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Analysis of Tospovirus NSs Proteins in Suppression of Systemic Silencing

RNA silencing is a sequence-specific gene regulation mechanism that in plants also acts antiviral. In order to counteract antiviral RNA silencing, viruses have evolved RNA silencing suppressors (RSS). In the case of tospoviruses, the non-structural NSs protein has been identified as the RSS. Althoug...

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Autores principales: Hedil, Marcio, Sterken, Mark G., de Ronde, Dryas, Lohuis, Dick, Kormelink, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4537313/
https://www.ncbi.nlm.nih.gov/pubmed/26275304
http://dx.doi.org/10.1371/journal.pone.0134517
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author Hedil, Marcio
Sterken, Mark G.
de Ronde, Dryas
Lohuis, Dick
Kormelink, Richard
author_facet Hedil, Marcio
Sterken, Mark G.
de Ronde, Dryas
Lohuis, Dick
Kormelink, Richard
author_sort Hedil, Marcio
collection PubMed
description RNA silencing is a sequence-specific gene regulation mechanism that in plants also acts antiviral. In order to counteract antiviral RNA silencing, viruses have evolved RNA silencing suppressors (RSS). In the case of tospoviruses, the non-structural NSs protein has been identified as the RSS. Although the tomato spotted wilt virus (TSWV) tospovirus NSs protein has been shown to exhibit affinity to long and small dsRNA molecules, its ability to suppress the non-cell autonomous part of RNA silencing has only been studied to a limited extent. Here, the NSs proteins of TSWV, groundnut ringspot virus (GRSV) and tomato yellow ring virus (TYRV), representatives for three distinct tospovirus species, have been studied on their ability and strength to suppress local and systemic silencing. A system has been developed to quantify suppression of GFP silencing in Nicotiana benthamiana 16C lines, to allow a comparison of relative RNA silencing suppressor strength. It is shown that NSs of all three tospoviruses are suppressors of local and systemic silencing. Unexpectedly, suppression of systemic RNA silencing by NSs(TYRV) was just as strong as those by NSs(TSWV) and NSs(GRSV), even though NSs(TYRV) was expressed in lower amounts. Using the system established, a set of selected NSs(TSWV) gene constructs mutated in predicted RNA binding domains, as well as NSs from TSWV isolates 160 and 171 (resistance breakers of the Tsw resistance gene), were analyzed for their ability to suppress systemic GFP silencing. The results indicate another mode of RNA silencing suppression by NSs that acts further downstream the biogenesis of siRNAs and their sequestration. The findings are discussed in light of the affinity of NSs for small and long dsRNA, and recent mutant screen of NSs(TSWV) to map domains required for RSS activity and triggering of Tsw-governed resistance.
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spelling pubmed-45373132015-08-20 Analysis of Tospovirus NSs Proteins in Suppression of Systemic Silencing Hedil, Marcio Sterken, Mark G. de Ronde, Dryas Lohuis, Dick Kormelink, Richard PLoS One Research Article RNA silencing is a sequence-specific gene regulation mechanism that in plants also acts antiviral. In order to counteract antiviral RNA silencing, viruses have evolved RNA silencing suppressors (RSS). In the case of tospoviruses, the non-structural NSs protein has been identified as the RSS. Although the tomato spotted wilt virus (TSWV) tospovirus NSs protein has been shown to exhibit affinity to long and small dsRNA molecules, its ability to suppress the non-cell autonomous part of RNA silencing has only been studied to a limited extent. Here, the NSs proteins of TSWV, groundnut ringspot virus (GRSV) and tomato yellow ring virus (TYRV), representatives for three distinct tospovirus species, have been studied on their ability and strength to suppress local and systemic silencing. A system has been developed to quantify suppression of GFP silencing in Nicotiana benthamiana 16C lines, to allow a comparison of relative RNA silencing suppressor strength. It is shown that NSs of all three tospoviruses are suppressors of local and systemic silencing. Unexpectedly, suppression of systemic RNA silencing by NSs(TYRV) was just as strong as those by NSs(TSWV) and NSs(GRSV), even though NSs(TYRV) was expressed in lower amounts. Using the system established, a set of selected NSs(TSWV) gene constructs mutated in predicted RNA binding domains, as well as NSs from TSWV isolates 160 and 171 (resistance breakers of the Tsw resistance gene), were analyzed for their ability to suppress systemic GFP silencing. The results indicate another mode of RNA silencing suppression by NSs that acts further downstream the biogenesis of siRNAs and their sequestration. The findings are discussed in light of the affinity of NSs for small and long dsRNA, and recent mutant screen of NSs(TSWV) to map domains required for RSS activity and triggering of Tsw-governed resistance. Public Library of Science 2015-08-14 /pmc/articles/PMC4537313/ /pubmed/26275304 http://dx.doi.org/10.1371/journal.pone.0134517 Text en © 2015 Hedil et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hedil, Marcio
Sterken, Mark G.
de Ronde, Dryas
Lohuis, Dick
Kormelink, Richard
Analysis of Tospovirus NSs Proteins in Suppression of Systemic Silencing
title Analysis of Tospovirus NSs Proteins in Suppression of Systemic Silencing
title_full Analysis of Tospovirus NSs Proteins in Suppression of Systemic Silencing
title_fullStr Analysis of Tospovirus NSs Proteins in Suppression of Systemic Silencing
title_full_unstemmed Analysis of Tospovirus NSs Proteins in Suppression of Systemic Silencing
title_short Analysis of Tospovirus NSs Proteins in Suppression of Systemic Silencing
title_sort analysis of tospovirus nss proteins in suppression of systemic silencing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4537313/
https://www.ncbi.nlm.nih.gov/pubmed/26275304
http://dx.doi.org/10.1371/journal.pone.0134517
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