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siRNAs and piRNAs collaborate for transposon control in the two-spotted spider mite

RNAi has revolutionized genetic research, and is being commercialized as an insect pest control technology. Mechanisms exploited for this purpose are antiviral and therefore rapidly evolving. Ideally, RNAi will also be used for noninsect pests; however, differences in RNAi biology make this uncertai...

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Detalles Bibliográficos
Autores principales: Mondal, Mosharrof, Mansfield, Kody, Flynt, Alex
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6004056/
https://www.ncbi.nlm.nih.gov/pubmed/29678924
http://dx.doi.org/10.1261/rna.065839.118
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author Mondal, Mosharrof
Mansfield, Kody
Flynt, Alex
author_facet Mondal, Mosharrof
Mansfield, Kody
Flynt, Alex
author_sort Mondal, Mosharrof
collection PubMed
description RNAi has revolutionized genetic research, and is being commercialized as an insect pest control technology. Mechanisms exploited for this purpose are antiviral and therefore rapidly evolving. Ideally, RNAi will also be used for noninsect pests; however, differences in RNAi biology make this uncertain. Tetranychus urticae (two-spotted spider mite) is a destructive noninsect pest, which has a proclivity to develop pesticide resistance. Here we provide a comprehensive study of the endogenous RNAi pathways of spider mites to inform design of exogenous RNAi triggers. This effort revealed unexpected roles for small RNAs and novel genome surveillance pathways. Spider mites have an expanded RNAi machinery relative to insects, encoding RNA dependent RNA polymerase (Rdrp) and extra Piwi-class effectors. Through analyzing T. urticae transcriptome data we explored small RNA biogenesis, and discovered five siRNA loci that appear central to genome surveillance. These RNAs are expressed in the gonad, which we hypothesize to trigger production of piRNAs for control of transposable elements (TEs). This work highlights the need to investigate endogenous RNAi biology as lessons from model organisms may not hold in other species, impacting development of an RNAi strategy.
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spelling pubmed-60040562019-07-01 siRNAs and piRNAs collaborate for transposon control in the two-spotted spider mite Mondal, Mosharrof Mansfield, Kody Flynt, Alex RNA Report RNAi has revolutionized genetic research, and is being commercialized as an insect pest control technology. Mechanisms exploited for this purpose are antiviral and therefore rapidly evolving. Ideally, RNAi will also be used for noninsect pests; however, differences in RNAi biology make this uncertain. Tetranychus urticae (two-spotted spider mite) is a destructive noninsect pest, which has a proclivity to develop pesticide resistance. Here we provide a comprehensive study of the endogenous RNAi pathways of spider mites to inform design of exogenous RNAi triggers. This effort revealed unexpected roles for small RNAs and novel genome surveillance pathways. Spider mites have an expanded RNAi machinery relative to insects, encoding RNA dependent RNA polymerase (Rdrp) and extra Piwi-class effectors. Through analyzing T. urticae transcriptome data we explored small RNA biogenesis, and discovered five siRNA loci that appear central to genome surveillance. These RNAs are expressed in the gonad, which we hypothesize to trigger production of piRNAs for control of transposable elements (TEs). This work highlights the need to investigate endogenous RNAi biology as lessons from model organisms may not hold in other species, impacting development of an RNAi strategy. Cold Spring Harbor Laboratory Press 2018-07 /pmc/articles/PMC6004056/ /pubmed/29678924 http://dx.doi.org/10.1261/rna.065839.118 Text en © 2018 Mondal et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Report
Mondal, Mosharrof
Mansfield, Kody
Flynt, Alex
siRNAs and piRNAs collaborate for transposon control in the two-spotted spider mite
title siRNAs and piRNAs collaborate for transposon control in the two-spotted spider mite
title_full siRNAs and piRNAs collaborate for transposon control in the two-spotted spider mite
title_fullStr siRNAs and piRNAs collaborate for transposon control in the two-spotted spider mite
title_full_unstemmed siRNAs and piRNAs collaborate for transposon control in the two-spotted spider mite
title_short siRNAs and piRNAs collaborate for transposon control in the two-spotted spider mite
title_sort sirnas and pirnas collaborate for transposon control in the two-spotted spider mite
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6004056/
https://www.ncbi.nlm.nih.gov/pubmed/29678924
http://dx.doi.org/10.1261/rna.065839.118
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