Evidence map›Paper›PMID 29311228›Full record

ArticleThe Journal of cell biology2018

TPXL-1 activates Aurora A to clear contractile ring components from the polar cortex during cytokinesis.

Sriyash Mangal, Jennifer Sacher, Taekyung Kim, Daniel Sampaio Osório, Fumio Motegi, Ana Xavier Carvalho, Karen Oegema, Esther Zanin

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

42 citing papers in PubMed, 66 citations in OpenAlex.

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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

8 authors at 4 institutions in 4 countries.

Sriyash MangalCenter for Integrated Protein Science, Department Biology II, Ludwig-Maximilians University Munich, Planegg-Martinsried, Germany.
Jennifer SacherCenter for Integrated Protein Science, Department Biology II, Ludwig-Maximilians University Munich, Planegg-Martinsried, Germany.
Taekyung KimDepartment of Cellular and Molecular Medicine, Ludwig Institute for Cancer Research, University of California, San Diego, La Jolla, CA.
Daniel Sampaio OsórioInstituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.ORCID 0000-0003-4144-8189
Fumio MotegiResearch Link, National University of Singapore, Singapore.ORCID 0000-0001-9058-6559
Ana Xavier CarvalhoInstituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.ORCID 0000-0002-2256-7134
Karen OegemaDepartment of Cellular and Molecular Medicine, Ludwig Institute for Cancer Research, University of California, San Diego, La Jolla, CA koegema@ucsd.edu.ORCID 0000-0001-8515-7514
Esther ZaninCenter for Integrated Protein Science, Department Biology II, Ludwig-Maximilians University Munich, Planegg-Martinsried, Germany zanin@bio.lmu.de.ORCID 0000-0003-1450-8684
Center for Integrated Protein Science Munich · DEi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto · PTUniversity of California San Diego · USNational University of Singapore · SG

Funding

Kinetochore Specification and FunctionR01GM074215 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DESAI, ARSHAD · 2005 to 2025
$8.2M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Analysis of Centrosome DynamicsR01GM074207 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI OEGEMA, KAREN F · 2006 to 2025
$6.6M
NIGMS NIH HHS R01 GM074207NIGMS NIH HHS R01 GM074215NIH HHS P40 OD010440
6 · The paper itself

Abstract

During cytokinesis, a signal from the central spindle that forms between the separating anaphase chromosomes promotes the accumulation of contractile ring components at the cell equator, while a signal from the centrosomal microtubule asters inhibits accumulation of contractile ring components at the cell poles. However, the molecular identity of the inhibitory signal has remained unknown. To identify molecular components of the aster-based inhibitory signal, we developed a means to monitor the removal of contractile ring proteins from the polar cortex after anaphase onset. Using this assay, we show that polar clearing is an active process that requires activation of Aurora A kinase by TPXL-1. TPXL-1 concentrates on astral microtubules coincident with polar clearing in anaphase, and its ability to recruit Aurora A and activate its kinase activity are essential for clearing. In summary, our data identify Aurora A kinase as an aster-based inhibitory signal that restricts contractile ring components to the cell equator during cytokinesis.

Indexed as

AnaphaseAnimalsAurora Kinase ACaenorhabditis elegansCaenorhabditis elegans ProteinsCarrier ProteinsCytokinesisEnzyme ActivationMicrotubulesSignal TransductionAurora Kinase ACaenorhabditis elegans ProteinsCarrier ProteinsTPXL-1 protein, C elegans

Identifiers

PMID29311228
PMCPMC5839786
OpenAlexW2763852829

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.