Localization of a bacterial group II intron-encoded protein in eukaryotic nuclear splicing-related cell compartments.

Some bacterial group II introns are widely used for genetic engineering in bacteria, because they can be reprogrammed to insert into the desired DNA target sites. There is considerable interest in developing this group II intron gene targeting technology for use in eukaryotes, but nuclear genomes pr...

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Autores principales: Rafael Nisa-Martínez, Philippe Laporte, José Ignacio Jiménez-Zurdo, Florian Frugier, Martin Crespi, Nicolás Toro
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Publicado: Public Library of Science (PLoS) 2013
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spelling oai:doaj.org-article:ab71968e57af4dc7bf054431a3df2b702021-11-18T08:39:26ZLocalization of a bacterial group II intron-encoded protein in eukaryotic nuclear splicing-related cell compartments.1932-620310.1371/journal.pone.0084056https://doaj.org/article/ab71968e57af4dc7bf054431a3df2b702013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24391881/?tool=EBIhttps://doaj.org/toc/1932-6203Some bacterial group II introns are widely used for genetic engineering in bacteria, because they can be reprogrammed to insert into the desired DNA target sites. There is considerable interest in developing this group II intron gene targeting technology for use in eukaryotes, but nuclear genomes present several obstacles to the use of this approach. The nuclear genomes of eukaryotes do not contain group II introns, but these introns are thought to have been the progenitors of nuclear spliceosomal introns. We investigated the expression and subcellular localization of the bacterial RmInt1 group II intron-encoded protein (IEP) in Arabidopsis thaliana protoplasts. Following the expression of translational fusions of the wild-type protein and several mutant variants with EGFP, the full-length IEP was found exclusively in the nucleolus, whereas the maturase domain alone targeted EGFP to nuclear speckles. The distribution of the bacterial RmInt1 IEP in plant cell protoplasts suggests that the compartmentalization of eukaryotic cells into nucleus and cytoplasm does not prevent group II introns from invading the host genome. Furthermore, the trafficking of the IEP between the nucleolus and the speckles upon maturase inactivation is consistent with the hypothesis that the spliceosomal machinery evolved from group II introns.Rafael Nisa-MartínezPhilippe LaporteJosé Ignacio Jiménez-ZurdoFlorian FrugierMartin CrespiNicolás ToroPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 12, p e84056 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Rafael Nisa-Martínez
Philippe Laporte
José Ignacio Jiménez-Zurdo
Florian Frugier
Martin Crespi
Nicolás Toro
Localization of a bacterial group II intron-encoded protein in eukaryotic nuclear splicing-related cell compartments.
description Some bacterial group II introns are widely used for genetic engineering in bacteria, because they can be reprogrammed to insert into the desired DNA target sites. There is considerable interest in developing this group II intron gene targeting technology for use in eukaryotes, but nuclear genomes present several obstacles to the use of this approach. The nuclear genomes of eukaryotes do not contain group II introns, but these introns are thought to have been the progenitors of nuclear spliceosomal introns. We investigated the expression and subcellular localization of the bacterial RmInt1 group II intron-encoded protein (IEP) in Arabidopsis thaliana protoplasts. Following the expression of translational fusions of the wild-type protein and several mutant variants with EGFP, the full-length IEP was found exclusively in the nucleolus, whereas the maturase domain alone targeted EGFP to nuclear speckles. The distribution of the bacterial RmInt1 IEP in plant cell protoplasts suggests that the compartmentalization of eukaryotic cells into nucleus and cytoplasm does not prevent group II introns from invading the host genome. Furthermore, the trafficking of the IEP between the nucleolus and the speckles upon maturase inactivation is consistent with the hypothesis that the spliceosomal machinery evolved from group II introns.
format article
author Rafael Nisa-Martínez
Philippe Laporte
José Ignacio Jiménez-Zurdo
Florian Frugier
Martin Crespi
Nicolás Toro
author_facet Rafael Nisa-Martínez
Philippe Laporte
José Ignacio Jiménez-Zurdo
Florian Frugier
Martin Crespi
Nicolás Toro
author_sort Rafael Nisa-Martínez
title Localization of a bacterial group II intron-encoded protein in eukaryotic nuclear splicing-related cell compartments.
title_short Localization of a bacterial group II intron-encoded protein in eukaryotic nuclear splicing-related cell compartments.
title_full Localization of a bacterial group II intron-encoded protein in eukaryotic nuclear splicing-related cell compartments.
title_fullStr Localization of a bacterial group II intron-encoded protein in eukaryotic nuclear splicing-related cell compartments.
title_full_unstemmed Localization of a bacterial group II intron-encoded protein in eukaryotic nuclear splicing-related cell compartments.
title_sort localization of a bacterial group ii intron-encoded protein in eukaryotic nuclear splicing-related cell compartments.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/ab71968e57af4dc7bf054431a3df2b70
work_keys_str_mv AT rafaelnisamartinez localizationofabacterialgroupiiintronencodedproteinineukaryoticnuclearsplicingrelatedcellcompartments
AT philippelaporte localizationofabacterialgroupiiintronencodedproteinineukaryoticnuclearsplicingrelatedcellcompartments
AT joseignaciojimenezzurdo localizationofabacterialgroupiiintronencodedproteinineukaryoticnuclearsplicingrelatedcellcompartments
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