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Vol. 13, Issue 7, 2397-2409, July 2002


*Centre National de la Recherche Scientifique FRE 2383, Bâtiment CERMO, Université Joseph Fourier, Grenoble, France
38041; The intracellular parasite Toxoplasma gondii
develops within a nonfusogenic vacuole containing a network of
elongated nanotubules that form connections with the vacuolar
membrane. Parasite secretory proteins discharged from dense
granules (known as GRA proteins) decorate this intravacuolar network
after invasion. Herein, we show using specific gene knockout mutants,
that the unique nanotubule conformation of the network is induced by
the parasite secretory protein GRA2 and further stabilized by GRA6. The
vacuolar compartment generated by GRA2 knockout parasites was
dramatically disorganized, and the normally tubular network was
replaced by small aggregated material. The defect observed in
Centre National de la Recherche Scientifique
Unité Mixte Recherche 5539, Université Montpellier II,
Montpellier, 34095 France;
Laboratory of Molecular
Parasitology, Université Libre de Bruxelles, Gosselies, 6041 Belgium; and §Department of Molecular Microbiology,
Washington University School of Medicine, St. Louis, Missouri 63110
gra2 parasites was evident from the initial stages of
network formation when a prominent cluster of multilamellar vesicles
forms at a posterior invagination of the parasite. The secretory
protein GRA6 failed to localize properly to this posterior organizing
center in
gra2 cells, indicating that this early
conformation is essential to proper assembly of the network.
Construction of a
gra6 mutant also led to an altered mature network characterized by small vesicles instead of elongated nanotubules; however, the initial formation of the posterior organizing center was normal. Complementation of the
gra2
knockout with mutated forms of GRA2 showed that the integrity of both
amphipathic alpha-helices of the protein is required for correct
formation of the network. The induction of nanotubues by the parasite
protein GRA2 may be a conserved feature of amphipathic alpha-helical
regions, which have also been implicated in the organization of Golgi
nanotubules and endocytic vesicles in mammalian cells.
Corresponding author. E-mail address:
marie-france.cesbron{at}ujf-grenoble.fr.
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