• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
CRISPR/Cas9-mediated editing of phytoene desaturase () gene in an important staple crop, potato.CRISPR/Cas9介导的重要主粮作物马铃薯中八氢番茄红素去饱和酶()基因的编辑。
3 Biotech. 2023 May;13(5):129. doi: 10.1007/s13205-023-03543-w. Epub 2023 Apr 12.
2
An efficient and specific CRISPR-Cas9 genome editing system targeting soybean phytoene desaturase genes.一种针对大豆八氢番茄红素脱氢酶基因的高效、特异的 CRISPR-Cas9 基因组编辑系统。
BMC Biotechnol. 2022 Feb 15;22(1):7. doi: 10.1186/s12896-022-00737-7.
3
Knockout of phytoene desaturase gene using CRISPR/Cas9 in highbush blueberry.利用CRISPR/Cas9敲除高丛蓝莓中的八氢番茄红素去饱和酶基因。
Front Plant Sci. 2022 Dec 15;13:1074541. doi: 10.3389/fpls.2022.1074541. eCollection 2022.
4
Efficient CRISPR/Cas9 Genome Editing of in Cassava.木薯中高效的CRISPR/Cas9基因组编辑
Front Plant Sci. 2017 Oct 18;8:1780. doi: 10.3389/fpls.2017.01780. eCollection 2017.
5
Generation of transgene-free PDS mutants in potato by Agrobacterium-mediated transformation.利用农杆菌介导转化技术生成无转基因的马铃薯 PDS 突变体。
BMC Biotechnol. 2020 May 12;20(1):25. doi: 10.1186/s12896-020-00621-2.
6
Efficient knockout of phytoene desaturase gene using CRISPR/Cas9 in melon.利用 CRISPR/Cas9 在甜瓜中高效敲除八氢番茄红素脱氢酶基因。
Sci Rep. 2019 Nov 19;9(1):17077. doi: 10.1038/s41598-019-53710-4.
7
Efficient CRISPR/Cas9 genome editing with Citrus embryogenic cell cultures.利用柑橘胚性细胞培养物实现高效的 CRISPR/Cas9 基因组编辑。
BMC Biotechnol. 2020 Nov 10;20(1):58. doi: 10.1186/s12896-020-00652-9.
8
CRISPR/Cas9-mediated efficient editing in phytoene desaturase (PDS) demonstrates precise manipulation in banana cv. Rasthali genome.CRISPR/Cas9介导的八氢番茄红素去饱和酶(PDS)高效编辑证明了对香蕉品种Rasthali基因组的精确操控。
Funct Integr Genomics. 2018 Jan;18(1):89-99. doi: 10.1007/s10142-017-0577-5. Epub 2017 Nov 29.
9
CRISPR/Cas9-mediated editing of gene in onion ( L.).CRISPR/Cas9介导的洋葱(L.)基因编辑。
Front Plant Sci. 2023 Aug 28;14:1226911. doi: 10.3389/fpls.2023.1226911. eCollection 2023.
10
Improving the genome editing efficiency of CRISPR/Cas9 in Arabidopsis and Medicago truncatula.提高 CRISPR/Cas9 在拟南芥和蒺藜苜蓿中的基因组编辑效率。
Planta. 2020 Jul 8;252(2):15. doi: 10.1007/s00425-020-03415-0.

引用本文的文献

1
Establishment and optimization of a tobacco rattle virus -based virus-induced gene Silencing in Atriplex canescens.基于烟草脆裂病毒的四翅滨藜病毒诱导基因沉默体系的建立与优化
Plant Methods. 2025 Aug 7;21(1):107. doi: 10.1186/s13007-025-01427-z.
2
Pigments to precision: RUBY aiding genetic transformation and genome editing in wheat and barley.精准色素:RUBY助力小麦和大麦的遗传转化与基因组编辑
Physiol Mol Biol Plants. 2025 Apr;31(4):545-554. doi: 10.1007/s12298-025-01591-5. Epub 2025 May 15.
3
Genome editing research initiatives and regulatory landscape of genome edited crops in India.印度基因组编辑作物的基因组编辑研究计划与监管格局
Transgenic Res. 2025 Mar 13;34(1):13. doi: 10.1007/s11248-025-00432-1.
4
CRISPR/Cas9 based genome editing of Phytoene desaturase (PDS) gene in chilli pepper (Capsicum annuum L.).基于CRISPR/Cas9对辣椒(Capsicum annuum L.)中八氢番茄红素去饱和酶(PDS)基因进行基因组编辑
J Genet Eng Biotechnol. 2024 Jun;22(2):100380. doi: 10.1016/j.jgeb.2024.100380. Epub 2024 Apr 30.

