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PMID: 18545708 Published · epublish English Journal Article

Deciphering the ubiquitin-mediated pathway in apicomplexan parasites: a potential strategy to interfere with parasite virulence.

PloS one ·Vol. 3 ·No. 6 ·2008-06-11 ·Pages e2386

Ponts N, Yang J, Chung DW, Prudhomme J, Girke T, Horrocks P, Le Roch KG

Abstract

Reversible modification of proteins through the attachment of ubiquitin or ubiquitin-like modifiers is an essential post-translational regulatory mechanism in eukaryotes. The conjugation of ubiquitin or ubiquitin-like proteins has been demonstrated to play roles in growth, adaptation and homeostasis in all eukaryotes, with perturbation of ubiquitin-mediated systems associated with the pathogenesis of many human diseases, including cancer and neurodegenerative disorders. Here we describe the use of an HMM search of functional Pfam domains found in the key components of the ubiquitin-mediated pathway necessary to activate and reversibly modify target proteins in eight apicomplexan parasitic protozoa for which complete or late-stage genome projects exist. In parallel, the same search was conducted on five model organisms, single-celled and metazoans, to generate data to validate both the search parameters employed and aid paralog classification in Apicomplexa. For each of the 13 species investigated, a set of proteins predicted to be involved in the ubiquitylation pathway has been identified and demonstrates increasing component members of the ubiquitylation pathway correlating with organism and genome complexity. Sequence homology and domain architecture analyses facilitated prediction of apicomplexan-specific protein function, particularly those involved in regulating cell division during these parasite's complex life cycles. This study provides a comprehensive analysis of proteins predicted to be involved in the apicomplexan ubiquitin-mediated pathway. Given the importance of such pathway in a wide variety of cellular processes, our data is a key step in elucidating the biological networks that, in part, direct the pathogenicity of these parasites resulting in a massive impact on global health. Moreover, apicomplexan-specific adaptations of the ubiquitylation pathway may represent new therapeutic targets for much needed drugs against apicomplexan parasites.

MeSH Terms
Animals Apicomplexa/parasitology Eukaryota/classification,pathogenicity Species Specificity Ubiquitin/metabolism
Chemicals
Ubiquitin
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Ponts Nadia
Department of Cell Biology and Neurosciences, University of California at Riverside, Riverside, California, United States of America.
Yang Jianfeng
Chung Duk-Won Doug
Prudhomme Jacques
Girke Thomas
Horrocks Paul
Le Roch Karine G
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Article Info
Journal
PloS one
Abbr.
PLoS One
ISSN
1932-6203
Published
2008-06-11
Epub
2008-00-11
Pages
e2386
Language
English
Region
United States
NLM ID
101285081
PMCID
PMC2408969
Subset
IM
Analysis Services
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