Abstract

Casein kinase 2 (CK2) is a pleiotropic kinase phosphorylating substrates in different cellular compartments in eukaryotes. In the malaria parasite Plasmodium falciparum, PfCK2 is vital for asexual proliferation of blood-stage parasites. Here, we applied CRISPR/Cas9-based gene editing to investigate the function of the PfCK2α catalytic subunit in gametocytes, the sexual forms of the parasite that are essential for malaria transmission. We show that PfCK2α localizes to the nucleus and cytoplasm in asexual and sexual parasites alike. Conditional knockdown of PfCK2α expression prevented the transition of stage IV into transmission-competent stage V gametocytes, whereas the conditional knockout of pfck2a completely blocked gametocyte maturation already at an earlier stage of sexual differentiation. In summary, our results demonstrate that PfCK2α is not only essential for asexual but also sexual development of P. falciparum blood-stage parasites and encourage studies exploring PfCK2α as a potential target for dual-active antimalarial drugs.

Highlights

  • The casein kinase CK2 has been implicated in the phosphorylation of a variety of substrates and executes essential cellular functions[17,22,23,24]

  • In P. falciparum PfCK2 is suggested to phosphorylate a broad range of substrates[10,31,32] and both the regulatory and catalytic kinase subunits are essential for asexual parasite development[10,12,32]

  • In order to study the function of the catalytic subunit PfCK2α in asexual and sexual development, we generated several transgenic parasites lines using CRISPR/Cas9-based gene editing

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Summary

Objectives

Because one of our aims was to test if PfCK2α has a role in regulating sexual commitment, the PfCK2αGFP and PfCK2α-GFPDD transgenic lines were generated in NF54 parasites expressing a mScarlet-tagged version of PfAP2-G (NF54/AP2-G-mScarlet) (Brancucci et al, manuscript in preparation)

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