本文引用的文献

1
Genotypic variations for tuber nutrient content, dry matter and agronomic traits in tetraploid potato germplasm.四倍体马铃薯种质中块茎营养成分、干物质及农艺性状的基因型变异
Physiol Mol Biol Plants. 2022 Jun;28(6):1233-1248. doi: 10.1007/s12298-022-01197-1. Epub 2022 Jun 23.
2
CRISPR/Cas9 mediated disruption of () reduces phytic acid and improves iron and zinc accumulation in wheat grains.CRISPR/Cas9 介导的 () 基因敲除降低了小麦籽粒中的植酸含量,提高了铁锌的积累。
J Adv Res. 2021 Jul 14;37:33-41. doi: 10.1016/j.jare.2021.07.006. eCollection 2022 Mar.
3
CRISPR/Cas Genome Editing in Potato: Current Status and Future Perspectives.马铃薯中的CRISPR/Cas基因组编辑:现状与未来展望
Front Genet. 2022 Feb 2;13:827808. doi: 10.3389/fgene.2022.827808. eCollection 2022.
4
Optimization of Tissue Culturing and Genetic Transformation Protocol for .用于……的组织培养和遗传转化方案的优化
Front Plant Sci. 2022 Jan 21;12:784566. doi: 10.3389/fpls.2021.784566. eCollection 2021.
5
Potato biofortification: an effective way to fight global hidden hunger.马铃薯生物强化:对抗全球隐性饥饿的有效途径。
Physiol Mol Biol Plants. 2021 Oct;27(10):2297-2313. doi: 10.1007/s12298-021-01081-4. Epub 2021 Oct 7.
6
First Report of CRISPR/Cas9 Gene Editing in Mill.CRISPR/Cas9基因编辑在Mill中的首次报告
Front Plant Sci. 2021 Aug 25;12:728516. doi: 10.3389/fpls.2021.728516. eCollection 2021.
7
CRISPR/Cas9 Targeted Mutagenesis for Functional Genetics in Maize.用于玉米功能遗传学研究的CRISPR/Cas9靶向诱变
Plants (Basel). 2021 Apr 8;10(4):723. doi: 10.3390/plants10040723.
8
Optimizing the CRISPR/Cas9 system for genome editing in grape by using grape promoters.利用葡萄启动子优化用于葡萄基因组编辑的CRISPR/Cas9系统。
Hortic Res. 2021 Mar 1;8(1):52. doi: 10.1038/s41438-021-00489-z.
9
Genome editing in genes of tomatoes by non-selection method and of by one single guide RNA to edit two orthologs.通过非选择方法对番茄基因进行基因组编辑,以及使用单个引导RNA编辑两个直系同源基因。
Plant Biotechnol (Tokyo). 2020 Jun 25;37(2):213-221. doi: 10.5511/plantbiotechnology.20.0527b.
10
Creation of novel alleles of fragrance gene OsBADH2 in rice through CRISPR/Cas9 mediated gene editing.通过 CRISPR/Cas9 介导的基因编辑在水稻中创建新型香味基因 OsBADH2 等位基因。
PLoS One. 2020 Aug 12;15(8):e0237018. doi: 10.1371/journal.pone.0237018. eCollection 2020.

CRISPR/Cas9介导的重要主粮作物马铃薯中八氢番茄红素去饱和酶()基因的编辑。

CRISPR/Cas9-mediated editing of phytoene desaturase () gene in an important staple crop, potato.

作者信息

Siddappa Sundaresha, Sharma Neha, Salaria Neha, Thakur Kajal, Pathania Shruti, Singh Baljeet, Sharma Himani, Sood Salej, Bhardwaj Vinay, Thakur Ajay K, Mangal Vikas, Kumar Vinod, Muruthachallam Ravi, Singh Kashmir, Tuli Rakesh

机构信息

ICAR-Central Potato Research Institute, Shimla, H.P. 171001 India.

Indian Institute of Science Education and Research, Thiruvananthapuram, 695016 India.

出版信息

3 Biotech. 2023 May;13(5):129. doi: 10.1007/s13205-023-03543-w. Epub 2023 Apr 12.

DOI:10.1007/s13205-023-03543-w
PMID:37064007
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10097850/
Abstract

The gene editing using the CRISPR/Cas9 system has become an important biotechnological tool for studying gene function and improving crops. In this study, we have used CRISPR/Cas9 system for editing the phytoene desaturase gene () in popular Indian potato cultivar Kufri Chipsona-I. A construct (pHSE401) carrying two target gRNAs with glycine tRNA processing system under the control of Arabidopsis U6 promoter and the Cas9 protein was constructed and transformed in potato plants using -mediated genetic transformations. The regeneration efficiency of 45% was observed in regenerated plants, out of which 81% of the putative transformants shoot lines exhibited mutant or bleached phenotype (albinism). The deletion mutations were detected within the gene in the genotyped plants and a mutation efficiency of 72% for gRNA1 and gRNA2 has been detected using Sanger sequencing. Hence, we set up a CRISPR/Cas9-mediated genome editing protocol which is efficient and generates mutations (deletions) within gene in potato. The bleached phenotype is easily detectable after only few weeks after mediated transformation. This is the first report as a proof of concept for CRISPR/Cas9-based editing of gene in Indian potato cv. Kufri Chipsona-I. This study demonstrates that CRISPR/Cas9 can be used to edit genes at high frequency within the genome of the potato for various traits. Therefore, this study will aid in creating important mutants for modifying molecular mechanisms controlling traits of agronomic importance.

摘要

利用CRISPR/Cas9系统进行基因编辑已成为研究基因功能和改良作物的重要生物技术工具。在本研究中,我们使用CRISPR/Cas9系统对印度流行马铃薯品种库夫里薯片一号(Kufri Chipsona-I)中的八氢番茄红素去饱和酶基因()进行编辑。构建了一个携带两个靶向gRNA的载体(pHSE401),该载体带有在拟南芥U6启动子控制下的甘氨酸tRNA加工系统和Cas9蛋白,并通过介导的遗传转化将其导入马铃薯植株。在再生植株中观察到45%的再生效率,其中81%的推定转化体芽系表现出突变或白化表型(白化病)。在基因分型植株的基因内检测到缺失突变,使用桑格测序法检测到gRNA1和gRNA2的突变效率为72%。因此,我们建立了一种CRISPR/Cas9介导的基因组编辑方案,该方案高效且能在马铃薯基因内产生突变(缺失)。介导转化后仅几周就能轻松检测到白化表型。这是关于在印度马铃薯品种库夫里薯片一号中基于CRISPR/Cas9对基因进行编辑的概念验证的首次报道。本研究表明,CRISPR/Cas9可用于在马铃薯基因组内高频编辑各种性状的基因。因此,本研究将有助于创建重要突变体,以修饰控制具有农艺重要性性状的分子机制。