Disruption of Plasmodium falciparum kinetochore proteins destabilises the nexus between the centrosome equivalent and the mitotic apparatus

Plasmodium falciparum is the causative agent of malaria and remains a pathogen of global importance. Asexual blood stage replication, via a process called schizogony, is an important target for the development of new antimalarials. Here we use ultrastructure-expansion microscopy to probe the organis...

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Vydané v:Nature communications Ročník 15; číslo 1; s. 5794 - 16
Hlavní autori: Li, Jiahong, Shami, Gerald J., Liffner, Benjamin, Cho, Ellie, Braet, Filip, Duraisingh, Manoj T., Absalon, Sabrina, Dixon, Matthew W. A., Tilley, Leann
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: London Nature Publishing Group UK 10.07.2024
Nature Publishing Group
Nature Portfolio
Predmet:
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Centromere - metabolism
Centromeres
Centrosome - metabolism
Developmental stages
Disruption
Equivalence
Humanities and Social Sciences
Humans
Kinetochores
Kinetochores - metabolism
Malaria
Malaria, Falciparum - metabolism
Malaria, Falciparum - parasitology
Merozoites
Merozoites - metabolism
Merozoites - physiology
Microscopy
Mitosis
multidisciplinary
Nuclear Envelope - metabolism
Nuclei
Organelles
Parasites
Plasmodium falciparum
Plasmodium falciparum - metabolism
Plasmodium falciparum - physiology
Protozoan Proteins - genetics
Protozoan Proteins - metabolism
Schizogony
Science
Science (multidisciplinary)
Spindle Apparatus - metabolism
Ultrastructure
Vector-borne diseases
ISSN:2041-1723, 2041-1723
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Shrnutí:Plasmodium falciparum is the causative agent of malaria and remains a pathogen of global importance. Asexual blood stage replication, via a process called schizogony, is an important target for the development of new antimalarials. Here we use ultrastructure-expansion microscopy to probe the organisation of the chromosome-capturing kinetochores in relation to the mitotic spindle, the centriolar plaque, the centromeres and the apical organelles during schizont development. Conditional disruption of the kinetochore components, Pf NDC80 and Pf Nuf2, is associated with aberrant mitotic spindle organisation, disruption of the centromere marker, CENH3 and impaired karyokinesis. Surprisingly, kinetochore disruption also leads to disengagement of the centrosome equivalent from the nuclear envelope. Severing the connection between the nucleus and the apical complex leads to the formation of merozoites lacking nuclei. Here, we show that correct assembly of the kinetochore/spindle complex plays a previously unrecognised role in positioning the nascent apical complex in developing P. falciparum merozoites. Using Ultra-Expansion Microscopy of the malaria parasite, P. falciparum , Li et al. show that disruption of kinetochore components breaks a nexus between the mitotic spindle and the nascent apical organelles.
Bibliografia:ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-024-50167-6