Evidence map›Paper›PMID 30827898›Full record

ArticleDevelopmental cell2019

The Kinetochore-Microtubule Coupling Machinery Is Repurposed in Sensory Nervous System Morphogenesis.

Dhanya K Cheerambathur, Bram Prevo, Tiffany-Lynn Chow, Neil Hattersley, Shaohe Wang, Zhiling Zhao, Taekyung Kim, Adina Gerson-Gurwitz, Karen Oegema, Rebecca Green and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Developmental cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

32 citing papers in PubMed, 48 citations in OpenAlex.

  1. Kinetochore proteins control microtubule dynamics in postmitotic neurons to regulate the formation of dendritic spines.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. An intraflagellar transport dependent negative feedback regulates the MAPKKK DLK-1 to protect cilia from degeneration.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  14. Article
  15. Article
  16. A role for Shugoshin in human cilia?microPublication biology · 2023
    Article
  17. Article
  18. Centromere drive: model systems and experimental progress.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2022
    Review
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Dhanya K CheerambathurLudwig Institute for Cancer Research, San Diego Branch, La Jolla, CA 92093, USA; Department of Cellular & Molecular Medicine, University of California, San Diego, San Diego, La Jolla, CA 92093, USA. Electronic address: dhanya.cheerambathur@ed.ac.uk.
Bram PrevoLudwig Institute for Cancer Research, San Diego Branch, La Jolla, CA 92093, USA; Department of Cellular & Molecular Medicine, University of California, San Diego, San Diego, La Jolla, CA 92093, USA.
Tiffany-Lynn ChowLudwig Institute for Cancer Research, San Diego Branch, La Jolla, CA 92093, USA; Department of Cellular & Molecular Medicine, University of California, San Diego, San Diego, La Jolla, CA 92093, USA.
Neil HattersleyLudwig Institute for Cancer Research, San Diego Branch, La Jolla, CA 92093, USA; Department of Cellular & Molecular Medicine, University of California, San Diego, San Diego, La Jolla, CA 92093, USA.
Shaohe WangLudwig Institute for Cancer Research, San Diego Branch, La Jolla, CA 92093, USA; Department of Cellular & Molecular Medicine, University of California, San Diego, San Diego, La Jolla, CA 92093, USA.
Zhiling ZhaoLudwig Institute for Cancer Research, San Diego Branch, La Jolla, CA 92093, USA; Department of Cellular & Molecular Medicine, University of California, San Diego, San Diego, La Jolla, CA 92093, USA.
Taekyung KimLudwig Institute for Cancer Research, San Diego Branch, La Jolla, CA 92093, USA; Department of Cellular & Molecular Medicine, University of California, San Diego, San Diego, La Jolla, CA 92093, USA.
Adina Gerson-GurwitzLudwig Institute for Cancer Research, San Diego Branch, La Jolla, CA 92093, USA; Department of Cellular & Molecular Medicine, University of California, San Diego, San Diego, La Jolla, CA 92093, USA.
Karen OegemaLudwig Institute for Cancer Research, San Diego Branch, La Jolla, CA 92093, USA; Department of Cellular & Molecular Medicine, University of California, San Diego, San Diego, La Jolla, CA 92093, USA.
Rebecca GreenLudwig Institute for Cancer Research, San Diego Branch, La Jolla, CA 92093, USA; Department of Cellular & Molecular Medicine, University of California, San Diego, San Diego, La Jolla, CA 92093, USA.
Arshad DesaiLudwig Institute for Cancer Research, San Diego Branch, La Jolla, CA 92093, USA; Department of Cellular & Molecular Medicine, University of California, San Diego, San Diego, La Jolla, CA 92093, USA. Electronic address: abdesai@ucsd.edu.
University of California, San Diego · USLudwig Cancer Research · US

Funding

Kinetochore Specification and FunctionR01GM074215 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DESAI, ARSHAD · 2005 to 2025
$8.2M
NIGMS NIH HHS R01 GM074215Wellcome Trust 203149Wellcome Trust 208833Wellcome Trust 208833/Z/17/Z
6 · The paper itself

Abstract

Dynamic coupling of microtubule ends to kinetochores, built on the centromeres of chromosomes, directs chromosome segregation during cell division. Here, we report that the evolutionarily ancient kinetochore-microtubule coupling machine, the KMN (Knl1/Mis12/Ndc80-complex) network, plays a critical role in neuronal morphogenesis. We show that the KMN network concentrates in microtubule-rich dendrites of developing sensory neurons that collectively extend in a multicellular morphogenetic event that occurs during C. elegans embryogenesis. Post-mitotic degradation of KMN components in sensory neurons disrupts dendritic extension, leading to patterning and functional defects in the sensory nervous system. Structure-guided mutations revealed that the molecular interface that couples kinetochores to spindle microtubules also functions in neuronal development. These results identify a cell-division-independent function for the chromosome-segregation machinery and define a microtubule-coupling-dependent event in sensory nervous system morphogenesis.

Indexed as

MorphogenesisAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsDendritesEmbryonic DevelopmentEmbryo, NonmammalianKinetochoresMicrotubulesMitosisNervous SystemSensory Receptor CellsCaenorhabditis elegans Proteinschromosome segregationdendritekinetochoreKMN networkKnl1microtubuleMis12 complexmitosismorphogenesisNdc80 complexnervous systemsensory neuron

Identifiers

PMID30827898
PMCPMC6436928
OpenAlexW2919931991

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.