{"title":"CRISPR/Cas9介导的南瓜植物烯去饱和酶基因编辑","authors":"Shallu Thakur, Geoffrey Meru","doi":"10.1007/s13562-023-00866-w","DOIUrl":null,"url":null,"abstract":"<p>Gene editing using the Clustered Regularly Interspaced Short Palindromic Repeats/CRISPR-associated 9 (CRISPR/Cas9) system has become an important biotechnological tool for studying gene function and improving crops. In the present study, the potential of the system was assessed for squash (<i>Cucurbita pepo</i> subspecies <i>pepo</i>) by targeting phytoene desaturase (<i>PDS</i>) gene using the particle bombardment method. The recombinant pHSE401 vector, carrying two sgRNAs (<i>gRNA1</i> and <i>gRNA2</i>) specific to the <i>PDS</i> homolog (<i>Cp4.1LG08g06310, CpPDS</i>) under the control of <i>Arabidopsis</i> U6 promoter and the Cas9 protein was developed and bombarded into cotyledonary node explants of squash cv. Black Beauty. The transformation efficiency of 4.5% was observed and all the transformants exhibited albino/bleached phenotype. The <i>CpPDS</i> knockout system generated easily detectable bleached/albino explants within 6–8 weeks. The albino phenotype was confirmed through Sanger sequencing which detected several deletion mutations (single, two and three bp deletion) within the <i>CpPDS-gRNA1</i> target. However, no mutations were found within the <i>CpPDS-gRNA2</i> target. This study demonstrated CRISPR/Cas9 as a viable tool for gene editing in squash and provides a platform for the modification of economically important traits in the crop.</p>","PeriodicalId":16835,"journal":{"name":"Journal of Plant Biochemistry and Biotechnology","volume":"58 1","pages":""},"PeriodicalIF":1.6000,"publicationDate":"2023-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"CRISPR/Cas9 mediated editing of phytoene desaturase gene in squash\",\"authors\":\"Shallu Thakur, Geoffrey Meru\",\"doi\":\"10.1007/s13562-023-00866-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Gene editing using the Clustered Regularly Interspaced Short Palindromic Repeats/CRISPR-associated 9 (CRISPR/Cas9) system has become an important biotechnological tool for studying gene function and improving crops. In the present study, the potential of the system was assessed for squash (<i>Cucurbita pepo</i> subspecies <i>pepo</i>) by targeting phytoene desaturase (<i>PDS</i>) gene using the particle bombardment method. The recombinant pHSE401 vector, carrying two sgRNAs (<i>gRNA1</i> and <i>gRNA2</i>) specific to the <i>PDS</i> homolog (<i>Cp4.1LG08g06310, CpPDS</i>) under the control of <i>Arabidopsis</i> U6 promoter and the Cas9 protein was developed and bombarded into cotyledonary node explants of squash cv. Black Beauty. The transformation efficiency of 4.5% was observed and all the transformants exhibited albino/bleached phenotype. The <i>CpPDS</i> knockout system generated easily detectable bleached/albino explants within 6–8 weeks. The albino phenotype was confirmed through Sanger sequencing which detected several deletion mutations (single, two and three bp deletion) within the <i>CpPDS-gRNA1</i> target. However, no mutations were found within the <i>CpPDS-gRNA2</i> target. This study demonstrated CRISPR/Cas9 as a viable tool for gene editing in squash and provides a platform for the modification of economically important traits in the crop.</p>\",\"PeriodicalId\":16835,\"journal\":{\"name\":\"Journal of Plant Biochemistry and Biotechnology\",\"volume\":\"58 1\",\"pages\":\"\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2023-11-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Plant Biochemistry and Biotechnology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s13562-023-00866-w\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Plant Biochemistry and Biotechnology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s13562-023-00866-w","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
CRISPR/Cas9 mediated editing of phytoene desaturase gene in squash
Gene editing using the Clustered Regularly Interspaced Short Palindromic Repeats/CRISPR-associated 9 (CRISPR/Cas9) system has become an important biotechnological tool for studying gene function and improving crops. In the present study, the potential of the system was assessed for squash (Cucurbita pepo subspecies pepo) by targeting phytoene desaturase (PDS) gene using the particle bombardment method. The recombinant pHSE401 vector, carrying two sgRNAs (gRNA1 and gRNA2) specific to the PDS homolog (Cp4.1LG08g06310, CpPDS) under the control of Arabidopsis U6 promoter and the Cas9 protein was developed and bombarded into cotyledonary node explants of squash cv. Black Beauty. The transformation efficiency of 4.5% was observed and all the transformants exhibited albino/bleached phenotype. The CpPDS knockout system generated easily detectable bleached/albino explants within 6–8 weeks. The albino phenotype was confirmed through Sanger sequencing which detected several deletion mutations (single, two and three bp deletion) within the CpPDS-gRNA1 target. However, no mutations were found within the CpPDS-gRNA2 target. This study demonstrated CRISPR/Cas9 as a viable tool for gene editing in squash and provides a platform for the modification of economically important traits in the crop.
期刊介绍:
The Journal publishes review articles, research papers, short communications and commentaries in the areas of plant biochemistry, plant molecular biology, microbial and molecular genetics, DNA finger printing, micropropagation, and plant biotechnology including plant genetic engineering, new molecular tools and techniques, genomics & bioinformatics.