheziniLife Sciences Institute, University of Michigan, Ann Arbor, MI 48109, USA.
Qi XiaoDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Karsten H SillerAdvanced Research Computing Services, University of Virginia, Charlottesville, VA 22904, USA.
Sarah E SiegristDepartment of Biology, University of Virginia, Charlottesville, VA 22904, USA.
Melissa M HarrisonDepartment of Biomolecular Chemistry, University of Wisconsin - Madison, Madison, WI 53706, USA.
Cheng-Yu LeeCellular and Molecular Biology Graduate Program, University of Michigan Medical School, Ann Arbor, MI 48109, USA; Life Sciences Institute, University of Michigan, Ann Arbor, MI 48109, USA; Department of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI 48109, USA; Division of Molecular Medicine and Genetics, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI 48109, USA. Electronic address: leecheng@umich.edu.
University of Michigan–Ann Arbor · USUniversity of Virginia · USUniversity of Wisconsin–Madison · US

Funding

CELLULAR AND MOLECULAR BIOLOGY AT MICHIGANT32GM007315 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PUTHENVEEDU, MANOJKUMAR A · 1985 to 2021
$12.8M
Brain tumor restricts developmental potential in intermediate progenitor cellsR01NS077914 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LEE, CHENG-YU · 2012 to 2016
$1.7M
Cell growth and proliferation control in neural stem cellsR01GM120421 · NIGMS · UNIVERSITY OF VIRGINIA · PI SIEGRIST, SARAH ELIZABETH · 2016 to 2020
$1.6M
Mechanisms of genomic reprogramming and transcriptional activation in the embryoR01GM111694 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI HARRISON, MELISSA · 2015 to 2019
$1.6M
Earmuff maintains restricted potentials of mature secondary neuroblastsR01GM092818 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LEE, CHENG-YU · 2010 to 2014
$1.5M
NIGMS NIH HHS R01 GM092818NIGMS NIH HHS R01 GM111694NIGMS NIH HHS R01 GM120421NIGMS NIH HHS T32 GM007315NINDS NIH HHS R01 NS077914
6 · The paper itself

Abstract

How the developmental potential of differentiating stem cell progeny becomes rapidly and stably restricted following asymmetric stem cell division is unclear. In the fly larval brain, earmuff (erm) uniquely functions to restrict the developmental potential of intermediate neural progenitors (INPs) generated by asymmetrically dividing neural stem cells (neuroblasts). Here we demonstrate that the histone deacetylase Hdac1/Rpd3 functions together with self-renewal transcriptional repressors to maintain the erm immature INP enhancer in an inactive but poised state in neuroblasts. Within 2 hr of immature INP birth, downregulation of repressor activities alleviates Rpd3-mediated repression on the erm enhancer, enabling acetylation of multiple histone proteins and activating Erm expression. Erm restricts the developmental potential in immature INPs by repressing genes encoding neuroblast transcriptional activators. We propose that poising the fast-activating enhancers of master regulators of differentiation through continual histone deacetylation in stem cells enables self-renewal and rapid restriction of developmental potential following asymmetric division.

Indexed as

Asymmetric Cell DivisionCell Self RenewalAcetylationAnimalsBase SequenceBinding SitesCell DifferentiationConsensus SequenceDrosophila melanogasterDrosophila ProteinsEnhancer Elements, GeneticFeedback, PhysiologicalHistone Deacetylase 1Histone-Lysine N-MethyltransferaseHistonesModels, BiologicalDrosophila ProteinsHDAC1 protein, DrosophilaHistone Deacetylase 1Histone-Lysine N-MethyltransferaseHistonesPRC2 protein, DrosophilaRepressor Proteinsasymmetric stem cell divisionDrosophila brainhistone deacetylationintermediate neural progenitorsneural stem cellsneuroblastsneurogenesispoised enhancerrestricted developmental potentialself-renewal

Identifiers

PMID28245922
PMCPMC5336133
OpenAlexW2594706714

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.