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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of Genetic Engineering and Biotechnology 2023-12, Vol.21 (1), p.3-18, Article 3
Hauptverfasser: Bahariah, Bohari, Masani, Mat Yunus Abdul, Fizree, Md Piji Mohd Al Akmarul, Rasid, Omar Abd, Parveez, Ghulam Kadir Ahmad
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 18
container_issue 1
container_start_page 3
container_title Journal of Genetic Engineering and Biotechnology
container_volume 21
creator Bahariah, Bohari
Masani, Mat Yunus Abdul
Fizree, Md Piji Mohd Al Akmarul
Rasid, Omar Abd
Parveez, Ghulam Kadir Ahmad
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
fullrecord <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9834484</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A733018964</galeid><doaj_id>oai_doaj_org_article_5bcf3caaa0f44b778f302d56cafc0492</doaj_id><sourcerecordid>A733018964</sourcerecordid><originalsourceid>FETCH-LOGICAL-c612t-79fc40dd7911d209aa8afc6a33e6a9827308b8f021bd14c93d46b0602d4127c83</originalsourceid><addsrcrecordid>eNp9kk1v1DAQhiMEolXpH-CAInHhktbjr9gXpNW2hZWKqEqRuFmO4wSvEnuxEwT_Hu-mFMoB-2DL884zM9ZbFC8BnQEIfp4oAQoVwrhCiDJZsSfFMUYSVUxi9LQ4Bi7qClj95ag4TWmL8mJUAIPnxRHhnCAE8riwH-ZhcrvB_ijXt5tPN7fna51k2VtvK9u6yfm-3A166kIcS-fL4IZyp4exnHTs7SE8zpOeXPBpH7_sr1YXuNS-zdeb1d2BlF4Uzzo9JHt6f54Un68u79bvq-uP7zbr1XVlOOCpqmVnKGrbWgK0eRathe4M14RYrqXANUGiER3C0LRAjSQt5Q3iCLcUcG0EOSk2C7cNeqt20Y06_lRBO3V4CLFXOk7ODFaxxnTEaK1RR2lT16IjmcO4yRURlTiz3i6s3dyMtjXWT1EPj6CPI959VX34rqQglAqaAW_uATF8m22a1OiSscOgvQ1zUgQYAQ6M7Wu9_ke6DXP0-asUrjlFDAiGrDpbVL3OAzjfhVzX5N3a0Zngbefy-6omBIGQfN8BXhJMDClF2z10D0jtXaQWF6nsInVwkWI56dXfcz-k_PZMFpBFkHLI9zb-afY_2F8MV9B6</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2764051321</pqid></control><display><type>article</type><title>Multiplex CRISPR/Cas9 gene-editing platform in oil palm targeting mutations in EgFAD2 and EgPAT genes</title><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Springer Nature OA Free Journals</source><creator>Bahariah, Bohari ; Masani, Mat Yunus Abdul ; Fizree, Md Piji Mohd Al Akmarul ; Rasid, Omar Abd ; Parveez, Ghulam Kadir Ahmad</creator><creatorcontrib>Bahariah, Bohari ; Masani, Mat Yunus Abdul ; Fizree, Md Piji Mohd Al Akmarul ; Rasid, Omar Abd ; Parveez, Ghulam Kadir Ahmad</creatorcontrib><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><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 &amp; 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 &amp; 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 &amp; 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 &amp; 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>
fulltext fulltext
identifier ISSN: 1687-157X
ispartof Journal of Genetic Engineering and Biotechnology, 2023-12, Vol.21 (1), p.3-18, Article 3
issn 1687-157X
2090-5920
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9834484
source DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Springer Nature OA Free Journals
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T21%3A30%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Multiplex%20CRISPR/Cas9%20gene-editing%20platform%20in%20oil%20palm%20targeting%20mutations%20in%20EgFAD2%20and%20EgPAT%20genes&rft.jtitle=Journal%20of%20Genetic%20Engineering%20and%20Biotechnology&rft.au=Bahariah,%20Bohari&rft.date=2023-12-01&rft.volume=21&rft.issue=1&rft.spage=3&rft.epage=18&rft.pages=3-18&rft.artnum=3&rft.issn=1687-157X&rft.eissn=2090-5920&rft_id=info:doi/10.1186/s43141-022-00459-5&rft_dat=%3Cgale_doaj_%3EA733018964%3C/gale_doaj_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2764051321&rft_id=info:pmid/36630019&rft_galeid=A733018964&rft_doaj_id=oai_doaj_org_article_5bcf3caaa0f44b778f302d56cafc0492&rfr_iscdi=true