Evidence map›Paper›PMID 27112495›Full record

ArticleNeuron2016

Phosphorylation of β-Tubulin by the Down Syndrome Kinase, Minibrain/DYRK1a, Regulates Microtubule Dynamics and Dendrite Morphogenesis.

Kassandra M Ori-McKenney, Richard J McKenney, Hector H Huang, Tun Li, Shan Meltzer, Lily Yeh Jan, Ronald D Vale, Arun P Wiita, Yuh Nung Jan

Open access · bronzeAbstract read
In one paragraph

Article in Neuron, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

66 citing papers in PubMed, 103 citations in OpenAlex.

  1. Review
  2. Loss ofbioRxiv : the preprint server for biology · 2026
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  7. Pharmaco-behavioral profiling identifies suppressors of autism gene-associated phenotypes in zebrafish.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  8. Article
  9. Up-regulation of Minibrain/DYRK1A contributes to macrocephaly and brain overgrowth in aProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. DYRK1A roles in human neural progenitors.Frontiers in neuroscience · 2025
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Skeletal health inFrontiers in neuroscience · 2024
    Review
  20. Article

6 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Kassandra M Ori-McKenneyDepartment of Physiology and Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, CA 94158, USA.
Richard J McKenneyDepartment of Cellular and Molecular Pharmacology and Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, CA 94158, USA.
Hector H HuangDepartment of Laboratory Medicine, University of California, San Francisco, San Francisco, CA 94158, USA.
Tun LiDepartment of Physiology and Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, CA 94158, USA.
Shan MeltzerDepartment of Physiology and Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, CA 94158, USA.
Lily Yeh JanDepartment of Physiology and Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, CA 94158, USA.
Ronald D ValeDepartment of Cellular and Molecular Pharmacology and Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, CA 94158, USA.
Arun P WiitaDepartment of Laboratory Medicine, University of California, San Francisco, San Francisco, CA 94158, USA.
Yuh Nung JanDepartment of Physiology and Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, CA 94158, USA. Electronic address: yuhnung.jan@ucsf.edu.
Howard Hughes Medical Institute · USUniversity of California, San Francisco · US

Funding

Microtubule Complexes Involved in Intracelluar TransportR37GM038499 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VALE, RONALD D · 2006 to 2015
$3.2M
GENETIC DISSECTION OF DENDRITE DEVELOPMENTR01NS040929 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JAN, YUH NUNG · 2001 to 2009
$3.1M
Genetic Dissection of Dendrite DevelopmentR37NS040929 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JAN, YUH NUNG · 2010 to 2016
$2.5M
MICROTUBULE-BASED ORGANELLE TRANSPORTR01GM038499 · NIGMS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI VALE, RONALD D · 1988 to 2005
$1.2M
Role of the Down Syndrome gene, minibrain, in neuronal development and functionR00HD080981 · NICHD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI ORI-MCKENNEY, KASSANDRA MARIE · 2016 to 2018
$708k
Role of the Down Syndrome gene, minibrain, in neuronal development and functionK99HD080981 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ORI-MCKENNEY, KASSANDRA MARIE · 2014 to 2015
$183k
Regulation of Cytoplasmic Dynein Motility in Neuronal TransportK99NS089428 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MCKENNEY, RICHARD JAMES · 2015 to 2015
$88k
Howard Hughes Medical InstituteNICHD NIH HHS K99 HD080981NICHD NIH HHS R00 HD080981NIGMS NIH HHS R01 GM038499NIGMS NIH HHS R37 GM038499NINDS NIH HHS K99 NS089428NINDS NIH HHS R01 NS040929NINDS NIH HHS R37 NS040929
6 · The paper itself

Abstract

Dendritic arborization patterns are consistent anatomical correlates of genetic disorders such as Down syndrome (DS) and autism spectrum disorders (ASDs). In a screen for abnormal dendrite development, we identified Minibrain (MNB)/DYRK1a, a kinase implicated in DS and ASDs, as a regulator of the microtubule cytoskeleton. We show that MNB is necessary to establish the length and cytoskeletal composition of terminal dendrites by controlling microtubule growth. Altering MNB levels disrupts dendrite morphology and perturbs neuronal electrophysiological activity, resulting in larval mechanosensation defects. Using in vivo and in vitro approaches, we uncover a molecular pathway whereby direct phosphorylation of β-tubulin by MNB inhibits tubulin polymerization, a function that is conserved for mammalian DYRK1a. Our results demonstrate that phosphoregulation of microtubule dynamics by MNB/DYRK1a is critical for dendritic patterning and neuronal function, revealing a previously unidentified mode of posttranslational microtubule regulation in neurons and uncovering a conserved pathway for a DS- and ASD-associated kinase.

Indexed as

AnimalsBehavior, AnimalBrainDendritesDrosophila melanogasterDrosophila ProteinsDyrk KinasesMicrotubulesNeurogenesisPhosphorylationProtein Serine-Threonine KinasesProtein-Tyrosine KinasesTubulinDrosophila ProteinsDyrk Kinasesmnb protein, DrosophilaProtein Serine-Threonine KinasesProtein-Tyrosine KinasesTubulin

Identifiers

PMID27112495
PMCPMC4860041
OpenAlexW2341496343

What OpenQuestion holds

Textmetadata
LicenceTDM
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.