Evidence map›Paper›PMID 34772946›Full record

ArticleNature communications2021

Cell cycle arrest determines adult neural stem cell ontogeny by an embryonic Notch-nonoscillatory Hey1 module.

Yujin Harada, Mayumi Yamada, Itaru Imayoshi, Ryoichiro Kageyama, Yutaka Suzuki, Takaaki Kuniya, Shohei Furutachi, Daichi Kawaguchi, Yukiko Gotoh

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.4field-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

29 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Modes of Notch signalling in development and disease.Nature reviews. Molecular cell biology · 2025
    Review
  12. NOTCH Signaling Networks in Perivascular Adipose Tissue.Arteriosclerosis, thrombosis, and vascular biology · 2025
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Coupling of stemness maintenance with cell cycle control in stem cells.Frontiers in cell and developmental biology · 2025
    Review
  19. Oscillatory control of embryonic development.Development (Cambridge, England) · 2024
    Review
  20. Epigenetic regulation in adult neural stem cells.Frontiers in cell and developmental biology · 2024
    Review
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

9 authors at 3 institutions in 2 countries.

Yujin HaradaGraduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, 113-0033, Japan.
Mayumi YamadaInstitute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, 606-8507, Japan.
Itaru ImayoshiInstitute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, 606-8507, Japan.
Ryoichiro KageyamaInstitute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, 606-8507, Japan.
Yutaka SuzukiDepartment of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Chiba, 277-8562, Japan.
Takaaki KuniyaGraduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, 113-0033, Japan.
Shohei FurutachiGraduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, 113-0033, Japan.
Daichi KawaguchiGraduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, 113-0033, Japan. dkawaguchi@mol.f.u-tokyo.ac.jp.ORCID http://orcid.org/0000-0001-7387-8728
Yukiko GotohGraduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, 113-0033, Japan. ygotoh@mol.f.u-tokyo.ac.jp.ORCID http://orcid.org/0000-0001-9367-6648
The University of Tokyo · JPKyoto University · JPSainsbury Laboratory · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quiescent neural stem cells (NSCs) in the adult mouse brain are the source of neurogenesis that regulates innate and adaptive behaviors. Adult NSCs in the subventricular zone are derived from a subpopulation of embryonic neural stem-progenitor cells (NPCs) that is characterized by a slower cell cycle relative to the more abundant rapid cycling NPCs that build the brain. Yet, how slow cell cycle can cause the establishment of adult NSCs remains largely unknown. Here, we demonstrate that Notch and an effector Hey1 form a module that is upregulated by cell cycle arrest in slowly dividing NPCs. In contrast to the oscillatory expression of the Notch effectors Hes1 and Hes5 in fast cycling progenitors, Hey1 displays a non-oscillatory stationary expression pattern and contributes to the long-term maintenance of NSCs. These findings reveal a novel division of labor in Notch effectors where cell cycle rate biases effector selection and cell fate.

Indexed as

Adult Stem CellsAnimalsBasic Helix-Loop-Helix ProteinsBrainCell CycleCell Cycle CheckpointsCell Cycle ProteinsEmbryonic Stem CellsGene ExpressionLateral VentriclesMiceNervous SystemNeurogenesisReceptor, Notch1Repressor ProteinsBasic Helix-Loop-Helix ProteinsCell Cycle ProteinsHes5 protein, mouseHey1 protein, mouseNotch1 protein, mouseReceptor, Notch1Repressor Proteins

Identifiers

PMID34772946
PMCPMC8589987
OpenAlexW3213313835

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.