posted on 2015-04-03, 00:00authored byAline Teichmann, Daiani
M. Vargas, Karina
M. Monteiro, Bruna V. Meneghetti, Cristine S. Dutra, Rodolfo Paredes, Norbel Galanti, Arnaldo Zaha, Henrique B. Ferreira
The 14-3-3 protein family of eukaryotic
regulators was studied
in Echinococcus granulosus, the causative
agent of cystic hydatid disease. These proteins mediate important
cellular processes in eukaryotes and are expected to play important
roles in parasite biology. Six isoforms of E. granulosus 14-3-3 genes and proteins (Eg14-3-3.1–6) were analyzed, and
their phylogenetic relationships were established with bona
fide 14-3-3 orthologous proteins from eukaryotic species.
Eg14-3-3 isoforms with previous evidence of expression (Eg14-3-3.1–4)
in E. granulosus pathogenic larval
stage (metacestode) were cloned, and recombinant proteins were used
for functional studies. These protein isoforms were detected in different
components of E. granulosus metacestode,
including interface components with the host. The roles that are played
by Eg14-3-3 proteins in parasite biology were inferred from the repertoires
of interacting proteins with each isoform, as assessed by gel overlay,
cross-linking, and affinity chromatography assays. A total of 95 Eg14-3-3
protein ligands were identified by mass spectrometry. Eg14-3-3 isoforms
have shared partners (44 proteins), indicating some overlapping functions;
however, they also bind exclusive partners (51 proteins), suggesting
Eg14-3-3 functional specialization. These ligand repertoires indicate
the involvement of Eg14-3-3 proteins in multiple biochemical pathways
in the E. granulosus metacestode and
note some degree of isoform specialization.