Mimicry of a G protein mutation by pertussis toxin expression in transgenic Caenorhabditis elegans.

Abstract:

:Pathogens produce virulence factors that interact directly with host molecules, but in many cases the host targets are unknown. The genetic and molecular identification of these orphan targets is often not feasible with mammalian experimental models. However, a substantial number of known targets are molecules and pathways that are conserved among eukaryotes, and therefore the use of nonmammalian model hosts to identify orphan targets may prove useful. To demonstrate the feasibility of this approach, we transformed the nematode Caenorhabditis elegans with a gene encoding the catalytic subunit of pertussis toxin (PTX), which in mammals inactivates G(o/i)alpha proteins. Expression of PTX in C. elegans produced phenotypes almost identical to those of a null mutation in the nematode gene encoding G(o/i)alpha. Furthermore, PTX suppressed the phenotype of a constitutively active form of nematode G(o/i)alpha protein. These results indicate that PTX is functional in nematodes and acts specifically on the C. elegans homologue of the mammalian target.

journal_name

Infect Immun

journal_title

Infection and immunity

authors

Darby C,Falkow S

doi

10.1128/IAI.69.10.6271-6275.2001

keywords:

subject

Has Abstract

pub_date

2001-10-01 00:00:00

pages

6271-5

issue

10

eissn

0019-9567

issn

1098-5522

journal_volume

69

pub_type

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