Evidence map›Paper›PMID 29335529›Full record

ArticleNature cell biology2018

Transient Scute activation via a self-stimulatory loop directs enteroendocrine cell pair specification from self-renewing intestinal stem cells.

Jun Chen, Na Xu, Chenhui Wang, Pin Huang, Huanwei Huang, Zhen Jin, Zhongsheng Yu, Tao Cai, Renjie Jiao, Rongwen Xi

Erratum issuedAbstract read
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In one paragraph

Article in Nature cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing 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

60 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Jun ChenGraduate School of Peking Union Medical College, Beijing, China.
Na XuNational Institute of Biological Sciences, Beijing, China.
Chenhui WangNational Institute of Biological Sciences, Beijing, China.
Pin HuangNational Institute of Biological Sciences, Beijing, China.
Huanwei HuangNational Institute of Biological Sciences, Beijing, China.
Zhen JinNational Institute of Biological Sciences, Beijing, China.
Zhongsheng YuInstitute of Biophysics, Chinese Academy of Sciences, Beijing, China.
Tao CaiNational Institute of Biological Sciences, Beijing, China.
Renjie JiaoInstitute of Biophysics, Chinese Academy of Sciences, Beijing, China.
Rongwen XiGraduate School of Peking Union Medical College, Beijing, China. xirongwen@nibs.ac.cn.ORCID 0000-0001-5543-1236

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The process through which multiple types of cell-lineage-restricted progenitor cells are specified from multipotent stem cells is unclear. Here we show that, in intestinal stem cell lineages in adult Drosophila, in which the Delta-Notch-signalling-guided progenitor cell differentiation into enterocytes is the default mode, the specification of enteroendocrine cells (EEs) is initiated by transient Scute activation in a process driven by transcriptional self-stimulation combined with a negative feedback regulation between Scute and Notch targets. Scute activation induces asymmetric intestinal stem cell divisions that generate EE progenitor cells. The mitosis-inducing and fate-inducing activities of Scute guide each EE progenitor cell to divide exactly once prior to its terminal differentiation, yielding a pair of EEs. The transient expression of a fate inducer therefore specifies both type and numbers of committed progenitor cells originating from stem cells, which could represent a general mechanism used for diversifying committed progenitor cells from multipotent stem cells.

Indexed as

AnimalsCell DifferentiationCell LineageCell Self RenewalDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsEnteroendocrine CellsIntestinesIntracellular Signaling Peptides and ProteinsMembrane ProteinsReceptors, NotchSignal TransductionStem CellsTranscription Factorsdelta proteinDNA-Binding ProteinsDrosophila ProteinsIntracellular Signaling Peptides and ProteinsMembrane ProteinsN protein, DrosophilaReceptors, Notchsc protein, DrosophilaTranscription Factors

Identifiers

What OpenQuestion holds

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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.