protein phosphorylation during sexual differentiation in the malaria parasite plasmodium falciparum

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Molecular and Biochemical Parasitology 87 (1997) 205 – 210 Short communication Protein phosphorylation during sexual differentiation in the malaria parasite Plasmodium falciparum Nirbhay Kumar * Department of Molecular Microbiology and Immunology, Johns Hopkins School of Public Health, 615 N. Wolfe Street, Baltimore, MD 21205, USA Received 28 February 1997; received in revised form 1 April 1997; accepted 3 April 1997 Keywords: Plasmodium falciparum; Malaria; Sexual stages; Phosphorylation; Pfg27 The unicellular protozoan parasites belonging to the genus Plasmodium have a complex life cycle in which the asexual multiplication of parasites in the vertebrate host alternates with an obligate sexual reproduction in the mosquito vector. Ery- throcytic sexual stages (male and female gameto- cytes) are produced by sexual differentiation of asexual stages within the vertebrate host and are responsible for transmitting the parasite to the mosquito vector. The sexual reproduction of the parasites in the mosquitoes involves a complex set of events leading to the formation of extracellular female and motile male gametes, which undergo fertilization and further development [1]. It is during the mating between male and female gametes that genetic recombination occurs during meiotic division of fertilized zygotes. Mating is also believed to be a major factor contributing to enormous genetic diversity of the parasite popula- tion [2]. Such diverse parasites are then dissemi- nated into the human population during further transmission. Sexual differentiation and develop- ment of the malaria parasite thus occupies a central place in the biology of this parasite which poses a major health risk worldwide. The initiation of sexual differentiation occurs early during invasion of erythrocytes by mero- zoites. A clonal population of haploid parasites can generate both male and female gametocytes. Sexually differentiated parasites undergo pro- found morphological, biochemical and functional changes. These are accompanied by preferential expression of a number of proteins in a coordi- nated fashion during distinct maturation stages of gametocytes defined as stages I–V [3–5]. Pfg27 (Mr 27 000) is one such cytoplasmic protein abun- Abbre6iations: SDS-PAGE, sodium dodecyl sulfate-poly- acrylamide gel electrophoresis; TLC, thin layer chromatogra- phy. * Tel.: +1 410 9557177; fax: +1 410 9550105; e-mail: [email protected] 0166-6851/97/$17.00 © 1997 Elsevier Science B.V. All rights reserved. PII S0166-6851(97)00051-0

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Page 1: Protein phosphorylation during sexual differentiation in the malaria parasite Plasmodium falciparum

Molecular and Biochemical Parasitology 87 (1997) 205–210

Short communication

Protein phosphorylation during sexual differentiation in themalaria parasite Plasmodium falciparum

Nirbhay Kumar *

Department of Molecular Microbiology and Immunology, Johns Hopkins School of Public Health, 615 N. Wolfe Street, Baltimore,MD 21205, USA

Received 28 February 1997; received in revised form 1 April 1997; accepted 3 April 1997

Keywords: Plasmodium falciparum ; Malaria; Sexual stages; Phosphorylation; Pfg27

The unicellular protozoan parasites belongingto the genus Plasmodium have a complex life cyclein which the asexual multiplication of parasites inthe vertebrate host alternates with an obligatesexual reproduction in the mosquito vector. Ery-throcytic sexual stages (male and female gameto-cytes) are produced by sexual differentiation ofasexual stages within the vertebrate host and areresponsible for transmitting the parasite to themosquito vector. The sexual reproduction of theparasites in the mosquitoes involves a complex setof events leading to the formation of extracellularfemale and motile male gametes, which undergofertilization and further development [1]. It isduring the mating between male and female

gametes that genetic recombination occurs duringmeiotic division of fertilized zygotes. Mating isalso believed to be a major factor contributing toenormous genetic diversity of the parasite popula-tion [2]. Such diverse parasites are then dissemi-nated into the human population during furthertransmission. Sexual differentiation and develop-ment of the malaria parasite thus occupies acentral place in the biology of this parasite whichposes a major health risk worldwide.

The initiation of sexual differentiation occursearly during invasion of erythrocytes by mero-zoites. A clonal population of haploid parasitescan generate both male and female gametocytes.Sexually differentiated parasites undergo pro-found morphological, biochemical and functionalchanges. These are accompanied by preferentialexpression of a number of proteins in a coordi-nated fashion during distinct maturation stages ofgametocytes defined as stages I–V [3–5]. Pfg27(Mr 27 000) is one such cytoplasmic protein abun-

Abbre6iations: SDS-PAGE, sodium dodecyl sulfate-poly-acrylamide gel electrophoresis; TLC, thin layer chromatogra-phy.

* Tel.: +1 410 9557177; fax: +1 410 9550105; e-mail:[email protected]

0166-6851/97/$17.00 © 1997 Elsevier Science B.V. All rights reserved.

PII S 0 1 66 -6851 (97 )00051 -0

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