Luo S, Vieira M, Graves J, Zhong L, Moreno S N
Laboratory of Molecular Parasitology, Department of Pathobiology, University of Illinois at Urbana-Champaign, 2001 South Lincoln Avenue, Urbana, IL 61802, USA.
EMBO J. 2001 Jan 15;20(1-2):55-64. doi: 10.1093/emboj/20.1.55.
Ca(2+)-ATPases are likely to play critical roles in the biochemistry of Toxoplasma gondii, since these protozoa are obligate intracellular parasites and the Ca(2+) concentration in their intracellular location is three orders of magnitude lower than in the extracellular medium. Here, we report the cloning and sequencing of a gene encoding a plasma membrane-type Ca(2+)-ATPase (PMCA) of T.gondii (TgA1). The predicted protein (TgA1) exhibits 32-36% identity to vacuolar Ca(2+)-ATPases of Trypanosoma cruzi, Saccharomyces cerevisiae, Entamoeba histolytica and Dictyostelium discoideum. Sequencing of both cDNA and genomic DNA from T.gondii indicated that TgA1 contains two introns near the C-terminus. A hydropathy profile of the protein suggests 10 transmembrane domains. TgA1 suppresses the Ca(2+) hypersensitivity of a mutant of S.cerevisiae that has a defect in vacuolar Ca(2+) accumulation. Indirect immunofluorescence and immunoelectron microscopy analysis indicate that TgA1 localizes to the plasma membrane and co-localizes with the vacuolar H(+)-pyrophosphatase to intracellular vacuoles identified morphologically and by X-ray microanalysis as the acidocalcisomes. This vacuolar-type Ca(2+)-ATPase could play an important role in Ca(2+) homeostasis in T.gondii.
钙(2+)-ATP酶可能在刚地弓形虫的生物化学过程中发挥关键作用,因为这些原生动物是专性细胞内寄生虫,其细胞内位置的钙(2+)浓度比细胞外培养基中的低三个数量级。在此,我们报告了编码刚地弓形虫质膜型钙(2+)-ATP酶(PMCA)(TgA1)的基因的克隆和测序。预测的蛋白质(TgA1)与克氏锥虫、酿酒酵母、溶组织内阿米巴和盘基网柄菌的液泡钙(2+)-ATP酶具有32-36%的同一性。对来自刚地弓形虫的cDNA和基因组DNA进行测序表明,TgA1在C端附近含有两个内含子。该蛋白质的亲水性图谱表明有10个跨膜结构域。TgA1抑制了液泡钙(2+)积累存在缺陷的酿酒酵母突变体的钙(2+)超敏性。间接免疫荧光和免疫电子显微镜分析表明,TgA1定位于质膜,并与液泡H(+)-焦磷酸酶共定位于通过形态学和X射线微分析鉴定为酸性钙小体的细胞内液泡。这种液泡型钙(2+)-ATP酶可能在刚地弓形虫的钙(2+)稳态中发挥重要作用。