Plasmodium falciparum CRK4 links early mitotic events to the onset of S-phase during schizogony

Author:

Machado Marta12ORCID,Klaus Severina1ORCID,Klaschka Darius1,Guizetti Julien1ORCID,Ganter Markus1ORCID

Affiliation:

1. Center for Infectious Diseases, Heidelberg University Hospital , Heidelberg, Germany

2. Graduate Program in Areas of Basic and Applied Biology, Instituto de Ciências Biomédicas Abel Salazar, Universidade do Porto , Porto, Portugal

Abstract

ABSTRACT Plasmodium falciparum proliferates through schizogony in the clinically relevant blood stage of infection. During schizogony, consecutive rounds of DNA replication and nuclear division give rise to multinucleated stages before cellularization occurs. Although these nuclei reside in a shared cytoplasm, DNA replication and nuclear division occur asynchronously. Here, by mapping the proteomic context of the S-phase-promoting kinase Pf CRK4, we show that it has a dual role for nuclear-cycle progression: Pf CRK4 orchestrates not only DNA replication, but in parallel also the rearrangement of intranuclear microtubules from hemispindles into early mitotic spindles. Live-cell imaging of a reporter parasite showed that these microtubule rearrangements coincide with the onset of DNA replication. Together, our data render Pf CRK4 a key factor for nuclear-cycle progression, linking entry into S-phase with the initiation of mitotic events. In part, such links may compensate for the absence of canonical cell cycle checkpoints in P. falciparum . IMPORTANCE The human malaria parasite Plasmodium falciparum proliferates in erythrocytes through schizogony, forming multinucleated stages before cellularization occurs. In marked contrast to the pattern of proliferation seen in most model organisms, P. falciparum nuclei multiply asynchronously despite residing in a shared cytoplasm. This divergent mode of replication is, thus, a good target for therapeutic interventions. To exploit this potential, we investigated a key regulator of the parasite’s unusual cell cycle, the kinase Pf CRK4 and found that this kinase regulated not only DNA replication but also in parallel the rearrangement of nuclear microtubules into early mitotic spindles. Since canonical cell cycle checkpoints have not been described in P. falciparum parasites, linking entry into S-phase and the initiation of mitotic events via a kinase, may be an alternative means to exert control, which is typically achieved by checkpoints.

Funder

MEC | Fundação para a Ciência e a Tecnologia

Deutsche Forschungsgemeinschaft

Baden-Württemberg Stiftung

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Proteomic approaches for protein kinase substrate identification in Apicomplexa;Molecular and Biochemical Parasitology;2024-09

2. Post-Translational Modifications of Proteins of Malaria Parasites during the Life Cycle;International Journal of Molecular Sciences;2024-06-02

3. The molecular mechanisms driving Plasmodium cell division;Biochemical Society Transactions;2024-04-02

4. Cytoskeletal dynamics in parasites;Current Opinion in Cell Biology;2024-02

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