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Bacterial Cellular Engineering by Genome Editing and Gene Silencing

Genome editing is an important technology for bacterial cellular engineering, which is commonly conducted by homologous recombination-based procedures, including gene knockout (disruption), knock-in (insertion), and allelic exchange. In addition, some new recombination-independent approaches have em...

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Detalles Bibliográficos
Autores principales: Nakashima, Nobutaka, Miyazaki, Kentaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3958881/
https://www.ncbi.nlm.nih.gov/pubmed/24552876
http://dx.doi.org/10.3390/ijms15022773
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author Nakashima, Nobutaka
Miyazaki, Kentaro
author_facet Nakashima, Nobutaka
Miyazaki, Kentaro
author_sort Nakashima, Nobutaka
collection PubMed
description Genome editing is an important technology for bacterial cellular engineering, which is commonly conducted by homologous recombination-based procedures, including gene knockout (disruption), knock-in (insertion), and allelic exchange. In addition, some new recombination-independent approaches have emerged that utilize catalytic RNAs, artificial nucleases, nucleic acid analogs, and peptide nucleic acids. Apart from these methods, which directly modify the genomic structure, an alternative approach is to conditionally modify the gene expression profile at the posttranscriptional level without altering the genomes. This is performed by expressing antisense RNAs to knock down (silence) target mRNAs in vivo. This review describes the features and recent advances on methods used in genomic engineering and silencing technologies that are advantageously used for bacterial cellular engineering.
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spelling pubmed-39588812014-03-20 Bacterial Cellular Engineering by Genome Editing and Gene Silencing Nakashima, Nobutaka Miyazaki, Kentaro Int J Mol Sci Review Genome editing is an important technology for bacterial cellular engineering, which is commonly conducted by homologous recombination-based procedures, including gene knockout (disruption), knock-in (insertion), and allelic exchange. In addition, some new recombination-independent approaches have emerged that utilize catalytic RNAs, artificial nucleases, nucleic acid analogs, and peptide nucleic acids. Apart from these methods, which directly modify the genomic structure, an alternative approach is to conditionally modify the gene expression profile at the posttranscriptional level without altering the genomes. This is performed by expressing antisense RNAs to knock down (silence) target mRNAs in vivo. This review describes the features and recent advances on methods used in genomic engineering and silencing technologies that are advantageously used for bacterial cellular engineering. Molecular Diversity Preservation International (MDPI) 2014-02-18 /pmc/articles/PMC3958881/ /pubmed/24552876 http://dx.doi.org/10.3390/ijms15022773 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Nakashima, Nobutaka
Miyazaki, Kentaro
Bacterial Cellular Engineering by Genome Editing and Gene Silencing
title Bacterial Cellular Engineering by Genome Editing and Gene Silencing
title_full Bacterial Cellular Engineering by Genome Editing and Gene Silencing
title_fullStr Bacterial Cellular Engineering by Genome Editing and Gene Silencing
title_full_unstemmed Bacterial Cellular Engineering by Genome Editing and Gene Silencing
title_short Bacterial Cellular Engineering by Genome Editing and Gene Silencing
title_sort bacterial cellular engineering by genome editing and gene silencing
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3958881/
https://www.ncbi.nlm.nih.gov/pubmed/24552876
http://dx.doi.org/10.3390/ijms15022773
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