Multiplex CRISPR/Cas9 gene-editing platform in oil palm targeting mutations in EgFAD2 and EgPAT genes
Background CRISPR/Cas9 is the most powerful and versatile genome-editing tool that permits multiplexed-targeted gene modifications for the genetic enhancement of oil palm. Multiplex genome-editing has recently been developed for modifying multiple loci in a gene or multiple genes in a genome with hi...
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description | Background
CRISPR/Cas9 is the most powerful and versatile genome-editing tool that permits multiplexed-targeted gene modifications for the genetic enhancement of oil palm. Multiplex genome-editing has recently been developed for modifying multiple loci in a gene or multiple genes in a genome with high precision. This study focuses on the development of high-oleic oil palm, the primary target trait for healthy low-saturated oil. To achieve this, the
fatty acid desaturase 2
(
FAD2
) and
palmitoyl-acyl carrier protein thioesterase
(
PAT
) genes, both of which are associated with fatty acid metabolism biosynthesis pathways in oil palm, need to be knocked out. The knockout of
FAD2
and
PAT
leads to an accumulation of oleic acid content in oil palms.
Results
A total of four single-guide RNAs (sgRNAs) were designed in silico based on the genomic sequences of
EgFAD2
and
EgPAT.
Using robust plant CRISPR/Cas9 vector technology, multiple sgRNA expression cassettes were efficiently constructed into a single-binary CRISPR/Cas9 vector to edit the
EgFAD2
and
EgPAT
genes. Each of the constructed transformation vectors was then delivered into oil palm embryogenic calli using the biolistic,
Agrobacterium
-mediated, and PEG-mediated protoplast transformation methods. Sequence analysis of PCR products from 15 samples confirmed that mutations were introduced at four target sites of the oil palm
EgFAD2
and
EgPAT
genes. Single- and double-knockout mutants of both genes were generated, with large and small deletions within the targeted regions. Mutations found at EgFAD2 and EgPAT target sites indicate that the Cas9/sgRNA genome-editing system effectively knocked out both genes in oil palm.
Conclusion
This technology is the first in oil palm to use CRISPR/Cas9 genome-editing to target high-oleic-associated genes. These findings showed that multiplex genome-editing in oil palm could be achieved using multiple sgRNAs. Targeted mutations detected establish that the CRISPR/Cas9 technology offers a great potential for oil palm. |
doi_str_mv | 10.1186/s43141-022-00459-5 |
format | Article |
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CRISPR/Cas9 is the most powerful and versatile genome-editing tool that permits multiplexed-targeted gene modifications for the genetic enhancement of oil palm. Multiplex genome-editing has recently been developed for modifying multiple loci in a gene or multiple genes in a genome with high precision. This study focuses on the development of high-oleic oil palm, the primary target trait for healthy low-saturated oil. To achieve this, the
fatty acid desaturase 2
(
FAD2
) and
palmitoyl-acyl carrier protein thioesterase
(
PAT
) genes, both of which are associated with fatty acid metabolism biosynthesis pathways in oil palm, need to be knocked out. The knockout of
FAD2
and
PAT
leads to an accumulation of oleic acid content in oil palms.
Results
A total of four single-guide RNAs (sgRNAs) were designed in silico based on the genomic sequences of
EgFAD2
and
EgPAT.
Using robust plant CRISPR/Cas9 vector technology, multiple sgRNA expression cassettes were efficiently constructed into a single-binary CRISPR/Cas9 vector to edit the
EgFAD2
and
EgPAT
genes. Each of the constructed transformation vectors was then delivered into oil palm embryogenic calli using the biolistic,
Agrobacterium
-mediated, and PEG-mediated protoplast transformation methods. Sequence analysis of PCR products from 15 samples confirmed that mutations were introduced at four target sites of the oil palm
EgFAD2
and
EgPAT
genes. Single- and double-knockout mutants of both genes were generated, with large and small deletions within the targeted regions. Mutations found at EgFAD2 and EgPAT target sites indicate that the Cas9/sgRNA genome-editing system effectively knocked out both genes in oil palm.
