Interaction Network of the 14-3-3 Protein in the Ancient Protozoan Parasite Giardia duodenalis

被引:30
|
作者
Lalle, Marco [1 ]
Camerini, Serena [2 ]
Cecchetti, Serena [2 ]
Sayadi, Ahmed [3 ]
Crescenzi, Marco [2 ]
Pozio, Edoardo [1 ]
机构
[1] Ist Super Sanita, Dept Infect Parasit & Immunomediated Dis, I-00161 Rome, Italy
[2] Ist Super Sanita, Dept Cell Biol & Neurosci, I-00161 Rome, Italy
[3] Univ Rome Sapienza, Dept Biochem Sci A Rossi Fanelli, I-00185 Rome, Italy
关键词
14-3-3; protein; protein-protein interaction; Giardia duodenalis; encystation; gCDC7; CYCLIN-DEPENDENT KINASES; PROTEOMIC ANALYSIS; SACCHAROMYCES-CEREVISIAE; SECRETORY APPARATUS; CRYSTAL-STRUCTURES; CYST WALL; LAMBLIA; BINDING; PHOSPHORYLATION; INTESTINALIS;
D O I
10.1021/pr3000199
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:2666 / 2683
页数:18
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