Evidence map›Paper›PMID 27697906›Full record

ArticleDevelopment (Cambridge, England)2016

Nuclei migrate through constricted spaces using microtubule motors and actin networks in C. elegans hypodermal cells.

Courtney R Bone, Yu-Tai Chang, Natalie E Cain, Shaun P Murphy, Daniel A Starr

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

34 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. A gene expression atlas of a juvenile nervous system.bioRxiv : the preprint server for biology · 2025
    Article
  5. Article
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  14. Article
  15. [Advances in cell nuclear mechanobiology and its regulation mechanisms].Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi · 2023
    Review
  16. Article
  17. Article
  18. Article
  19. Split-GFP lamin as a tool for studyingmicroPublication biology · 2023
    Article
  20. Article
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

5 authors at 1 institution in 1 country.

Courtney R BoneDepartment of Molecular and Cellular Biology, University of California, Davis, CA 95616, USA.
Yu-Tai ChangDepartment of Molecular and Cellular Biology, University of California, Davis, CA 95616, USA.
Natalie E CainDepartment of Molecular and Cellular Biology, University of California, Davis, CA 95616, USA.
Shaun P MurphyDepartment of Molecular and Cellular Biology, University of California, Davis, CA 95616, USA.
Daniel A StarrDepartment of Molecular and Cellular Biology, University of California, Davis, CA 95616, USA dastarr@ucdavis.edu.ORCID 0000-0001-7339-6606
University of California, Davis · US

Funding

UC Davis MCB T32 Administrative Supplement to Recognize Excellence in Diversity, Equity, Inclusion, and Accessibility (DEIA) MentorshipT32GM007377 · NIGMS · UNIVERSITY OF CALIFORNIA DAVIS · PI CHEDIN, FREDERIC LOUIS · 1985 to 2023
$9.9M
Mechanisms of Nuclear Migration and AnchorageR01GM073874 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI STARR, DANIEL A · 2006 to 2019
$4.5M
Analysis of novel pathways for nuclear migration.F32GM106730 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI MURPHY, SHAUN P. · 2013 to 2014
$67k
NIGMS NIH HHS F32 GM106730NIGMS NIH HHS R01 GM073874NIGMS NIH HHS T32 GM007377
6 · The paper itself

Abstract

Cellular migrations through constricted spaces are a crucial aspect of many developmental and disease processes including hematopoiesis, inflammation and metastasis. A limiting factor in these events is nuclear deformation. Here, we establish an in vivo model in which nuclei can be visualized while moving through constrictions and use it to elucidate mechanisms for nuclear migration. C. elegans hypodermal P-cell larval nuclei traverse a narrow space that is about 5% their width. This constriction is blocked by fibrous organelles, structures that pass through P cells to connect the muscles to cuticle. Fibrous organelles are removed just prior to nuclear migration, when nuclei and lamins undergo extreme morphological changes to squeeze through the space. Both actin and microtubule networks are organized to mediate nuclear migration. The LINC complex, consisting of the SUN protein UNC-84 and the KASH protein UNC-83, recruits dynein and kinesin-1 to the nuclear surface. Both motors function in P-cell nuclear migration, but dynein, functioning through UNC-83, plays a more central role as nuclei migrate towards minus ends of polarized microtubule networks. Thus, the nucleoskeleton and cytoskeleton are coordinated to move nuclei through constricted spaces.

Indexed as

Caenorhabditis elegansActin CytoskeletonActinsAnimalsAnimals, Genetically ModifiedBiological TransportBody PatterningCaenorhabditis elegans ProteinsCell NucleusCytoskeletonDermisEmbryo, NonmammalianMicrotubulesActinsCaenorhabditis elegans ProteinsC. elegansDyneinKASHNuclear migrationSUN

Identifiers

PMID27697906
PMCPMC5117218
OpenAlexW2529021344

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.