Evidence map›Paper›PMID 35900985›Full record

ArticlePLoS biology2022

Genome-wide functional analysis reveals key roles for kinesins in the mammalian and mosquito stages of the malaria parasite life cycle.

Mohammad Zeeshan, Ravish Rashpa, David J P Ferguson, Steven Abel, Zeinab Chahine, Declan Brady, Sue Vaughan, Carolyn A Moores, Karine G Le Roch, Mathieu Brochet and 2 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

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  11. Microbiology spectrum · 2022
    Article
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

12 authors at 6 institutions in 3 countries.

Mohammad ZeeshanUniversity of Nottingham, School of Life Sciences, Nottingham, United Kingdom.
Ravish RashpaUniversity of Geneva, Faculty of Medicine, Geneva, Switzerland.
David J P FergusonOxford Brookes University, Department of Biological and Medical Sciences, Oxford, United Kingdom.
Steven AbelDepartment of Molecular, Cell and Systems Biology, University of California Riverside, Riverside, California, United States of America.
Zeinab ChahineDepartment of Molecular, Cell and Systems Biology, University of California Riverside, Riverside, California, United States of America.
Declan BradyUniversity of Nottingham, School of Life Sciences, Nottingham, United Kingdom.
Sue VaughanOxford Brookes University, Department of Biological and Medical Sciences, Oxford, United Kingdom.
Carolyn A MooresInstitute of Structural and Molecular Biology, Department of Biological Sciences, Birkbeck College, London, United Kingdom.
Karine G Le RochDepartment of Molecular, Cell and Systems Biology, University of California Riverside, Riverside, California, United States of America.
Mathieu BrochetUniversity of Geneva, Faculty of Medicine, Geneva, Switzerland.
Anthony A HolderThe Francis Crick Institute, Malaria Parasitology Laboratory, London, United Kingdom.
Rita TewariUniversity of Nottingham, School of Life Sciences, Nottingham, United Kingdom.ORCID 0000-0003-3943-1847
University of California, Riverside · USUniversity of Nottingham · GBOxford Brookes University · GBUniversity of Geneva · CHInstitute of Structural and Molecular Biology · 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
Evolution of the 3D chromatin structure in apicomplexan parasitesR21AI142506 · NIAID · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI LE ROCH, KARINE GAELLE · 2019 to 2020
$479k
Biotechnology and Biological Sciences Research Council BB/N017609/1Biotechnology and Biological Sciences Research Council BB/N018176/1Cancer Research UK FC001097Medical Research Council FC001097Medical Research Council G0900109Medical Research Council G0900278Medical Research Council MR/K011782/1NIAID NIH HHS R01 AI136511NIAID NIH HHS R21 AI142506Wellcome Trust FC001097
6 · The paper itself

Abstract

Kinesins are microtubule (MT)-based motors important in cell division, motility, polarity, and intracellular transport in many eukaryotes. However, they are poorly studied in the divergent eukaryotic pathogens Plasmodium spp., the causative agents of malaria, which manifest atypical aspects of cell division and plasticity of morphology throughout the life cycle in both mammalian and mosquito hosts. Here, we describe a genome-wide screen of Plasmodium kinesins, revealing diverse subcellular locations and functions in spindle assembly, axoneme formation, and cell morphology. Surprisingly, only kinesin-13 is essential for growth in the mammalian host while the other 8 kinesins are required during the proliferative and invasive stages of parasite transmission through the mosquito vector. In-depth analyses of kinesin-13 and kinesin-20 revealed functions in MT dynamics during apical cell polarity formation, spindle assembly, and axoneme biogenesis. These findings help us to understand the importance of MT motors and may be exploited to discover new therapeutic interventions against malaria.

Indexed as

CulicidaeMalariaParasitesPlasmodiumAnimalsHumansKinesinsLife Cycle StagesMammalsMicrotubulesKinesins

Identifiers

PMID35900985
PMCPMC9333250
OpenAlexW4288447344

What OpenQuestion holds

Textmetadata
LicenceCC0
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.