Bxb1 phage recombinase assists genome engineering in Drosophila melanogaster

Rapid and reliable genome modifications provide the basis for detailed in vivo functional analysis of any genomic entity (gene, regulatory DNA, non-coding RNA, etc). With the advent of CRISPR/Cas9 genome editing technology, manipulation of a particular genomic locus has become a routine undertaking...

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Main Authors: Roumen Voutev, Richard S. Mann
Format: Article
Language:English
Published: Taylor & Francis Group 2017-01-01
Series:BioTechniques
Subjects:
Online Access:https://www.future-science.com/doi/10.2144/000114494
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author Roumen Voutev
Richard S. Mann
author_facet Roumen Voutev
Richard S. Mann
author_sort Roumen Voutev
collection DOAJ
description Rapid and reliable genome modifications provide the basis for detailed in vivo functional analysis of any genomic entity (gene, regulatory DNA, non-coding RNA, etc). With the advent of CRISPR/Cas9 genome editing technology, manipulation of a particular genomic locus has become a routine undertaking in variety of model organisms, including the fruit fly Drosophila melanogaster. To further diversify the available tools for genome engineering, we successfully harnessed the phage recombinase Bxb1 to perform recombinase-mediated cassette exchange (RMCE) in D. melanogaster. We demonstrate that Bxb1 possesses highly efficient recombinase activity and could be used alone or in conjunction with other currently available recombinases for creating platforms for cassette exchange of targeted loci.
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spelling doaj-art-96d55635dd7b4ae2b23bf0f0ae7701a42025-08-20T02:25:58ZengTaylor & Francis GroupBioTechniques0736-62051940-98182017-01-01621373810.2144/000114494Bxb1 phage recombinase assists genome engineering in Drosophila melanogasterRoumen Voutev0Richard S. Mann11Departments of Biochemistry and Molecular Biophysics and Systems Biology, Columbia University, New York, NY1Departments of Biochemistry and Molecular Biophysics and Systems Biology, Columbia University, New York, NYRapid and reliable genome modifications provide the basis for detailed in vivo functional analysis of any genomic entity (gene, regulatory DNA, non-coding RNA, etc). With the advent of CRISPR/Cas9 genome editing technology, manipulation of a particular genomic locus has become a routine undertaking in variety of model organisms, including the fruit fly Drosophila melanogaster. To further diversify the available tools for genome engineering, we successfully harnessed the phage recombinase Bxb1 to perform recombinase-mediated cassette exchange (RMCE) in D. melanogaster. We demonstrate that Bxb1 possesses highly efficient recombinase activity and could be used alone or in conjunction with other currently available recombinases for creating platforms for cassette exchange of targeted loci.https://www.future-science.com/doi/10.2144/000114494Bxb1 recombinasecassette exchangegenome editingDrosophila melanogaster
spellingShingle Roumen Voutev
Richard S. Mann
Bxb1 phage recombinase assists genome engineering in Drosophila melanogaster
BioTechniques
Bxb1 recombinase
cassette exchange
genome editing
Drosophila melanogaster
title Bxb1 phage recombinase assists genome engineering in Drosophila melanogaster
title_full Bxb1 phage recombinase assists genome engineering in Drosophila melanogaster
title_fullStr Bxb1 phage recombinase assists genome engineering in Drosophila melanogaster
title_full_unstemmed Bxb1 phage recombinase assists genome engineering in Drosophila melanogaster
title_short Bxb1 phage recombinase assists genome engineering in Drosophila melanogaster
title_sort bxb1 phage recombinase assists genome engineering in drosophila melanogaster
topic Bxb1 recombinase
cassette exchange
genome editing
Drosophila melanogaster
url https://www.future-science.com/doi/10.2144/000114494
work_keys_str_mv AT roumenvoutev bxb1phagerecombinaseassistsgenomeengineeringindrosophilamelanogaster
AT richardsmann bxb1phagerecombinaseassistsgenomeengineeringindrosophilamelanogaster