Evidence map›Paper›PMID 23122292›Full record

ArticleCell stem cell2012

A self-limiting switch based on translational control regulates the transition from proliferation to differentiation in an adult stem cell lineage.

Megan L Insco, Alexis S Bailey, Jongmin Kim, Gonzalo H Olivares, Orly L Wapinski, Cheuk Ho Tam, Margaret T Fuller

Open access · bronzeAbstract read
In one paragraph

Article in Cell stem cell, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

53 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
  2. miR-10-3p, but not miR-1006-3p, regulatesmicroPublication biology · 2026
    Article
  3. Article
  4. Article
  5. An RNA-binding regulatory cascade controls the switch from proliferation to differentiation in theProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Article
  7. Article
  8. YTHDC2 serves a distinct late role in spermatocytes during germ cell differentiation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  9. Article
  10. Deficiency ofInternational journal of molecular sciences · 2024
    Article
  11. Article
  12. Article
  13. microPublication biology · 2023
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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.

Megan L InscoDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305-5329, USA.
Alexis S Bailey
Jongmin Kim
Gonzalo H Olivares
Orly L Wapinski
Cheuk Ho Tam
Margaret T Fuller
Stanford University · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007365 · NIGMS · STANFORD UNIVERSITY · PI CHUA, KATRIN F · 1985 to 2021
$33.8M
Leveraging innovative technologies in basic and clinical cancer researchT32CA009302 · NCI · STANFORD UNIVERSITY · PI LAURA D ATTARDI, Aaron M Newman · 1985 to 2026
$19.1M
Regulation of Stem Cell Self-Renewal and DifferentiationR01GM080501 · NIGMS · STANFORD UNIVERSITY · PI FULLER, MARGARET T · 2007 to 2019
$3.8M
NCI NIH HHS 5T32 CA009302-33NCI NIH HHS T32 CA009302NIGMS NIH HHS GM007365NIGMS NIH HHS R01 GM080501NIGMS NIH HHS T32 GM007365
6 · The paper itself

Abstract

In adult stem cell lineages, progenitor cells commonly undergo mitotic transit amplifying (TA) divisions before terminal differentiation, allowing production of many differentiated progeny per stem cell division. Mechanisms that limit TA divisions and trigger the switch to differentiation may protect against cancer by preventing accumulation of oncogenic mutations in the proliferating population. Here we show that the switch from TA proliferation to differentiation in the Drosophila male germline stem cell lineage is mediated by translational control. The TRIM-NHL tumor suppressor homolog Mei-P26 facilitates accumulation of the differentiation regulator Bam in TA cells. In turn, Bam and its partner Bgcn bind the mei-P26 3' untranslated region and repress translation of mei-P26 in late TA cells. Thus, germ cells progress through distinct, sequential regulatory states, from Mei-P26 on/Bam off to Bam on/Mei-P26 off. TRIM-NHL homologs across species facilitate the switch from proliferation to differentiation, suggesting a conserved developmentally programmed tumor suppressor mechanism.

Indexed as

Cell DifferentiationCell LineageGene Expression RegulationAdult Stem CellsAnimalsCell DivisionDNA HelicasesDrosophilaDrosophila ProteinsGerm CellsMalebam protein, Drosophilabgcn protein, DrosophilaDNA HelicasesDrosophila ProteinsMei-P26 protein, Drosophila

Identifiers

PMID23122292
PMCPMC3833810
OpenAlexW2009605610

What OpenQuestion holds

Textmetadata
LicenceTDM
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.