Department of Infectious, Parasitic and Immunomediated Diseases, Istituto Superiore di Sanità, 00161 Rome, Italy.
J Proteome Res. 2012 May 4;11(5):2666-83. doi: 10.1021/pr3000199. Epub 2012 Apr 11.
14-3-3s are phosphoserine/phosphotreonine binding proteins that play pivotal roles as regulators of multiple cellular processes in eukaryotes. The flagellated protozoan parasite Giardia duodenalis, the causing agent of giardiasis, is a valuable simplified eukaryotic model. A single 14-3-3 isoform (g14-3-3) is expressed in Giardia, and it is directly involved in the differentiation of the parasite into cyst. To define the overall functions of g14-3-3, the protein interactome has been investigated. A transgenic G. duodenalis strain was engineered to express a FLAG-tagged g14-3-3 under its own promoter. Affinity chromatography coupled with tandem mass spectrometry analysis have been used to purify and identify FLAG-g14-3-3-associated proteins from trophozoites and encysting parasites. A total of 314 putative g14-3-3 interaction partners were identified, including proteins involved in several pathways. Some interactions seemed to be peculiar of one specific stage, while others were shared among the different stages. Furthermore, the interaction of g14-3-3 with the giardial homologue of the CDC7 protein kinase (gCDC7) was characterized, leading to the identification of a multiprotein complex containing not only g14-3-3 and gCDC7 but also a newly identified and highly divergent homologue of DBF4, the putative regulatory subunit of gCDC7. The relevance of g14-3-3 interactions in G. duodenalis biology was discussed.
14-3-3s 是磷酸丝氨酸/磷酸苏氨酸结合蛋白,在真核生物中作为多种细胞过程的调节剂发挥着关键作用。有鞭毛的原生动物寄生虫贾第虫(引起贾第虫病的病原体)是一个有价值的简化真核模型。贾第虫只表达一种 14-3-3 同工型(g14-3-3),它直接参与寄生虫向囊的分化。为了确定 g14-3-3 的整体功能,研究了蛋白质相互作用组。通过工程化将一个表达 FLAG 标签的 g14-3-3 的转基因 G. duodenalis 株在其自身启动子的控制下表达。亲和层析与串联质谱分析已被用于从滋养体和囊形成寄生虫中纯化和鉴定 FLAG-g14-3-3 相关蛋白。共鉴定了 314 种推定的 g14-3-3 相互作用伙伴,包括参与几种途径的蛋白质。一些相互作用似乎是特定阶段特有的,而另一些则在不同阶段共享。此外,还对 g14-3-3 与 CDC7 蛋白激酶(gCDC7)的贾第虫同源物的相互作用进行了表征,导致鉴定了一个包含不仅 g14-3-3 和 gCDC7 而且还包含一个新鉴定的高度分化的 DBF4 同源物的多蛋白复合物,DBF4 是 gCDC7 的假定调节亚基。讨论了 g14-3-3 相互作用在 G. duodenalis 生物学中的相关性。