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Landscape of the spliced leader trans-splicing mechanism in Schistosoma mansoni

Spliced leader dependent trans-splicing (SLTS) has been described as an important RNA regulatory process that occurs in different organisms, including the trematode Schistosoma mansoni. We identified more than seven thousand putative SLTS sites in the parasite, comprising genes with a wide spectrum...

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Autores principales: Boroni, Mariana, Sammeth, Michael, Gava, Sandra Grossi, Jorge, Natasha Andressa Nogueira, Macedo, Andréa Mara, Machado, Carlos Renato, Mourão, Marina Moraes, Franco, Glória Regina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832876/
https://www.ncbi.nlm.nih.gov/pubmed/29497070
http://dx.doi.org/10.1038/s41598-018-22093-3
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author Boroni, Mariana
Sammeth, Michael
Gava, Sandra Grossi
Jorge, Natasha Andressa Nogueira
Macedo, Andréa Mara
Machado, Carlos Renato
Mourão, Marina Moraes
Franco, Glória Regina
author_facet Boroni, Mariana
Sammeth, Michael
Gava, Sandra Grossi
Jorge, Natasha Andressa Nogueira
Macedo, Andréa Mara
Machado, Carlos Renato
Mourão, Marina Moraes
Franco, Glória Regina
author_sort Boroni, Mariana
collection PubMed
description Spliced leader dependent trans-splicing (SLTS) has been described as an important RNA regulatory process that occurs in different organisms, including the trematode Schistosoma mansoni. We identified more than seven thousand putative SLTS sites in the parasite, comprising genes with a wide spectrum of functional classes, which underlines the SLTS as a ubiquitous mechanism in the parasite. Also, SLTS gene expression levels span several orders of magnitude, showing that SLTS frequency is not determined by the expression level of the target gene, but by the presence of particular gene features facilitating or hindering the trans-splicing mechanism. Our in-depth investigation of SLTS events demonstrates widespread alternative trans-splicing (ATS) acceptor sites occurring in different regions along the entire gene body, highlighting another important role of SLTS generating alternative RNA isoforms in the parasite, besides the polycistron resolution. Particularly for introns where SLTS directly competes for the same acceptor substrate with cis-splicing, we identified for the first time additional and important features that might determine the type of splicing. Our study substantially extends the current knowledge of RNA processing by SLTS in S. mansoni, and provide basis for future studies on the trans-splicing mechanism in other eukaryotes.
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spelling pubmed-58328762018-03-05 Landscape of the spliced leader trans-splicing mechanism in Schistosoma mansoni Boroni, Mariana Sammeth, Michael Gava, Sandra Grossi Jorge, Natasha Andressa Nogueira Macedo, Andréa Mara Machado, Carlos Renato Mourão, Marina Moraes Franco, Glória Regina Sci Rep Article Spliced leader dependent trans-splicing (SLTS) has been described as an important RNA regulatory process that occurs in different organisms, including the trematode Schistosoma mansoni. We identified more than seven thousand putative SLTS sites in the parasite, comprising genes with a wide spectrum of functional classes, which underlines the SLTS as a ubiquitous mechanism in the parasite. Also, SLTS gene expression levels span several orders of magnitude, showing that SLTS frequency is not determined by the expression level of the target gene, but by the presence of particular gene features facilitating or hindering the trans-splicing mechanism. Our in-depth investigation of SLTS events demonstrates widespread alternative trans-splicing (ATS) acceptor sites occurring in different regions along the entire gene body, highlighting another important role of SLTS generating alternative RNA isoforms in the parasite, besides the polycistron resolution. Particularly for introns where SLTS directly competes for the same acceptor substrate with cis-splicing, we identified for the first time additional and important features that might determine the type of splicing. Our study substantially extends the current knowledge of RNA processing by SLTS in S. mansoni, and provide basis for future studies on the trans-splicing mechanism in other eukaryotes. Nature Publishing Group UK 2018-03-01 /pmc/articles/PMC5832876/ /pubmed/29497070 http://dx.doi.org/10.1038/s41598-018-22093-3 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Boroni, Mariana
Sammeth, Michael
Gava, Sandra Grossi
Jorge, Natasha Andressa Nogueira
Macedo, Andréa Mara
Machado, Carlos Renato
Mourão, Marina Moraes
Franco, Glória Regina
Landscape of the spliced leader trans-splicing mechanism in Schistosoma mansoni
title Landscape of the spliced leader trans-splicing mechanism in Schistosoma mansoni
title_full Landscape of the spliced leader trans-splicing mechanism in Schistosoma mansoni
title_fullStr Landscape of the spliced leader trans-splicing mechanism in Schistosoma mansoni
title_full_unstemmed Landscape of the spliced leader trans-splicing mechanism in Schistosoma mansoni
title_short Landscape of the spliced leader trans-splicing mechanism in Schistosoma mansoni
title_sort landscape of the spliced leader trans-splicing mechanism in schistosoma mansoni
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832876/
https://www.ncbi.nlm.nih.gov/pubmed/29497070
http://dx.doi.org/10.1038/s41598-018-22093-3
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