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Group II Intron-Anchored Gene Deletion in Clostridium

Clostridium plays an important role in commercial and medical use, for which targeted gene deletion is difficult. We proposed an intron-anchored gene deletion approach for Clostridium, which combines the advantage of the group II intron “ClosTron” system and homologous recombination. In this approac...

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Detalles Bibliográficos
Autores principales: Jia, Kaizhi, Zhu, Yan, Zhang, Yanping, Li, Yin
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3031624/
https://www.ncbi.nlm.nih.gov/pubmed/21304965
http://dx.doi.org/10.1371/journal.pone.0016693
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author Jia, Kaizhi
Zhu, Yan
Zhang, Yanping
Li, Yin
author_facet Jia, Kaizhi
Zhu, Yan
Zhang, Yanping
Li, Yin
author_sort Jia, Kaizhi
collection PubMed
description Clostridium plays an important role in commercial and medical use, for which targeted gene deletion is difficult. We proposed an intron-anchored gene deletion approach for Clostridium, which combines the advantage of the group II intron “ClosTron” system and homologous recombination. In this approach, an intron carrying a fragment homologous to upstream or downstream of the target site was first inserted into the genome by retrotransposition, followed by homologous recombination, resulting in gene deletion. A functional unknown operon CAC1493–1494 located in the chromosome, and an operon ctfAB located in the megaplasmid of C. acetobutylicum DSM1731 were successfully deleted by using this approach, without leaving antibiotic marker in the genome. We therefore propose this approach can be used for targeted gene deletion in Clostridium. This approach might also be applicable for gene deletion in other bacterial species if group II intron retrotransposition system is established.
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spelling pubmed-30316242011-02-08 Group II Intron-Anchored Gene Deletion in Clostridium Jia, Kaizhi Zhu, Yan Zhang, Yanping Li, Yin PLoS One Research Article Clostridium plays an important role in commercial and medical use, for which targeted gene deletion is difficult. We proposed an intron-anchored gene deletion approach for Clostridium, which combines the advantage of the group II intron “ClosTron” system and homologous recombination. In this approach, an intron carrying a fragment homologous to upstream or downstream of the target site was first inserted into the genome by retrotransposition, followed by homologous recombination, resulting in gene deletion. A functional unknown operon CAC1493–1494 located in the chromosome, and an operon ctfAB located in the megaplasmid of C. acetobutylicum DSM1731 were successfully deleted by using this approach, without leaving antibiotic marker in the genome. We therefore propose this approach can be used for targeted gene deletion in Clostridium. This approach might also be applicable for gene deletion in other bacterial species if group II intron retrotransposition system is established. Public Library of Science 2011-01-31 /pmc/articles/PMC3031624/ /pubmed/21304965 http://dx.doi.org/10.1371/journal.pone.0016693 Text en Jia et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Jia, Kaizhi
Zhu, Yan
Zhang, Yanping
Li, Yin
Group II Intron-Anchored Gene Deletion in Clostridium
title Group II Intron-Anchored Gene Deletion in Clostridium
title_full Group II Intron-Anchored Gene Deletion in Clostridium
title_fullStr Group II Intron-Anchored Gene Deletion in Clostridium
title_full_unstemmed Group II Intron-Anchored Gene Deletion in Clostridium
title_short Group II Intron-Anchored Gene Deletion in Clostridium
title_sort group ii intron-anchored gene deletion in clostridium
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3031624/
https://www.ncbi.nlm.nih.gov/pubmed/21304965
http://dx.doi.org/10.1371/journal.pone.0016693
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