Recent Advances in CRISPR/Cas9-Mediated Genome Editing in Dictyostelium

In the last 30 years, knockout of target genes via homologous recombination has been widely performed to clarify the physiological functions of proteins in Dictyostelium. As of late, CRISPR/Cas9-mediated genome editing has become a versatile tool in various organisms, including Dictyostelium, enabli...

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Main Authors: Tetsuya Muramoto, Hoshie Iriki, Jun Watanabe, Takefumi Kawata
Format: Article
Language:English
Published: MDPI AG 2019-01-01
Series:Cells
Subjects:
Online Access:http://www.mdpi.com/2073-4409/8/1/46
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spelling doaj-2aaf259b101646c48561331be55ee7d02020-11-25T00:38:32ZengMDPI AGCells2073-44092019-01-01814610.3390/cells8010046cells8010046Recent Advances in CRISPR/Cas9-Mediated Genome Editing in DictyosteliumTetsuya Muramoto0Hoshie Iriki1Jun Watanabe2Takefumi Kawata3Department of Biology, Faculty of Science, Toho University, 2-2-1 Miyama, Funabashi, Chiba 274-8510, JapanDepartment of Biology, Faculty of Science, Toho University, 2-2-1 Miyama, Funabashi, Chiba 274-8510, JapanDepartment of Biology, Faculty of Science, Toho University, 2-2-1 Miyama, Funabashi, Chiba 274-8510, JapanDepartment of Biology, Faculty of Science, Toho University, 2-2-1 Miyama, Funabashi, Chiba 274-8510, JapanIn the last 30 years, knockout of target genes via homologous recombination has been widely performed to clarify the physiological functions of proteins in Dictyostelium. As of late, CRISPR/Cas9-mediated genome editing has become a versatile tool in various organisms, including Dictyostelium, enabling rapid high-fidelity modification of endogenous genes. Here we reviewed recent progress in genome editing in Dictyostelium and summarised useful CRISPR vectors that express sgRNA and Cas9, including several microorganisms. Using these vectors, precise genome modifications can be achieved within 2–3 weeks, beginning with the design of the target sequence. Finally, we discussed future perspectives on the use of CRISPR/Cas9-mediated genome editing in Dictyostelium.http://www.mdpi.com/2073-4409/8/1/46CRISPR/Cas9CRISPR vectorDictyosteliumgenome editingtRNA-based expressionAmoebozoa
collection DOAJ
language English
format Article
sources DOAJ
author Tetsuya Muramoto
Hoshie Iriki
Jun Watanabe
Takefumi Kawata
spellingShingle Tetsuya Muramoto
Hoshie Iriki
Jun Watanabe
Takefumi Kawata
Recent Advances in CRISPR/Cas9-Mediated Genome Editing in Dictyostelium
Cells
CRISPR/Cas9
CRISPR vector
Dictyostelium
genome editing
tRNA-based expression
Amoebozoa
author_facet Tetsuya Muramoto
Hoshie Iriki
Jun Watanabe
Takefumi Kawata
author_sort Tetsuya Muramoto
title Recent Advances in CRISPR/Cas9-Mediated Genome Editing in Dictyostelium
title_short Recent Advances in CRISPR/Cas9-Mediated Genome Editing in Dictyostelium
title_full Recent Advances in CRISPR/Cas9-Mediated Genome Editing in Dictyostelium
title_fullStr Recent Advances in CRISPR/Cas9-Mediated Genome Editing in Dictyostelium
title_full_unstemmed Recent Advances in CRISPR/Cas9-Mediated Genome Editing in Dictyostelium
title_sort recent advances in crispr/cas9-mediated genome editing in dictyostelium
publisher MDPI AG
series Cells
issn 2073-4409
publishDate 2019-01-01
description In the last 30 years, knockout of target genes via homologous recombination has been widely performed to clarify the physiological functions of proteins in Dictyostelium. As of late, CRISPR/Cas9-mediated genome editing has become a versatile tool in various organisms, including Dictyostelium, enabling rapid high-fidelity modification of endogenous genes. Here we reviewed recent progress in genome editing in Dictyostelium and summarised useful CRISPR vectors that express sgRNA and Cas9, including several microorganisms. Using these vectors, precise genome modifications can be achieved within 2–3 weeks, beginning with the design of the target sequence. Finally, we discussed future perspectives on the use of CRISPR/Cas9-mediated genome editing in Dictyostelium.
topic CRISPR/Cas9
CRISPR vector
Dictyostelium
genome editing
tRNA-based expression
Amoebozoa
url http://www.mdpi.com/2073-4409/8/1/46
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