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Comparative genomics of microsporidian genomes reveals a minimal non-coding RNA set and new insights for transcription in minimal eukaryotic genomes

Microsporidia are ubiquitous intracellular pathogens whose opportunistic nature led to their increased recognition with the rise of the AIDS pandemic. As the RNA world was largely unexplored in this parasitic lineage, we developed a dedicated in silico methodology to carry out exhaustive identificat...

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Autores principales: Belkorchia, Abdel, Pombert, Jean-François, Polonais, Valérie, Parisot, Nicolas, Delbac, Frédéric, Brugère, Jean-François, Peyret, Pierre, Gaspin, Christine, Peyretaillade, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499648/
https://www.ncbi.nlm.nih.gov/pubmed/28338834
http://dx.doi.org/10.1093/dnares/dsx002
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author Belkorchia, Abdel
Pombert, Jean-François
Polonais, Valérie
Parisot, Nicolas
Delbac, Frédéric
Brugère, Jean-François
Peyret, Pierre
Gaspin, Christine
Peyretaillade, Eric
author_facet Belkorchia, Abdel
Pombert, Jean-François
Polonais, Valérie
Parisot, Nicolas
Delbac, Frédéric
Brugère, Jean-François
Peyret, Pierre
Gaspin, Christine
Peyretaillade, Eric
author_sort Belkorchia, Abdel
collection PubMed
description Microsporidia are ubiquitous intracellular pathogens whose opportunistic nature led to their increased recognition with the rise of the AIDS pandemic. As the RNA world was largely unexplored in this parasitic lineage, we developed a dedicated in silico methodology to carry out exhaustive identification of ncRNAs across the Encephalitozoon and Nosema genera. Thus, the previously missing U1 small nuclear RNA (snRNA) and small nucleolar RNAs (snoRNAs) targeting only the LSU rRNA were highlighted and were further validated using 5' and 3'RACE-PCR experiments. Overall, the 15 ncRNAs that were found shared between Encephalitozoon and Nosema spp. may represent the minimal core set required for parasitic life. Interestingly, the systematic presence of a CCC- or GGG-like motif in 5' of all ncRNA and mRNA gene transcripts regardless of the RNA polymerase involved suggests that the RNA polymerase machineries in microsporidia species could use common factors. Our data provide additional insights in accordance with the simplification processes observed in these reduce genomes and underline the usefulness of sequencing closely related species to help identify highly divergent ncRNAs in these parasites.
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spelling pubmed-54996482017-07-10 Comparative genomics of microsporidian genomes reveals a minimal non-coding RNA set and new insights for transcription in minimal eukaryotic genomes Belkorchia, Abdel Pombert, Jean-François Polonais, Valérie Parisot, Nicolas Delbac, Frédéric Brugère, Jean-François Peyret, Pierre Gaspin, Christine Peyretaillade, Eric DNA Res Full Papers Microsporidia are ubiquitous intracellular pathogens whose opportunistic nature led to their increased recognition with the rise of the AIDS pandemic. As the RNA world was largely unexplored in this parasitic lineage, we developed a dedicated in silico methodology to carry out exhaustive identification of ncRNAs across the Encephalitozoon and Nosema genera. Thus, the previously missing U1 small nuclear RNA (snRNA) and small nucleolar RNAs (snoRNAs) targeting only the LSU rRNA were highlighted and were further validated using 5' and 3'RACE-PCR experiments. Overall, the 15 ncRNAs that were found shared between Encephalitozoon and Nosema spp. may represent the minimal core set required for parasitic life. Interestingly, the systematic presence of a CCC- or GGG-like motif in 5' of all ncRNA and mRNA gene transcripts regardless of the RNA polymerase involved suggests that the RNA polymerase machineries in microsporidia species could use common factors. Our data provide additional insights in accordance with the simplification processes observed in these reduce genomes and underline the usefulness of sequencing closely related species to help identify highly divergent ncRNAs in these parasites. Oxford University Press 2017-06 2017-02-28 /pmc/articles/PMC5499648/ /pubmed/28338834 http://dx.doi.org/10.1093/dnares/dsx002 Text en © The Author 2017. Published by Oxford University Press on behalf of Kazusa DNA Research Institute. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Full Papers
Belkorchia, Abdel
Pombert, Jean-François
Polonais, Valérie
Parisot, Nicolas
Delbac, Frédéric
Brugère, Jean-François
Peyret, Pierre
Gaspin, Christine
Peyretaillade, Eric
Comparative genomics of microsporidian genomes reveals a minimal non-coding RNA set and new insights for transcription in minimal eukaryotic genomes
title Comparative genomics of microsporidian genomes reveals a minimal non-coding RNA set and new insights for transcription in minimal eukaryotic genomes
title_full Comparative genomics of microsporidian genomes reveals a minimal non-coding RNA set and new insights for transcription in minimal eukaryotic genomes
title_fullStr Comparative genomics of microsporidian genomes reveals a minimal non-coding RNA set and new insights for transcription in minimal eukaryotic genomes
title_full_unstemmed Comparative genomics of microsporidian genomes reveals a minimal non-coding RNA set and new insights for transcription in minimal eukaryotic genomes
title_short Comparative genomics of microsporidian genomes reveals a minimal non-coding RNA set and new insights for transcription in minimal eukaryotic genomes
title_sort comparative genomics of microsporidian genomes reveals a minimal non-coding rna set and new insights for transcription in minimal eukaryotic genomes
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499648/
https://www.ncbi.nlm.nih.gov/pubmed/28338834
http://dx.doi.org/10.1093/dnares/dsx002
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