Evidence map›Paper›PMID 26114094›Full record

ArticleFrontiers in oncology2015

Spatial Separation of Plk1 Phosphorylation and Activity.

Wytse Bruinsma, Melinda Aprelia, Jolanda Kool, Libor Macurek, Arne Lindqvist, René H Medema

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

41 citing papers in PubMed, 56 citations in OpenAlex.

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  18. Moonlighting at the Poles: Non-Canonical Functions of Centrosomes.Frontiers in cell and developmental biology · 2022
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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

6 authors at 3 institutions in 3 countries.

Wytse BruinsmaDepartment of Cell Biology, The Netherlands Cancer Institute , Amsterdam , Netherlands ; Department of Medical Oncology and Cancer Genomics Center, University Medical Center Utrecht , Utrecht , Netherlands.
Melinda ApreliaDepartment of Cell Biology, The Netherlands Cancer Institute , Amsterdam , Netherlands ; Department of Medical Oncology and Cancer Genomics Center, University Medical Center Utrecht , Utrecht , Netherlands.
Jolanda KoolDepartment of Medical Oncology and Cancer Genomics Center, University Medical Center Utrecht , Utrecht , Netherlands.
Libor MacurekDepartment of Medical Oncology and Cancer Genomics Center, University Medical Center Utrecht , Utrecht , Netherlands ; Laboratory of Cancer Cell Biology, Institute of Molecular Genetics of the ASCR, v. v. i. , Prague , Czech Republic.
Arne LindqvistDepartment of Medical Oncology and Cancer Genomics Center, University Medical Center Utrecht , Utrecht , Netherlands ; Department of Cell and Molecular Biology, Karolinska Institute , Stockholm , Sweden.
René H MedemaDepartment of Cell Biology, The Netherlands Cancer Institute , Amsterdam , Netherlands ; Department of Medical Oncology and Cancer Genomics Center, University Medical Center Utrecht , Utrecht , Netherlands.
Cancer Genomics Centre · NLThe Netherlands Cancer Institute · NLUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polo-like kinase 1 (Plk1) is one of the major kinases controlling mitosis and cell division. Plk1 is first recruited to the centrosome in S phase, then appears on the kinetochores in late G2, and at the end of mitosis, it translocates to the central spindle. Activation of Plk1 requires phosphorylation of T210 by Aurora A, an event that critically depends on the co-factor Bora. However, conflicting reports exist as to where Plk1 is first activated. Phosphorylation of T210 is first observed at the centrosomes, but kinase activity seems to be restricted to the nucleus in the earlier phases of G2. Here, we demonstrate that Plk1 activity manifests itself first in the nucleus using a nuclear FRET-based biosensor for Plk1 activity. However, we find that Bora is restricted to the cytoplasm and that Plk1 is phosphorylated on T210 at the centrosomes. Our data demonstrate that while Plk1 activation occurs on centrosomes, downstream target phosphorylation by Plk1 first occurs in the nucleus. We discuss several explanations for this surprising separation of activation and function.

Indexed as

aurora kinaseboracell cyclecheckpoint recoveryplk1

Identifiers

PMID26114094
PMCPMC4462105
OpenAlexW1554725406

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.