Evidence map›Paper›PMID 27585866›Full record

ArticleThe EMBO journal2016

PRC2 preserves intestinal progenitors and restricts secretory lineage commitment.

Fulvio Chiacchiera, Alessandra Rossi, SriGanesh Jammula, Marika Zanotti, Diego Pasini

Abstract read
In one paragraph

Article in The EMBO journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
–field-weighted citation impact
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

59 citing papers in PubMed.

  1. Article
  2. HAT1 Regulates Intestinal Stem Cell Proliferation and Differentiation.bioRxiv : the preprint server for biology · 2026
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  5. Review
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  12. Article
  13. ECM and epithelial stem cells: the scaffold of destiny.Frontiers in cell and developmental biology · 2024
    Review
  14. Article
  15. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Fulvio ChiacchieraDepartment of Experimental Oncology, European Institute of Oncology, Milan, Italy fulvio.chiacchiera@ieo.eu diego.pasini@ieo.eu.
Alessandra RossiDepartment of Experimental Oncology, European Institute of Oncology, Milan, Italy.
SriGanesh JammulaDepartment of Experimental Oncology, European Institute of Oncology, Milan, Italy.
Marika ZanottiDepartment of Experimental Oncology, European Institute of Oncology, Milan, Italy.
Diego PasiniDepartment of Experimental Oncology, European Institute of Oncology, Milan, Italy fulvio.chiacchiera@ieo.eu diego.pasini@ieo.eu.ORCID 0000-0002-9879-6486

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chromatin modifications shape cell heterogeneity by activating and repressing defined sets of genes involved in cell proliferation, differentiation and development. Polycomb-repressive complexes (PRCs) act synergistically during development and differentiation by maintaining transcriptional repression of common genes. PRC2 exerts this activity by catalysing H3K27 trimethylation. Here, we show that in the intestinal epithelium PRC2 is required to sustain progenitor cell proliferation and the correct balance between secretory and absorptive lineage differentiation programs. Using genetic models, we show that PRC2 activity is largely dispensable for intestinal stem cell maintenance but is strictly required for radiation-induced regeneration by preventing Cdkn2a transcription. Combining these models with genomewide molecular analysis, we further demonstrate that preferential accumulation of secretory cells does not result from impaired proliferation of progenitor cells induced by Cdkn2a activation but rather from direct regulation of transcription factors responsible for secretory lineage commitment. Overall, our data uncover a dual role of PRC2 in intestinal homeostasis highlighting the importance of this repressive layer in controlling cell plasticity and lineage choices in adult tissues.

Indexed as

AnimalsCell DifferentiationCell ProliferationEmbryonic Stem CellsHistonesIntestinal MucosaMice, TransgenicPolycomb Repressive Complex 2HistonesPolycomb Repressive Complex 2chromatin modificationsH3K27 methylationintestinal homeostasis and differentiationpolycombPRC2

Identifiers

PMID27585866
PMCPMC5090213

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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.