Evidence map›Paper›PMID 26487778›Full record

ArticleDevelopment (Cambridge, England)2015

Lin-28 promotes symmetric stem cell division and drives adaptive growth in the adult Drosophila intestine.

Ching-Huan Chen, Arthur Luhur, Nicholas Sokol

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

31 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Gene model for the ortholog ofmicroPublication biology · 2025
    Article
  5. Gene model for the ortholog ofmicroPublication biology · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. Tissue Homeostasis and Non-Homeostasis: From Cell Life Cycles to Organ States.Annual review of cell and developmental biology · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Emerging Roles of RNA-Binding Proteins in Neurodevelopment.Journal of developmental biology · 2022
    Review
  14. Article
  15. A stress-responsive miRNA regulates BMP signaling to maintain tissue homeostasis.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  16. Article
  17. I-KCKT allows dissection-free RNA profiling of adultDevelopment (Cambridge, England) · 2021
    Article
  18. Review
  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.

Ching-Huan ChenDepartment of Biology, Indiana University, Bloomington, IN 47405, USA.
Arthur LuhurDepartment of Biology, Indiana University, Bloomington, IN 47405, USA.
Nicholas SokolDepartment of Biology, Indiana University, Bloomington, IN 47405, USA nsokol@indiana.edu.
Indiana University Bloomington · US

Funding

The Control of Neuronal Diversity and Plasticity by the let-7-C microRNA PathwayR01MH087511 · NIMH · TRUSTEES OF INDIANA UNIVERSITY · PI SOKOL, NICHOLAS · 2009 to 2013
$1.7M
Lin-28 and the translational control of stem cell metabolismR21OD019916 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI SOKOL, NICHOLAS · 2015 to 2016
$409k
NIH HHS R21 OD019916NIH HHS R21OD019916NIMH NIH HHS R01 MH087511NIMH NIH HHS R01MH087511
6 · The paper itself

Abstract

Stem cells switch between asymmetric and symmetric division to expand in number as tissues grow during development and in response to environmental changes. The stem cell intrinsic proteins controlling this switch are largely unknown, but one candidate is the Lin-28 pluripotency factor. A conserved RNA-binding protein that is downregulated in most animals as they develop from embryos to adults, Lin-28 persists in populations of adult stem cells. Its function in these cells has not been previously characterized. Here, we report that Lin-28 is highly enriched in adult intestinal stem cells in the Drosophila intestine. lin-28 null mutants are homozygous viable but display defects in this population of cells, which fail to undergo a characteristic food-triggered expansion in number and have reduced rates of symmetric division as well as reduced insulin signaling. Immunoprecipitation of Lin-28-bound mRNAs identified Insulin-like Receptor (InR), forced expression of which completely rescues lin-28-associated defects in intestinal stem cell number and division pattern. Furthermore, this stem cell activity of lin-28 is independent of one well-known lin-28 target, the microRNA let-7, which has limited expression in the intestinal epithelium. These results identify Lin-28 as a stem cell intrinsic factor that boosts insulin signaling in intestinal progenitor cells and promotes their symmetric division in response to nutrients, defining a mechanism through which Lin-28 controls the adult stem cell division patterns that underlie tissue homeostasis and regeneration.

Indexed as

AnimalsCell DivisionDrosophila melanogasterDrosophila ProteinsFemaleGenotypeGreen Fluorescent ProteinsHomozygoteInsulinIntestinal MucosaMicroRNAsMutationReceptor Protein-Tyrosine KinasesRegenerationRNA-Binding ProteinsRNA, MessengerDrosophila ProteinsGreen Fluorescent ProteinsInR protein, DrosophilaInsulinLet-7 microRNA, DrosophilaLin-28 protein, DrosophilaMicroRNAsReceptor Protein-Tyrosine KinasesRNA-Binding ProteinsRNA, MessengerDrosophilaIntestinal stem cellLin-28Symmetric renewal

Identifiers

PMID26487778
PMCPMC4631770
OpenAlexW1795553829

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.