Evidence map›Paper›PMID 39433738›Full record

ArticleNature communications2024

Kinetochore dynein is sufficient to biorient chromosomes and remodel the outer kinetochore.

Bram Prevo, Dhanya K Cheerambathur, William C Earnshaw, Arshad Desai

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Structure and function of the outer kinetochore.Nature reviews. Molecular cell biology · 2026
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Bram PrevoWellcome Centre for Cell Biology, University of Edinburgh, Edinburgh, UK. bram.prevo@ed.ac.uk.ORCID 0000-0002-6526-5590
Dhanya K CheerambathurWellcome Centre for Cell Biology, University of Edinburgh, Edinburgh, UK.
William C EarnshawWellcome Centre for Cell Biology, University of Edinburgh, Edinburgh, UK.ORCID 0000-0002-7191-0621
Arshad DesaiLudwig Institute for Cancer Research, La Jolla, CA, USA. abdesai@ucsd.edu.ORCID 0000-0002-5410-1830

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 107022Wellcome Trust 208833Wellcome Trust 208833/Z/17/ZWellcome Trust 215925
6 · The paper itself

Abstract

Multiple microtubule-directed activities concentrate on mitotic chromosomes to ensure their faithful segregation. These include couplers and dynamics regulators localized at the kinetochore, the microtubule interface built on centromeric chromatin, as well as motor proteins recruited to kinetochores and chromatin. Here, we describe an in vivo approach in the C. elegans one-cell embryo in which removal of the major microtubule-directed activities on mitotic chromosomes is compared to the selective presence of individual activities. Our approach reveals that the kinetochore dynein module, comprised of cytoplasmic dynein and its kinetochore-specific adapters, is sufficient to biorient chromosomes; by contrast, this module is unable to support congression. In coordination with orientation, the dynein module directs removal of outermost kinetochore components, including dynein itself, independently of the other microtubule-directed activities and kinetochore-localized protein phosphatase 1. These observations indicate that the kinetochore dynein module is sufficient to biorient chromosomes and to direct remodeling of the outer kinetochore in a microtubule attachment state-sensitive manner.

Indexed as

Caenorhabditis elegansCaenorhabditis elegans ProteinsChromosome SegregationDyneinsKinetochoresMicrotubulesAnimalsChromosomesMitosisProtein Phosphatase 1Caenorhabditis elegans ProteinsDyneinsProtein Phosphatase 1

Identifiers

PMID39433738
PMCPMC11494143

What Socratic 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 Socratic graph.