Evidence map›Paper›PMID 26322925›Full record

ArticleNature neuroscience2015

Centrosomin represses dendrite branching by orienting microtubule nucleation.

Cagri Yalgin, Saman Ebrahimi, Caroline Delandre, Li Foong Yoong, Saori Akimoto, Heidi Tran, Reiko Amikura, Rebecca Spokony, Benjamin Torben-Nielsen, Kevin P White and 1 more

Abstract read
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In one paragraph

Article in Nature neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing 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

69 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. The Neuronal Golgi Network and Its Acolytes.Sub-cellular biochemistry · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Live Imaging of Golgi Outposts in Drosophila Dendritic Arbors.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  19. Article
  20. Article

9 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

11 authors.

Cagri YalginLaboratory for Genetic Control of Neuronal Architecture, RIKEN Brain Science Institute, Wako-shi, Saitama, Japan.
Saman EbrahimiLaboratory for Genetic Control of Neuronal Architecture, RIKEN Brain Science Institute, Wako-shi, Saitama, Japan.
Caroline DelandreLaboratory for Genetic Control of Neuronal Architecture, RIKEN Brain Science Institute, Wako-shi, Saitama, Japan.
Li Foong YoongLaboratory for Genetic Control of Neuronal Architecture, RIKEN Brain Science Institute, Wako-shi, Saitama, Japan.
Saori AkimotoLaboratory for Genetic Control of Neuronal Architecture, RIKEN Brain Science Institute, Wako-shi, Saitama, Japan.
Heidi TranLaboratory for Genetic Control of Neuronal Architecture, RIKEN Brain Science Institute, Wako-shi, Saitama, Japan.
Reiko AmikuraLaboratory for Genetic Control of Neuronal Architecture, RIKEN Brain Science Institute, Wako-shi, Saitama, Japan.
Rebecca SpokonyInstitute for Genomics and Systems Biology, Department of Human Genetics, The University of Chicago, Chicago, Illinois, USA.
Benjamin Torben-NielsenComputational Neuroscience Unit, Okinawa Institute of Science and Technology Graduate University, Onna-son, Kunigami, Okinawa, Japan.
Kevin P WhiteInstitute for Genomics and Systems Biology, Department of Human Genetics, The University of Chicago, Chicago, Illinois, USA.
Adrian W MooreLaboratory for Genetic Control of Neuronal Architecture, RIKEN Brain Science Institute, Wako-shi, Saitama, Japan.ORCID http://orcid.org/0000-0002-8242-301X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuronal dendrite branching is fundamental for building nervous systems. Branch formation is genetically encoded by transcriptional programs to create dendrite arbor morphological diversity for complex neuronal functions. In Drosophila sensory neurons, the transcription factor Abrupt represses branching via an unknown effector pathway. Targeted screening for branching-control effectors identified Centrosomin, the primary centrosome-associated protein for mitotic spindle maturation. Centrosomin repressed dendrite branch formation and was used by Abrupt to simplify arbor branching. Live imaging revealed that Centrosomin localized to the Golgi cis face and that it recruited microtubule nucleation to Golgi outposts for net retrograde microtubule polymerization away from nascent dendrite branches. Removal of Centrosomin enabled the engagement of wee Augmin activity to promote anterograde microtubule growth into the nascent branches, leading to increased branching. The findings reveal that polarized targeting of Centrosomin to Golgi outposts during elaboration of the dendrite arbor creates a local system for guiding microtubule polymerization.

Indexed as

AnimalsAnimals, Genetically ModifiedCell PolarityChromatin ImmunoprecipitationDendritesDrosophila melanogasterDrosophila ProteinsHomeodomain ProteinsMicrotubulesNeurogenesisPolymerase Chain ReactionSensory Receptor Cellscnn protein, DrosophilaDrosophila ProteinsHomeodomain Proteins

Identifiers

PMID26322925

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.