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Plasmodium falciparum NIMA-related kinase Pfnek-1: sex specificity and assessment of essentiality for the erythrocytic asexual cycle

Authors :
Dorin-semblat, Dominique
Schmitt, Sophie
Semblat, Jean-philippe
Sicard, Audrey
Reininger, Luc
Goldring, Dean
Patterson, Shelley
Quashie, Neils
Chakrabarti, Debopam
Meijer, Laurent
Doerig, Christian
Dorin-semblat, Dominique
Schmitt, Sophie
Semblat, Jean-philippe
Sicard, Audrey
Reininger, Luc
Goldring, Dean
Patterson, Shelley
Quashie, Neils
Chakrabarti, Debopam
Meijer, Laurent
Doerig, Christian
Source :
Microbiology-sgm (1350-0872) (Soc General Microbiology), 2011-10 , Vol. 157 , P. 2785-2794
Publication Year :
2011

Abstract

The Plasmodium falciparum kinome includes a family of four protein kinases (Pfnek-1 to -4) related to the NIMA (never-in-mitosis) family, members of which play important roles in mitosis and meiosis in eukaryotic cells. Only one of these, Pfnek-1, which we previously characterized at the biochemical level, is expressed in asexual parasites. The other three (Pfnek-2, -3 and -4) are expressed predominantly in gametocytes, and a role for nek-2 and nek-4 in meiosis has been documented. Here we show by reverse genetics that Pfnek-1 is required for completion of the asexual cycle in red blood cells and that its expression in gametocytes in detectable by immunofluorescence in male (but not in female) gametocytes, in contrast with Pfnek-2 and Pfnek-4. This indicates that the function of Pfnek-1 is non-redundant with those of the other members of the Pfnek family and identifies Pfnek-1 as a potential target for antimalarial chemotherapy. A medium-throughput screen of a small-molecule library provides proof of concept that recombinant Pfnek-1 can be used as a target in drug discovery.

Details

Database :
OAIster
Journal :
Microbiology-sgm (1350-0872) (Soc General Microbiology), 2011-10 , Vol. 157 , P. 2785-2794
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1286163408
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1099.mic.0.049023-0