Evidence map›Paper›PMID 22745313›Full record

ArticleDevelopment (Cambridge, England)2012

klumpfuss distinguishes stem cells from progenitor cells during asymmetric neuroblast division.

Qi Xiao, Hideyuki Komori, Cheng-Yu Lee

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

49 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
  2. Article
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  11. Indirect neurogenesis in space and time.Nature reviews. Neuroscience · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

3 authors at 1 institution in 1 country.

Qi XiaoDepartment of Cell and Developmental Biology, Life Sciences Institute, University of Michigan, Ann Arbor, MI 48109, USA.
Hideyuki Komori
Cheng-Yu Lee
University of Michigan · US

Funding

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
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-GM092818NINDS NIH HHS R01 NS077914NINDS NIH HHS R01-NS077914
6 · The paper itself

Abstract

Asymmetric stem cell division balances maintenance of the stem cell pool and generation of diverse cell types by simultaneously allowing one daughter progeny to maintain a stem cell fate and its sibling to acquire a progenitor cell identity. A progenitor cell possesses restricted developmental potential, and defects in the regulation of progenitor cell potential can directly impinge on the maintenance of homeostasis and contribute to tumor initiation. Despite their importance, the molecular mechanisms underlying the precise regulation of restricted developmental potential in progenitor cells remain largely unknown. We used the type II neural stem cell (neuroblast) lineage in Drosophila larval brain as a genetic model system to investigate how an intermediate neural progenitor (INP) cell acquires restricted developmental potential. We identify the transcription factor Klumpfuss (Klu) as distinguishing a type II neuroblast from an INP in larval brains. klu functions to maintain the identity of type II neuroblasts, and klu mutant larval brains show progressive loss of type II neuroblasts due to premature differentiation. Consistently, Klu protein is detected in type II neuroblasts but is undetectable in immature INPs. Misexpression of klu triggers immature INPs to revert to type II neuroblasts. In larval brains lacking brain tumor function or exhibiting constitutively activated Notch signaling, removal of klu function prevents the reversion of immature INPs. These results led us to propose that multiple mechanisms converge to exert precise control of klu and distinguish a progenitor cell from its sibling stem cell during asymmetric neuroblast division.

Indexed as

Gene Expression RegulationNeurogenesisAnimalsAnimals, Genetically ModifiedBrainCell LineageDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsGene Expression ProfilingHomeostasisMicroscopy, FluorescenceModels, BiologicalMutationStem CellsTranscription FactorsDNA-Binding ProteinsDrosophila ProteinsKlu protein, DrosophilaTranscription Factors

Identifiers

PMID22745313
PMCPMC3392700
OpenAlexW2129422654

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.