4.5 Article

Characterisation of a Rho homologue of Schistosoma mansoni

期刊

INTERNATIONAL JOURNAL FOR PARASITOLOGY
卷 33, 期 7, 页码 721-731

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ELSEVIER SCI LTD
DOI: 10.1016/S0020-7519(03)00046-8

关键词

Schistosoma mansoni; small GTPase; Rho; Rac; Cdc42; prenylation

资金

  1. NIAID NIH HHS [AI-46762, AI-41197, N01-AI-55270] Funding Source: Medline

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The development and survival of the helminth parasite, Schistosoma mansoni, is dependent on its ability to interpret signals from its environment. Currently, little is known about signal transduction in schistosomes. Rho is a member of a super-family of small GTP-binding proteins. Rho is involved in a number of cell signalling pathways with effects on actin cytoskeleton organisation, gene transcription, cell cycle progression, and membrane trafficking. We have cloned an S. mansoni protein (Rho1) that has 71-75% identity and similar to 85% similarity with human Rho A, B, and C proteins. We have optimised expression of recombinant S. mansoni Rho1 protein in Escherichia coli by co-expression with rare tRNAs. Western blot analysis results showed expression of Rho I protein in adult worm stages especially female worms. In vitro prenylation of recombinant S. mansoni Rho I determined that, similar to Rho from other organisms, Rho I is geranynlgeranylated but not farnesylated. A search of the gene database indicates that Rho GTPases exist as a small family in S. mansoni including orthologues of Rho, Cdc42, and Rac. These data suggest that S. mansoni Rho I plays a role in signalling in adult worms, especially females. (C) 2003 Australian Society for Parasitology Inc. Published by Elsevier Science Ltd. All rights reserved.

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