Evidence map›Paper›PMID 26953351›Full record

ArticleThe Journal of cell biology2016

Arl2- and Msps-dependent microtubule growth governs asymmetric division.

Keng Chen, Chwee Tat Koe, Zhanyuan Benny Xing, Xiaolin Tian, Fabrizio Rossi, Cheng Wang, Quan Tang, Wenhui Zong, Wan Jin Hong, Reshma Taneja and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2016. 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
2.1field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  4. A fly's eye view of quiescent neural stem cells.Oxford open neuroscience · 2022
    Review
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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

15 authors at 6 institutions in 3 countries.

Keng ChenNeuroscience and Behavioral Disorders Program, Duke-National University of Singapore Graduate Medical School, Singapore 169857 National University of Singapore Graduate School for Integrative Sciences and Engineering, National University of Singapore, Singapore 117456.
Chwee Tat KoeNeuroscience and Behavioral Disorders Program, Duke-National University of Singapore Graduate Medical School, Singapore 169857 National University of Singapore Graduate School for Integrative Sciences and Engineering, National University of Singapore, Singapore 117456.
Zhanyuan Benny XingDepartment of Cell Biology, Duke University, Duke University Medical Center, Durham, NC 27710.
Xiaolin TianNeuroscience Center of Excellence, Department of Cell Biology and Anatomy, Louisiana State University Health Sciences Center, New Orleans, LA 70112.
Fabrizio RossiInstitute for Research in Biomedicine Barcelona, 08028 Barcelona, Spain.
Cheng WangNeuroscience and Behavioral Disorders Program, Duke-National University of Singapore Graduate Medical School, Singapore 169857.
Quan TangTemasek Life Sciences Laboratory, National University of Singapore, Singapore 117604 Department of Biological Sciences, National University of Singapore, Singapore 117604.
Wenhui ZongTemasek Life Sciences Laboratory, National University of Singapore, Singapore 117604 Department of Biological Sciences, National University of Singapore, Singapore 117604.
Wan Jin HongInstitute of Molecular and Cell Biology, Singapore 138673.
Reshma TanejaNational University of Singapore Graduate School for Integrative Sciences and Engineering, National University of Singapore, Singapore 117456 Department of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117597.
Fengwei YuNeuroscience and Behavioral Disorders Program, Duke-National University of Singapore Graduate Medical School, Singapore 169857 National University of Singapore Graduate School for Integrative Sciences and Engineering, National University of Singapore, Singapore 117456 Temasek Life Sciences Laboratory, National University of Singapore, Singapore 117604 Department of Biological Sciences, National University of Singapore, Singapore 117604.
Cayetano GonzalezInstitute for Research in Biomedicine Barcelona, 08028 Barcelona, Spain Institució Catalana de Recerca i Estudis Avançats, 08010 Barcelona, Spain.
Chunlai WuNeuroscience Center of Excellence, Department of Cell Biology and Anatomy, Louisiana State University Health Sciences Center, New Orleans, LA 70112.
Sharyn EndowNeuroscience and Behavioral Disorders Program, Duke-National University of Singapore Graduate Medical School, Singapore 169857 Department of Cell Biology, Duke University, Duke University Medical Center, Durham, NC 27710.
Hongyan WangNeuroscience and Behavioral Disorders Program, Duke-National University of Singapore Graduate Medical School, Singapore 169857 National University of Singapore Graduate School for Integrative Sciences and Engineering, National University of Singapore, Singapore 117456 Department of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117597 hongyan.wang@duke-nus.edu.sg.
National University of Singapore · SGInstitute for Research in Biomedicine · ESLouisiana State University Health Sciences Center New Orleans · USDuke University · USDuke University Hospital · USInstitute of Molecular and Cell Biology · SG

Funding

Wrd-specific PP2A substrates that regulate AZ stabilityR21NS091892 · NINDS · LSU HEALTH SCIENCES CENTER · PI WU, CHUNLAI · 2015 to 2016
$402k
NINDS NIH HHS R21 NS091892
6 · The paper itself

Abstract

Asymmetric division of neural stem cells is a fundamental strategy to balance their self-renewal and differentiation. It is long thought that microtubules are not essential for cell polarity in asymmetrically dividing Drosophila melanogaster neuroblasts (NBs; neural stem cells). Here, we show that Drosophila ADP ribosylation factor like-2 (Arl2) and Msps, a known microtubule-binding protein, control cell polarity and spindle orientation of NBs. Upon arl2 RNA intereference, Arl2-GDP expression, or arl2 deletions, microtubule abnormalities and asymmetric division defects were observed. Conversely, overactivation of Arl2 leads to microtubule overgrowth and depletion of NBs. Arl2 regulates microtubule growth and asymmetric division through localizing Msps to the centrosomes in NBs. Moreover, Arl2 regulates dynein function and in turn centrosomal localization of D-TACC and Msps. Arl2 physically associates with tubulin cofactors C, D, and E. Arl2 functions together with tubulin-binding cofactor D to control microtubule growth, Msps localization, and NB self-renewal. Therefore, Arl2- and Msps-dependent microtubule growth is a new paradigm regulating asymmetric division of neural stem cells.

Indexed as

ADP-Ribosylation FactorsAnimalsCell DivisionCell PolarityCells, CulturedCentrosomeDrosophila melanogasterDrosophila ProteinsMembrane ProteinsMicrotubule-Associated ProteinsMicrotubulesNeural Stem CellsProtein BindingTubulinADP-ribosylation factor related proteinsADP-Ribosylation FactorsDrosophila ProteinsMembrane ProteinsMicrotubule-Associated Proteinsmsps protein, DrosophilaTubulin

Identifiers

PMID26953351
PMCPMC4792071
OpenAlexW2300209944

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.