Conclusion
This technology is the first in oil palm to use CRISPR/Cas9 genome-editing to target high-oleic-associated genes. These findings showed that multiplex genome-editing in oil palm could be achieved using multiple sgRNAs. Targeted mutations detected establish that the CRISPR/Cas9 technology offers a great potential for oil palm.</description><identifier>ISSN: 1687-157X</identifier><identifier>EISSN: 2090-5920</identifier><identifier>DOI: 10.1186/s43141-022-00459-5</identifier><identifier>PMID: 36630019</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Acyl carrier protein ; biolistics ; Biomedical Engineering and Bioengineering ; Biosynthesis ; biotechnology ; callus ; computer simulation ; CRISPR ; CRISPR-Cas systems ; CRISPR/Cas9 ; Desaturase ; Editing ; EgFAD2 ; EgPAT ; Elaeis guineensis ; Engineering ; Enzymes ; Expression vectors ; fatty acid desaturase ; fatty acid metabolism ; Fatty acids ; gene editing ; Genes ; Genetic aspects ; Genetic engineering ; genetic improvement ; Genetic modification ; Genetic research ; Genetic transformation ; Genetically modified organisms ; Genome editing ; Genomes ; Genomics ; Monounsaturated fatty acids ; Multiplexing ; Mutation ; Oil palm ; oils ; Oils & fats ; Oleic acid ; protoplasts ; RNA polymerase ; Sequence analysis ; Vegetable oils</subject><ispartof>Journal of Genetic Engineering and Biotechnology, 2023-12, Vol.21 (1), p.3-18, Article 3</ispartof><rights>The Author(s) 2023</rights><rights>2023. The Author(s).</rights><rights>COPYRIGHT 2023 Springer</rights><rights>The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c612t-79fc40dd7911d209aa8afc6a33e6a9827308b8f021bd14c93d46b0602d4127c83</citedby><cites>FETCH-LOGICAL-c612t-79fc40dd7911d209aa8afc6a33e6a9827308b8f021bd14c93d46b0602d4127c83</cites><orcidid>0000-0003-0704-2900 ; 0000-0003-3721-4734</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834484/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834484/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36630019$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bahariah, Bohari</creatorcontrib><creatorcontrib>Masani, Mat Yunus Abdul</creatorcontrib><creatorcontrib>Fizree, Md Piji Mohd Al Akmarul</creatorcontrib><creatorcontrib>Rasid, Omar Abd</creatorcontrib><creatorcontrib>Parveez, Ghulam Kadir Ahmad</creatorcontrib><title>Multiplex CRISPR/Cas9 gene-editing platform in oil palm targeting mutations in EgFAD2 and EgPAT genes</title><title>Journal of Genetic Engineering and Biotechnology</title><addtitle>J Genet Eng Biotechnol</addtitle><addtitle>J Genet Eng Biotechnol</addtitle><description>Background
CRISPR/Cas9 is the most powerful and versatile genome-editing tool that permits multiplexed-targeted gene modifications for the genetic enhancement of oil palm. Multiplex genome-editing has recently been developed for modifying multiple loci in a gene or multiple genes in a genome with high precision. This study focuses on the development of high-oleic oil palm, the primary target trait for healthy low-saturated oil. To achieve this, the
fatty acid desaturase 2
(
FAD2
) and
palmitoyl-acyl carrier protein thioesterase
(
PAT
) genes, both of which are associated with fatty acid metabolism biosynthesis pathways in oil palm, need to be knocked out. The knockout of
FAD2
and
PAT
leads to an accumulation of oleic acid content in oil palms.
Results
A total of four single-guide RNAs (sgRNAs) were designed in silico based on the genomic sequences of
EgFAD2
and
EgPAT.
Using robust plant CRISPR/Cas9 vector technology, multiple sgRNA expression cassettes were efficiently constructed into a single-binary CRISPR/Cas9 vector to edit the
EgFAD2
and
EgPAT
genes. Each of the constructed transformation vectors was then delivered into oil palm embryogenic calli using the biolistic,
Agrobacterium
-mediated, and PEG-mediated protoplast transformation methods. Sequence analysis of PCR products from 15 samples confirmed that mutations were introduced at four target sites of the oil palm
EgFAD2
and
EgPAT
genes. Single- and double-knockout mutants of both genes were generated, with large and small deletions within the targeted regions. Mutations found at EgFAD2 and EgPAT target sites indicate that the Cas9/sgRNA genome-editing system effectively knocked out both genes in oil palm.
