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Group II intron as cold sensor for self-preservation and bacterial conjugation
Group II introns are self-splicing ribozymes and mobile genetic elements. Splicing is required for both expression of the interrupted host gene and intron retromobility. For the pRS01 plasmid-encoded Lactococcus lactis group II intron, Ll.LtrB, splicing enables expression of the intron's host r...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293003/ https://www.ncbi.nlm.nih.gov/pubmed/32379323 http://dx.doi.org/10.1093/nar/gkaa313 |
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author | Dong, Xiaolong Qu, Guosheng Piazza, Carol Lyn Belfort, Marlene |
author_facet | Dong, Xiaolong Qu, Guosheng Piazza, Carol Lyn Belfort, Marlene |
author_sort | Dong, Xiaolong |
collection | PubMed |
description | Group II introns are self-splicing ribozymes and mobile genetic elements. Splicing is required for both expression of the interrupted host gene and intron retromobility. For the pRS01 plasmid-encoded Lactococcus lactis group II intron, Ll.LtrB, splicing enables expression of the intron's host relaxase protein. Relaxase, in turn, initiates horizontal transfer of the conjugative pRS01 plasmid and stimulates retrotransposition of the intron. Little is known about how splicing of bacterial group II introns is influenced by environmental conditions. Here, we show that low temperatures can inhibit Ll.LtrB intron splicing. Whereas autocatalysis is abolished in the cold, splicing is partially restored by the intron-encoded protein (IEP). Structure profiling reveals cold-induced disruptions of key tertiary interactions, suggesting that a kinetic trap prevents the intron RNA from assuming its native state. Interestingly, while reduced levels of transcription and splicing lead to a paucity of excised intron in the cold, levels of relaxase mRNA are maintained, partially due to diminished intron-mediated mRNA targeting, allowing intron spread by conjugal transfer. Taken together, this study demonstrates not only the intrinsic cold sensitivity of group II intron splicing and the role of the IEP for cold-stress adaptation, but also maintenance of horizontal plasmid and intron transfer under cold-shock. |
format | Online Article Text |
id | pubmed-7293003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-72930032020-06-17 Group II intron as cold sensor for self-preservation and bacterial conjugation Dong, Xiaolong Qu, Guosheng Piazza, Carol Lyn Belfort, Marlene Nucleic Acids Res RNA and RNA-protein complexes Group II introns are self-splicing ribozymes and mobile genetic elements. Splicing is required for both expression of the interrupted host gene and intron retromobility. For the pRS01 plasmid-encoded Lactococcus lactis group II intron, Ll.LtrB, splicing enables expression of the intron's host relaxase protein. Relaxase, in turn, initiates horizontal transfer of the conjugative pRS01 plasmid and stimulates retrotransposition of the intron. Little is known about how splicing of bacterial group II introns is influenced by environmental conditions. Here, we show that low temperatures can inhibit Ll.LtrB intron splicing. Whereas autocatalysis is abolished in the cold, splicing is partially restored by the intron-encoded protein (IEP). Structure profiling reveals cold-induced disruptions of key tertiary interactions, suggesting that a kinetic trap prevents the intron RNA from assuming its native state. Interestingly, while reduced levels of transcription and splicing lead to a paucity of excised intron in the cold, levels of relaxase mRNA are maintained, partially due to diminished intron-mediated mRNA targeting, allowing intron spread by conjugal transfer. Taken together, this study demonstrates not only the intrinsic cold sensitivity of group II intron splicing and the role of the IEP for cold-stress adaptation, but also maintenance of horizontal plasmid and intron transfer under cold-shock. Oxford University Press 2020-06-19 2020-05-07 /pmc/articles/PMC7293003/ /pubmed/32379323 http://dx.doi.org/10.1093/nar/gkaa313 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 | RNA and RNA-protein complexes Dong, Xiaolong Qu, Guosheng Piazza, Carol Lyn Belfort, Marlene Group II intron as cold sensor for self-preservation and bacterial conjugation |
title | Group II intron as cold sensor for self-preservation and bacterial conjugation |
title_full | Group II intron as cold sensor for self-preservation and bacterial conjugation |
title_fullStr | Group II intron as cold sensor for self-preservation and bacterial conjugation |
title_full_unstemmed | Group II intron as cold sensor for self-preservation and bacterial conjugation |
title_short | Group II intron as cold sensor for self-preservation and bacterial conjugation |
title_sort | group ii intron as cold sensor for self-preservation and bacterial conjugation |
topic | RNA and RNA-protein complexes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293003/ https://www.ncbi.nlm.nih.gov/pubmed/32379323 http://dx.doi.org/10.1093/nar/gkaa313 |
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