Evidence map›Paper›PMID 20935513›Full record

ArticleCell cycle (Georgetown, Tex.)2010

β-Arrestin-1 links mitogenic sonic hedgehog signaling to the cell cycle exit machinery in neural precursors.

Susana R Parathath, Lori Anne Mainwaring, Africa Fernandez-L, Cemile G Guldal, Zaher Nahlé, Anna Marie Kenney

Abstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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  5. Review
  6. Article
  7. Article
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  9. Article
  10. Stem cells international · 2017
    Article
  11. Article
  12. Co-expression of β-arrestin1 and NF-кB is associated with cancer progression and poor prognosis in lung adenocarcinoma.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
  13. Tonic activation of Bax primes neural progenitors for rapid apoptosis through a mechanism preserved in medulloblastoma.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  14. Article
  15. Article
  16. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Susana R ParathathDepartment of Cancer Biology and Genetics, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
Lori Anne Mainwaring
Africa Fernandez-L
Cemile G Guldal
Zaher Nahlé
Anna Marie Kenney

Funding

Sonic hedgehog:Insulin-Like Growth Factor Interactions in Proliferating Neural PrR01NS061070 · NINDS · VANDERBILT UNIVERSITY · PI KENNEY, ANNA MARIE · 2007 to 2016
$3.5M
Sonic Hedghog Signaling in Cerebellum Development and MedulloblastomaF32AG030888 · NIA · SLOAN-KETTERING INST CAN RESEARCH · PI PARATHATH, SUSANA · 2007 to 2009
$111k
NIA NIH HHS F32 AG030888NINDS NIH HHS R01 NS061070
6 · The paper itself

Abstract

Development of the cerebellum, a brain region regulating posture and coordination, occurs post-natally and is marked by rapid proliferation of granule neuron precursors (CGNPs), stimulated by mitogenic Sonic hedgehog (Shh) signaling. β-Arrestin (βArr) proteins play important roles downstream of Smoothened, the Shh signal transducer. However, whether Shh regulates βArrs and what role they play in Shh-driven CGNP proliferation remains to be determined. Here, we report that Shh induces βArr1 accumulation and localization to the nucleus, where it participates in enhancing expression of the cyclin dependent kinase (cdk) inhibitor p27, whose accumulation eventually drives CGNP cell cycle exit. βArr1 knockdown enhances CGNP proliferation and reduces p27 expression. Thus, Shh-mediated βArr1 induction represents a novel negative feedback loop within the Shh mitogenic pathway, such that ongoing Shh signaling, while required for CGNPs to proliferate, also sets up a cell-intrinsic clock programming their ultimate exit from the cell cycle.

Indexed as

AnimalsArrestinsbeta-Arrestin 1beta-ArrestinsCell CycleCells, CulturedCerebellumCyclic AMP Response Element-Binding ProteinCyclin-Dependent Kinase Inhibitor p27Hedgehog ProteinsJNK Mitogen-Activated Protein KinasesMiceMitosisNeural Stem Cellsp300-CBP Transcription FactorsPromoter Regions, GeneticArrb1 protein, mouseArrestinsbeta-Arrestin 1beta-ArrestinsCreb1 protein, mouseCyclic AMP Response Element-Binding ProteinCyclin-Dependent Kinase Inhibitor p27Hedgehog ProteinsJNK Mitogen-Activated Protein Kinasesp300-CBP Transcription FactorsShh protein, mouse

Identifiers

PMID20935513
PMCPMC3047755

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.