Conclusion
This technology is the first in oil palm to use CRISPR/Cas9 genome-editing to target high-oleic-associated genes. These findings showed that multiplex genome-editing in oil palm could be achieved using multiple sgRNAs. Targeted mutations detected establish that the CRISPR/Cas9 technology offers a great potential for oil palm.</description><subject>Acyl carrier protein</subject><subject>biolistics</subject><subject>Biomedical Engineering and Bioengineering</subject><subject>Biosynthesis</subject><subject>biotechnology</subject><subject>callus</subject><subject>computer simulation</subject><subject>CRISPR</subject><subject>CRISPR-Cas systems</subject><subject>CRISPR/Cas9</subject><subject>Desaturase</subject><subject>Editing</subject><subject>EgFAD2</subject><subject>EgPAT</subject><subject>Elaeis guineensis</subject><subject>Engineering</subject><subject>Enzymes</subject><subject>Expression vectors</subject><subject>fatty acid desaturase</subject><subject>fatty acid metabolism</subject><subject>Fatty acids</subject><subject>gene editing</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genetic engineering</subject><subject>genetic improvement</subject><subject>Genetic modification</subject><subject>Genetic research</subject><subject>Genetic transformation</subject><subject>Genetically modified organisms</subject><subject>Genome editing</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Monounsaturated fatty acids</subject><subject>Multiplexing</subject><subject>Mutation</subject><subject>Oil palm</subject><subject>oils</subject><subject>Oils & fats</subject><subject>Oleic acid</subject><subject>protoplasts</subject><subject>RNA polymerase</subject><subject>Sequence analysis</subject><subject>Vegetable oils</subject><issn>1687-157X</issn><issn>2090-5920</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNp9kk1v1DAQhiMEolXpH-CAInHhktbjr9gXpNW2hZWKqEqRuFmO4wSvEnuxEwT_Hu-mFMoB-2DL884zM9ZbFC8BnQEIfp4oAQoVwrhCiDJZsSfFMUYSVUxi9LQ4Bi7qClj95ag4TWmL8mJUAIPnxRHhnCAE8riwH-ZhcrvB_ijXt5tPN7fna51k2VtvK9u6yfm-3A166kIcS-fL4IZyp4exnHTs7SE8zpOeXPBpH7_sr1YXuNS-zdeb1d2BlF4Uzzo9JHt6f54Un68u79bvq-uP7zbr1XVlOOCpqmVnKGrbWgK0eRathe4M14RYrqXANUGiER3C0LRAjSQt5Q3iCLcUcG0EOSk2C7cNeqt20Y06_lRBO3V4CLFXOk7ODFaxxnTEaK1RR2lT16IjmcO4yRURlTiz3i6s3dyMtjXWT1EPj6CPI959VX34rqQglAqaAW_uATF8m22a1OiSscOgvQ1zUgQYAQ6M7Wu9_ke6DXP0-asUrjlFDAiGrDpbVL3OAzjfhVzX5N3a0Zngbefy-6omBIGQfN8BXhJMDClF2z10D0jtXaQWF6nsInVwkWI56dXfcz-k_PZMFpBFkHLI9zb-afY_2F8MV9B6</recordid><startdate>20231201</startdate><enddate>20231201</enddate><creator>Bahariah, Bohari</creator><creator>Masani, Mat Yunus Abdul</creator><creator>Fizree, Md Piji Mohd Al Akmarul</creator><creator>Rasid, Omar Abd</creator><creator>Parveez, Ghulam Kadir Ahmad</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature B.V</general><general>Elsevier</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>L6V</scope><scope>LK8</scope><scope>M7P</scope><scope>M7S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-0704-2900</orcidid><orcidid>https://orcid.org/0000-0003-3721-4734</orcidid></search><sort><creationdate>20231201</creationdate><title>Multiplex CRISPR/Cas9 gene-editing platform in oil palm targeting mutations in EgFAD2 and EgPAT genes</title><author>Bahariah, Bohari ; Masani, Mat Yunus Abdul ; Fizree, Md Piji Mohd Al Akmarul ; Rasid, Omar Abd ; Parveez, Ghulam Kadir Ahmad</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c612t-79fc40dd7911d209aa8afc6a33e6a9827308b8f021bd14c93d46b0602d4127c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Acyl carrier protein</topic><topic>biolistics</topic><topic>Biomedical Engineering and Bioengineering</topic><topic>Biosynthesis</topic><topic>biotechnology</topic><topic>callus</topic><topic>computer simulation</topic><topic>CRISPR</topic><topic>CRISPR-Cas systems</topic><topic>CRISPR/Cas9</topic><topic>Desaturase</topic><topic>Editing</topic><topic>EgFAD2</topic><topic>EgPAT</topic><topic>Elaeis guineensis</topic><topic>Engineering</topic><topic>Enzymes</topic><topic>Expression vectors</topic><topic>fatty acid desaturase</topic><topic>fatty acid metabolism</topic><topic>Fatty acids</topic><topic>gene editing</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genetic engineering</topic><topic>genetic improvement</topic><topic>Genetic modification</topic><topic>Genetic research</topic><topic>Genetic transformation</topic><topic>Genetically modified organisms</topic><topic>Genome editing</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Monounsaturated