Development of CRISPR/Cas9 plasmid for multiple sites genome editing in oil palm (Elaeis guineensis Jacq.)
Genome editing technology via CRISPR/Cas9 system is a versatile technique with numerous potential applications, particularly in agriculture. In this study, we attempted to develop a CRISPR/Cas9 plasmid containing four sgRNA to allow multiple gene editing in the oil palm genome. In the first step, we...
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creator | Aprilyanto, Victor Darmawan, Chris Utomo, Condro Liwang, Tony |
description | Genome editing technology via CRISPR/Cas9 system is a versatile technique with numerous potential applications, particularly in agriculture. In this study, we attempted to develop a CRISPR/Cas9 plasmid containing four sgRNA to allow multiple gene editing in the oil palm genome. In the first step, we used an in silico approach to finding the optimum 20-nt guides from four gene regions across oil palm genome. These guides were later joined with a promoter and tracr-RNA fragment to construct a 472 bp module, and together with three tetranucleotide linkers and restriction sites at both terminals gave an insert of length 1 918 bp. This insert was then incorporated into CRISPR/Cas9 vector, and the final plasmid was sequence validated. |
doi_str_mv | 10.1063/1.5098407 |
format | Conference Proceeding |
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In this study, we attempted to develop a CRISPR/Cas9 plasmid containing four sgRNA to allow multiple gene editing in the oil palm genome. In the first step, we used an in silico approach to finding the optimum 20-nt guides from four gene regions across oil palm genome. These guides were later joined with a promoter and tracr-RNA fragment to construct a 472 bp module, and together with three tetranucleotide linkers and restriction sites at both terminals gave an insert of length 1 918 bp. 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In this study, we attempted to develop a CRISPR/Cas9 plasmid containing four sgRNA to allow multiple gene editing in the oil palm genome. In the first step, we used an in silico approach to finding the optimum 20-nt guides from four gene regions across oil palm genome. These guides were later joined with a promoter and tracr-RNA fragment to construct a 472 bp module, and together with three tetranucleotide linkers and restriction sites at both terminals gave an insert of length 1 918 bp. This insert was then incorporated into CRISPR/Cas9 vector, and the final plasmid was sequence validated.</abstract><cop>Melville</cop><pub>American Institute of Physics</pub><doi>10.1063/1.5098407</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Agricultural practices CRISPR Genetic modification Genomes Ribonucleic acid RNA |
title | Development of CRISPR/Cas9 plasmid for multiple sites genome editing in oil palm (Elaeis guineensis Jacq.) |
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