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Exogenous RNAi mechanisms contribute to transcriptome adaptation by phased siRNA clusters in Paramecium
Extensive research has characterized distinct exogenous RNAi pathways interfering in gene expression during vegetative growth of the unicellular model ciliate Paramecium. However, role of RNAi in endogenous transcriptome regulation, and environmental adaptation is unknown. Here, we describe the firs...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6735861/ https://www.ncbi.nlm.nih.gov/pubmed/31251800 http://dx.doi.org/10.1093/nar/gkz553 |
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author | Karunanithi, Sivarajan Oruganti, Vidya Marker, Simone Rodriguez-Viana, Angela M Drews, Franziska Pirritano, Marcello Nordström, Karl Simon, Martin Schulz, Marcel H |
author_facet | Karunanithi, Sivarajan Oruganti, Vidya Marker, Simone Rodriguez-Viana, Angela M Drews, Franziska Pirritano, Marcello Nordström, Karl Simon, Martin Schulz, Marcel H |
author_sort | Karunanithi, Sivarajan |
collection | PubMed |
description | Extensive research has characterized distinct exogenous RNAi pathways interfering in gene expression during vegetative growth of the unicellular model ciliate Paramecium. However, role of RNAi in endogenous transcriptome regulation, and environmental adaptation is unknown. Here, we describe the first genome-wide profiling of endogenous sRNAs in context of different transcriptomic states (serotypes). We developed a pipeline to identify, and characterize 2602 siRNA producing clusters (SRCs). Our data show no evidence that SRCs produce miRNAs, and in contrast to other species, no preference for strand specificity of siRNAs. Interestingly, most SRCs overlap coding genes and a separate group show siRNA phasing along the entire open reading frame, suggesting that the mRNA transcript serves as a source for siRNAs. Integrative analysis of siRNA abundance and gene expression levels revealed surprisingly that mRNA and siRNA show negative as well as positive associations. Two RNA-dependent RNA Polymerase mutants, RDR1 and RDR2, show a drastic loss of siRNAs especially in phased SRCs accompanied with increased mRNA levels. Importantly, most SRCs depend on both RDRs, reminiscent to primary siRNAs in the RNAi against exogenous RNA, indicating mechanistic overlaps between exogenous and endogenous RNAi contributing to flexible transcriptome adaptation. |
format | Online Article Text |
id | pubmed-6735861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-67358612019-09-16 Exogenous RNAi mechanisms contribute to transcriptome adaptation by phased siRNA clusters in Paramecium Karunanithi, Sivarajan Oruganti, Vidya Marker, Simone Rodriguez-Viana, Angela M Drews, Franziska Pirritano, Marcello Nordström, Karl Simon, Martin Schulz, Marcel H Nucleic Acids Res Genomics Extensive research has characterized distinct exogenous RNAi pathways interfering in gene expression during vegetative growth of the unicellular model ciliate Paramecium. However, role of RNAi in endogenous transcriptome regulation, and environmental adaptation is unknown. Here, we describe the first genome-wide profiling of endogenous sRNAs in context of different transcriptomic states (serotypes). We developed a pipeline to identify, and characterize 2602 siRNA producing clusters (SRCs). Our data show no evidence that SRCs produce miRNAs, and in contrast to other species, no preference for strand specificity of siRNAs. Interestingly, most SRCs overlap coding genes and a separate group show siRNA phasing along the entire open reading frame, suggesting that the mRNA transcript serves as a source for siRNAs. Integrative analysis of siRNA abundance and gene expression levels revealed surprisingly that mRNA and siRNA show negative as well as positive associations. Two RNA-dependent RNA Polymerase mutants, RDR1 and RDR2, show a drastic loss of siRNAs especially in phased SRCs accompanied with increased mRNA levels. Importantly, most SRCs depend on both RDRs, reminiscent to primary siRNAs in the RNAi against exogenous RNA, indicating mechanistic overlaps between exogenous and endogenous RNAi contributing to flexible transcriptome adaptation. Oxford University Press 2019-09-05 2019-06-28 /pmc/articles/PMC6735861/ /pubmed/31251800 http://dx.doi.org/10.1093/nar/gkz553 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Genomics Karunanithi, Sivarajan Oruganti, Vidya Marker, Simone Rodriguez-Viana, Angela M Drews, Franziska Pirritano, Marcello Nordström, Karl Simon, Martin Schulz, Marcel H Exogenous RNAi mechanisms contribute to transcriptome adaptation by phased siRNA clusters in Paramecium |
title | Exogenous RNAi mechanisms contribute to transcriptome adaptation by phased siRNA clusters in Paramecium |
title_full | Exogenous RNAi mechanisms contribute to transcriptome adaptation by phased siRNA clusters in Paramecium |
title_fullStr | Exogenous RNAi mechanisms contribute to transcriptome adaptation by phased siRNA clusters in Paramecium |
title_full_unstemmed | Exogenous RNAi mechanisms contribute to transcriptome adaptation by phased siRNA clusters in Paramecium |
title_short | Exogenous RNAi mechanisms contribute to transcriptome adaptation by phased siRNA clusters in Paramecium |
title_sort | exogenous rnai mechanisms contribute to transcriptome adaptation by phased sirna clusters in paramecium |
topic | Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6735861/ https://www.ncbi.nlm.nih.gov/pubmed/31251800 http://dx.doi.org/10.1093/nar/gkz553 |
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