fatty acids</topic><topic>Multiplexing</topic><topic>Mutation</topic><topic>Oil palm</topic><topic>oils</topic><topic>Oils & fats</topic><topic>Oleic acid</topic><topic>protoplasts</topic><topic>RNA polymerase</topic><topic>Sequence analysis</topic><topic>Vegetable oils</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bahariah, Bohari</creatorcontrib><creatorcontrib>Masani, Mat Yunus Abdul</creatorcontrib><creatorcontrib>Fizree, Md Piji Mohd Al Akmarul</creatorcontrib><creatorcontrib>Rasid, Omar Abd</creatorcontrib><creatorcontrib>Parveez, Ghulam Kadir Ahmad</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of Genetic Engineering and Biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bahariah, Bohari</au><au>Masani, Mat Yunus Abdul</au><au>Fizree, Md Piji Mohd Al Akmarul</au><au>Rasid, Omar Abd</au><au>Parveez, Ghulam Kadir Ahmad</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multiplex CRISPR/Cas9 gene-editing platform in oil palm targeting mutations in EgFAD2 and EgPAT genes</atitle><jtitle>Journal of Genetic Engineering and Biotechnology</jtitle><stitle>J Genet Eng Biotechnol</stitle><addtitle>J Genet Eng Biotechnol</addtitle><date>2023-12-01</date><risdate>2023</risdate><volume>21</volume><issue>1</issue><spage>3</spage><epage>18</epage><pages>3-18</pages><artnum>3</artnum><issn>1687-157X</issn><eissn>2090-5920</eissn><abstract>Background
CRISPR/Cas9 is the most powerful and versatile genome-editing tool that permits multiplexed-targeted gene modifications for the genetic enhancement of oil palm. Multiplex genome-editing has recently been developed for modifying multiple loci in a gene or multiple genes in a genome with high precision. This study focuses on the development of high-oleic oil palm, the primary target trait for healthy low-saturated oil. To achieve this, the
fatty acid desaturase 2
(
FAD2
) and
palmitoyl-acyl carrier protein thioesterase
(
PAT
) genes, both of which are associated with fatty acid metabolism biosynthesis pathways in oil palm, need to be knocked out. The knockout of
FAD2
and
PAT
leads to an accumulation of oleic acid content in oil palms.
Results
A total of four single-guide RNAs (sgRNAs) were designed in silico based on the genomic sequences of
EgFAD2
and
EgPAT.
Using robust plant CRISPR/Cas9 vector technology, multiple sgRNA expression cassettes were efficiently constructed into a single-binary CRISPR/Cas9 vector to edit the
EgFAD2
and
EgPAT
genes. Each of the constructed transformation vectors was then delivered into oil palm embryogenic calli using the biolistic,
Agrobacterium
-mediated, and PEG-mediated protoplast transformation methods. Sequence analysis of PCR products from 15 samples confirmed that mutations were introduced at four target sites of the oil palm
EgFAD2
and
EgPAT
genes. Single- and double-knockout mutants of both genes were generated, with large and small deletions within the targeted regions. Mutations found at EgFAD2 and EgPAT target sites indicate that the Cas9/sgRNA genome-editing system effectively knocked out both genes in oil palm.
Conclusion
This technology is the first in oil palm to use CRISPR/Cas9 genome-editing to target high-oleic-associated genes. These findings showed that multiplex genome-editing in oil palm could be achieved using multiple sgRNAs. Targeted mutations detected establish that the CRISPR/Cas9 technology offers a great potential for oil palm.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>36630019</pmid><doi>10.1186/s43141-022-00459-5</doi><tpages>18</tpages><orcidid>https://orcid.org/0000-0003-0704-2900</orcidid><orcidid>https://orcid.org/0000-0003-3721-4734</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acyl carrier protein biolistics Biomedical Engineering and Bioengineering Biosynthesis biotechnology callus computer simulation CRISPR CRISPR-Cas systems CRISPR/Cas9 Desaturase Editing EgFAD2 EgPAT Elaeis guineensis Engineering Enzymes Expression vectors fatty acid desaturase fatty acid metabolism Fatty acids gene editing Genes Genetic aspects Genetic engineering genetic improvement Genetic modification Genetic research Genetic transformation Genetically modified organisms Genome editing Genomes Genomics Monounsaturated fatty acids Multiplexing Mutation Oil palm oils Oils & fats Oleic acid protoplasts RNA polymerase Sequence analysis Vegetable oils |
title | Multiplex CRISPR/Cas9 gene-editing platform in oil palm targeting mutations in EgFAD2 and EgPAT genes |
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