Evidence map›Paper›PMID 27623381›Full record

ArticleDevelopmental cell2016

A Nucleoporin Docks Protein Phosphatase 1 to Direct Meiotic Chromosome Segregation and Nuclear Assembly.

Neil Hattersley, Dhanya Cheerambathur, Mark Moyle, Marine Stefanutti, Amelia Richardson, Kian-Yong Lee, Julien Dumont, Karen Oegema, Arshad Desai

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
6.4field-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

57 citing papers in PubMed, 86 citations in OpenAlex.

  1. Article
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  3. Structure, function and assembly of nuclear pore complexes.Nature reviews. Molecular cell biology · 2026
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  10. Securin Regulates the Spatiotemporal Dynamics of Separase.bioRxiv : the preprint server for biology · 2023
    Article
  11. Article
  12. Nuclear transport proteins: structure, function, and disease relevance.Signal transduction and targeted therapy · 2023
    Review
  13. Article
  14. Article
  15. Article
  16. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 3 countries.

Neil HattersleyDepartment of Cellular and Molecular Medicine, Ludwig Institute for Cancer Research, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0653, USA.
Dhanya CheerambathurDepartment of Cellular and Molecular Medicine, Ludwig Institute for Cancer Research, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0653, USA.
Mark MoyleDepartment of Cellular and Molecular Medicine, Ludwig Institute for Cancer Research, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0653, USA.
Marine StefanuttiInstitut Jacques Monod, CNRS, UMR 7592, University Paris Diderot, Sorbonne Paris Cité, 75205 Paris, France.
Amelia RichardsonDepartment of Cellular and Molecular Medicine, Ludwig Institute for Cancer Research, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0653, USA.
Kian-Yong LeeDepartment of Cellular and Molecular Medicine, Ludwig Institute for Cancer Research, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0653, USA.
Julien DumontInstitut Jacques Monod, CNRS, UMR 7592, University Paris Diderot, Sorbonne Paris Cité, 75205 Paris, France.
Karen OegemaDepartment of Cellular and Molecular Medicine, Ludwig Institute for Cancer Research, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0653, USA.
Arshad DesaiDepartment of Cellular and Molecular Medicine, Ludwig Institute for Cancer Research, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0653, USA. Electronic address: abdesai@ucsd.edu.
Ludwig Cancer Research · BECentre National de la Recherche Scientifique · FRUniversity of California San Diego · US

Funding

Kinetochore Specification and FunctionR01GM074215 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DESAI, ARSHAD · 2005 to 2025
$8.2M
NIGMS NIH HHS R01 GM074215
6 · The paper itself

Abstract

During M-phase entry in metazoans with open mitosis, the concerted action of mitotic kinases disassembles nuclei and promotes assembly of kinetochores-the primary microtubule attachment sites on chromosomes. At M-phase exit, these major changes in cellular architecture must be reversed. Here, we show that the conserved kinetochore-localized nucleoporin MEL-28/ELYS docks the catalytic subunit of protein phosphatase 1 (PP1c) to direct kinetochore disassembly-dependent chromosome segregation during oocyte meiosis I and nuclear assembly during the transition from M phase to interphase. During oocyte meiosis I, MEL-28-PP1c disassembles kinetochores in a timely manner to promote elongation of the acentrosomal spindles that segregate homologous chromosomes. During nuclear assembly, MEL-28 recruits PP1c to the periphery of decondensed chromatin, where it directs formation of a functional nuclear compartment. Thus, a pool of phosphatase activity associated with a kinetochore-localized nucleoporin contributes to two key events that occur during M-phase exit in metazoans: kinetochore disassembly and nuclear reassembly.

Indexed as

AnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsChromosome SegregationDNA-Binding ProteinsHumansKinetochoresMeiosisNuclear EnvelopeNuclear Pore Complex ProteinsNuclear ProteinsOocytesProtein Interaction MapsReceptors, Neuropeptide YCaenorhabditis elegans ProteinsDNA-Binding Proteinsmel-28 protein, C elegansneuropeptide Y4 receptorNuclear Pore Complex ProteinsNuclear ProteinsReceptors, Neuropeptide Ycentromerechromosome segregationELYSkinetochoremeiosisMEL-28nuclear porenuclear pore assemblyPP1 dockingprotein phosphatase 1

Identifiers

PMID27623381
PMCPMC5094371
OpenAlexW2519731012

What OpenQuestion holds

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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.