Evidence map›Paper›PMID 31600347›Full record

ArticlePLoS pathogens2019

Plasmodium kinesin-8X associates with mitotic spindles and is essential for oocyst development during parasite proliferation and transmission.

Mohammad Zeeshan, Fiona Shilliday, Tianyang Liu, Steven Abel, Tobias Mourier, David J P Ferguson, Edward Rea, Rebecca R Stanway, Magali Roques, Desiree Williams and 8 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 55 citations in OpenAlex.

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  18. Life science alliance · 2022
    Article
  19. Open biology · 2022
    Article
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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

18 authors at 8 institutions in 5 countries.

Mohammad ZeeshanSchool of Life Sciences, Queens Medical Centre, University of Nottingham, Nottingham, United Kingdom.ORCID 0000-0002-6185-403X
Fiona ShillidayInstitute of Structural and Molecular Biology, Department of Biological Sciences, Birkbeck College, London, United Kingdom.ORCID 0000-0002-9275-0604
Tianyang LiuInstitute of Structural and Molecular Biology, Department of Biological Sciences, Birkbeck College, London, United Kingdom.ORCID 0000-0003-2598-8572
Steven AbelDepartment of Molecular, Cell and Systems Biology, University of California Riverside, Riverside, California, United States of America.ORCID 0000-0002-4361-3443
Tobias MourierBiological Environmental Sciences and Engineering Division, King Abdullah University of Science and Technology, Thuwal, Jeddah, Kingdom of Saudi Arabia.ORCID 0000-0003-2727-1903
David J P FergusonNuffield Department of Clinical Laboratory Sciences, University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom.ORCID 0000-0001-5045-819X
Edward ReaSchool of Life Sciences, Queens Medical Centre, University of Nottingham, Nottingham, United Kingdom.ORCID 0000-0001-9826-3981
Rebecca R StanwayInstitute of Cell Biology, University of Bern, Bern, Switzerland.
Magali RoquesInstitute of Cell Biology, University of Bern, Bern, Switzerland.
Desiree WilliamsDepartment of Molecular, Cell and Systems Biology, University of California Riverside, Riverside, California, United States of America.ORCID 0000-0002-0524-2055
Emilie DanielSchool of Life Sciences, Queens Medical Centre, University of Nottingham, Nottingham, United Kingdom.ORCID 0000-0002-6570-6122
Declan BradySchool of Life Sciences, Queens Medical Centre, University of Nottingham, Nottingham, United Kingdom.ORCID 0000-0001-9150-7840
Anthony J RobertsInstitute of Structural and Molecular Biology, Department of Biological Sciences, Birkbeck College, London, United Kingdom.ORCID 0000-0001-5277-6730
Anthony A HolderMalaria Parasitology Laboratory, The Francis Crick Institute, London, United Kingdom.ORCID 0000-0002-8490-6058
Arnab PainBiological Environmental Sciences and Engineering Division, King Abdullah University of Science and Technology, Thuwal, Jeddah, Kingdom of Saudi Arabia.
Karine G Le RochDepartment of Molecular, Cell and Systems Biology, University of California Riverside, Riverside, California, United States of America.ORCID 0000-0002-4862-9292
Carolyn A MooresInstitute of Structural and Molecular Biology, Department of Biological Sciences, Birkbeck College, London, United Kingdom.ORCID 0000-0001-5686-6290
Rita TewariSchool of Life Sciences, Queens Medical Centre, University of Nottingham, Nottingham, United Kingdom.ORCID 0000-0003-3943-1847
University of Nottingham · GBInstitute of Structural and Molecular Biology · GBUniversity of California, Riverside · USUniversity of Bern · CHHokkaido University · JPKing Abdullah University of Science and Technology · SAOxford Brookes University · GBThe Francis Crick Institute · GB

Funding

Chromatin structure and control of gene expression in the human malaria parasiteR01AI136511 · NIAID · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI LE ROCH, KARINE GAELLE · 2018 to 2022
$3.4M
Biotechnology and Biological Sciences Research Council BB/N017609/1Biotechnology and Biological Sciences Research Council BB/P008348/1Cancer Research UK FC001097Medical Research Council FC001097Medical Research Council G0900109Medical Research Council G0900278Medical Research Council MR/K011782/1Medical Research Council MR/N023048/1NIAID NIH HHS R01 AI136511Wellcome Trust 104196/Z/14/ZWellcome Trust FC001097
6 · The paper itself

Abstract

Kinesin-8 proteins are microtubule motors that are often involved in regulation of mitotic spindle length and chromosome alignment. They move towards the plus ends of spindle microtubules and regulate the dynamics of these ends due, at least in some species, to their microtubule depolymerization activity. Plasmodium spp. exhibit an atypical endomitotic cell division in which chromosome condensation and spindle dynamics in the different proliferative stages are not well understood. Genome-wide shared orthology analysis of Plasmodium spp. revealed the presence of two kinesin-8 motor proteins, kinesin-8X and kinesin-8B. Here we studied the biochemical properties of kinesin-8X and its role in parasite proliferation. In vitro, kinesin-8X has motility and depolymerization activities like other kinesin-8 motors. To understand the role of Plasmodium kinesin-8X in cell division, we used fluorescence-tagging and live cell imaging to define its location, and gene targeting to analyse its function, during all proliferative stages of the rodent malaria parasite P. berghei life cycle. The results revealed a spatio-temporal involvement of kinesin-8X in spindle dynamics and an association with both mitotic and meiotic spindles and the putative microtubule organising centre (MTOC). Deletion of the kinesin-8X gene revealed a defect in oocyst development, confirmed by ultrastructural studies, suggesting that this protein is required for oocyst development and sporogony. Transcriptome analysis of Δkinesin-8X gametocytes revealed modulated expression of genes involved mainly in microtubule-based processes, chromosome organisation and the regulation of gene expression, supporting a role for kinesin-8X in cell division. Kinesin-8X is thus required for parasite proliferation within the mosquito and for transmission to the vertebrate host.

Indexed as

AnimalsChromosome SegregationFemaleKinesinsMalariaMaleMice, Inbred BALB CMicrotubulesMitosisOocystsPlasmodiumProtozoan ProteinsSpindle ApparatusKinesinsProtozoan Proteins

Identifiers

PMID31600347
PMCPMC6786531
OpenAlexW2979521730

What OpenQuestion holds

Textmetadata
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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.