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Systemic RNAi mediated gene silencing in the anhydrobiotic nematode Panagrolaimus superbus

BACKGROUND: Gene silencing by RNA interference (RNAi) is a powerful tool for functional genomics. Although RNAi was first described in Caenorhabditis elegans, several nematode species are unable to mount an RNAi response when exposed to exogenous double stranded RNA (dsRNA). These include the satell...

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Autores principales: Shannon, Adam J, Tyson, Trevor, Dix, Ilona, Boyd, Jacqueline, Burnell, Ann M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2453295/
https://www.ncbi.nlm.nih.gov/pubmed/18565215
http://dx.doi.org/10.1186/1471-2199-9-58
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author Shannon, Adam J
Tyson, Trevor
Dix, Ilona
Boyd, Jacqueline
Burnell, Ann M
author_facet Shannon, Adam J
Tyson, Trevor
Dix, Ilona
Boyd, Jacqueline
Burnell, Ann M
author_sort Shannon, Adam J
collection PubMed
description BACKGROUND: Gene silencing by RNA interference (RNAi) is a powerful tool for functional genomics. Although RNAi was first described in Caenorhabditis elegans, several nematode species are unable to mount an RNAi response when exposed to exogenous double stranded RNA (dsRNA). These include the satellite model organisms Pristionchus pacificus and Oscheius tipulae. Available data also suggest that the RNAi pathway targeting exogenous dsRNA may not be fully functional in some animal parasitic nematodes. The genus Panagrolaimus contains bacterial feeding nematodes which occupy a diversity of niches ranging from polar, temperate and semi-arid soils to terrestrial mosses. Thus many Panagrolaimus species are adapted to tolerate freezing and desiccation and are excellent systems to study the molecular basis of environmental stress tolerance. We investigated whether Panagrolaimus is susceptible to RNAi to determine whether this nematode could be used in large scale RNAi studies in functional genomics. RESULTS: We studied two species: Panagrolaimus sp. PS1159 and Panagrolaimus superbus. Both nematode species displayed embryonic lethal RNAi phenotypes following ingestion of Escherichia coli expressing dsRNA for the C. elegans embryonic lethal genes Ce-lmn-1 and Ce-ran-4. Embryonic lethal RNAi phenotypes were also obtained in both species upon ingestion of dsRNA for the Panagrolaimus genes ef1b and rps-2. Single nematode RT-PCR showed that a significant reduction in mRNA transcript levels occurred for the target ef1b and rps-2 genes in RNAi treated Panagrolaimus sp. 1159 nematodes. Visible RNAi phenotypes were also observed when P. superbus was exposed to dsRNA for structural genes encoding contractile proteins. All RNAi phenotypes were highly penetrant, particularly in P. superbus. CONCLUSION: This demonstration that Panagrolaimus is amenable to RNAi by feeding will allow the development of high throughput methods of RNAi screening for P. superbus. This greatly enhances the utility of this nematode as a model system for the study of the molecular biology of anhydrobiosis and cryobiosis and as a possible satellite model nematode for comparative and functional genomics. Our data also identify another nematode infraorder which is amenable to RNAi and provide additional information on the diversity of RNAi phenotypes in nematodes.
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spelling pubmed-24532952008-07-12 Systemic RNAi mediated gene silencing in the anhydrobiotic nematode Panagrolaimus superbus Shannon, Adam J Tyson, Trevor Dix, Ilona Boyd, Jacqueline Burnell, Ann M BMC Mol Biol Research Article BACKGROUND: Gene silencing by RNA interference (RNAi) is a powerful tool for functional genomics. Although RNAi was first described in Caenorhabditis elegans, several nematode species are unable to mount an RNAi response when exposed to exogenous double stranded RNA (dsRNA). These include the satellite model organisms Pristionchus pacificus and Oscheius tipulae. Available data also suggest that the RNAi pathway targeting exogenous dsRNA may not be fully functional in some animal parasitic nematodes. The genus Panagrolaimus contains bacterial feeding nematodes which occupy a diversity of niches ranging from polar, temperate and semi-arid soils to terrestrial mosses. Thus many Panagrolaimus species are adapted to tolerate freezing and desiccation and are excellent systems to study the molecular basis of environmental stress tolerance. We investigated whether Panagrolaimus is susceptible to RNAi to determine whether this nematode could be used in large scale RNAi studies in functional genomics. RESULTS: We studied two species: Panagrolaimus sp. PS1159 and Panagrolaimus superbus. Both nematode species displayed embryonic lethal RNAi phenotypes following ingestion of Escherichia coli expressing dsRNA for the C. elegans embryonic lethal genes Ce-lmn-1 and Ce-ran-4. Embryonic lethal RNAi phenotypes were also obtained in both species upon ingestion of dsRNA for the Panagrolaimus genes ef1b and rps-2. Single nematode RT-PCR showed that a significant reduction in mRNA transcript levels occurred for the target ef1b and rps-2 genes in RNAi treated Panagrolaimus sp. 1159 nematodes. Visible RNAi phenotypes were also observed when P. superbus was exposed to dsRNA for structural genes encoding contractile proteins. All RNAi phenotypes were highly penetrant, particularly in P. superbus. CONCLUSION: This demonstration that Panagrolaimus is amenable to RNAi by feeding will allow the development of high throughput methods of RNAi screening for P. superbus. This greatly enhances the utility of this nematode as a model system for the study of the molecular biology of anhydrobiosis and cryobiosis and as a possible satellite model nematode for comparative and functional genomics. Our data also identify another nematode infraorder which is amenable to RNAi and provide additional information on the diversity of RNAi phenotypes in nematodes. BioMed Central 2008-06-19 /pmc/articles/PMC2453295/ /pubmed/18565215 http://dx.doi.org/10.1186/1471-2199-9-58 Text en Copyright © 2008 Shannon et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Shannon, Adam J
Tyson, Trevor
Dix, Ilona
Boyd, Jacqueline
Burnell, Ann M
Systemic RNAi mediated gene silencing in the anhydrobiotic nematode Panagrolaimus superbus
title Systemic RNAi mediated gene silencing in the anhydrobiotic nematode Panagrolaimus superbus
title_full Systemic RNAi mediated gene silencing in the anhydrobiotic nematode Panagrolaimus superbus
title_fullStr Systemic RNAi mediated gene silencing in the anhydrobiotic nematode Panagrolaimus superbus
title_full_unstemmed Systemic RNAi mediated gene silencing in the anhydrobiotic nematode Panagrolaimus superbus
title_short Systemic RNAi mediated gene silencing in the anhydrobiotic nematode Panagrolaimus superbus
title_sort systemic rnai mediated gene silencing in the anhydrobiotic nematode panagrolaimus superbus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2453295/
https://www.ncbi.nlm.nih.gov/pubmed/18565215
http://dx.doi.org/10.1186/1471-2199-9-58
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