Hortua Triana Miryam A, Márquez-Nogueras Karla M, Chang Le, Stasic Andrew J, Li Catherine, Spiegel Kevin A, Sharma Amrita, Li Zhu-Hong, Moreno Silvia N J
Center for Tropical and Emerging Global Diseases, University of Georgia, Athens, Georgia, 30602.
Department of Cellular Biology, University of Georgia, Athens, Georgia, 30602.
J Eukaryot Microbiol. 2018 Jul;65(5):709-721. doi: 10.1111/jeu.12626. Epub 2018 May 11.
Calcium ions regulate a diversity of cellular functions in all eukaryotes. The cytosolic Ca concentration is tightly regulated at the physiological cytosolic concentration of 50-100 nm. The Toxoplasma gondii genome predicts the presence of several genes encoding potential Ca channels, pumps, and transporters. Many of these genes are weakly expressed and likely tightly regulated due to their potential impact to the physiology of the cell. Endogenous tagging has been widely used to localize proteins in T. gondii but low level of expression of many of them makes visualization of tags difficult and sometimes impossible. The use of high-performance tags for labeling proteins expressed at low level is ideal for investigating the localization of these gene products. We designed a Carboxy-terminus tagging plasmid containing the previously characterized "spaghetti monster-HA" (smHA) or "spaghetti monster-MYC" (smMYC) tags. These tags consist of 10 copies of a single epitope (HA or MYC) inserted into a darkened green fluorescence protein scaffold. We localized six proteins of various levels of expression. Clonal lines were isolated and validated by PCR, western blot, and immunofluorescence analyses. Some gene products were only visible when tagged with smHA and in one case the smHA revealed a novel localization previously undetected.
钙离子调节所有真核生物中多种细胞功能。胞质钙浓度在50 - 100纳米的生理胞质浓度下受到严格调控。刚地弓形虫基因组预测存在几个编码潜在钙通道、泵和转运蛋白的基因。这些基因中的许多表达较弱,由于它们对细胞生理的潜在影响,可能受到严格调控。内源性标记已被广泛用于在刚地弓形虫中定位蛋白质,但其中许多蛋白质的低表达水平使得标记的可视化变得困难,有时甚至无法实现。使用高性能标签标记低水平表达的蛋白质非常适合研究这些基因产物的定位。我们设计了一种羧基末端标记质粒,其中包含先前表征的“意大利面条怪物 - HA”(smHA)或“意大利面条怪物 - MYC”(smMYC)标签。这些标签由插入深绿色荧光蛋白支架中的10个单一表位(HA或MYC)拷贝组成。我们定位了六种不同表达水平的蛋白质。通过PCR、western印迹和免疫荧光分析分离并验证了克隆系。一些基因产物只有在用smHA标记时才能看到,在一个案例中,smHA揭示了一个以前未检测到的新定位。