• 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

利用 DNA 修复模板,通过锌指核酸酶介导的六倍体普通小麦(Triticum aestivum)内源基因的精确基因组编辑。

Zinc finger nuclease-mediated precision genome editing of an endogenous gene in hexaploid bread wheat (Triticum aestivum) using a DNA repair template.

机构信息

Genovo Biotechnology Co. Ltd, Tianjin, China.

Earlham Institute, Norwich Science Park, Norfolk, UK.

出版信息

Plant Biotechnol J. 2018 Dec;16(12):2088-2101. doi: 10.1111/pbi.12941. Epub 2018 May 28.

DOI:10.1111/pbi.12941
PMID:29734518
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6230953/
Abstract

Sequence-specific nucleases have been used to engineer targeted genome modifications in various plants. While targeted gene knockouts resulting in loss of function have been reported with relatively high rates of success, targeted gene editing using an exogenously supplied DNA repair template and site-specific transgene integration has been more challenging. Here, we report the first application of zinc finger nuclease (ZFN)-mediated, nonhomologous end-joining (NHEJ)-directed editing of a native gene in allohexaploid bread wheat to introduce, via a supplied DNA repair template, a specific single amino acid change into the coding sequence of acetohydroxyacid synthase (AHAS) to confer resistance to imidazolinone herbicides. We recovered edited wheat plants having the targeted amino acid modification in one or more AHAS homoalleles via direct selection for resistance to imazamox, an AHAS-inhibiting imidazolinone herbicide. Using a cotransformation strategy based on chemical selection for an exogenous marker, we achieved a 1.2% recovery rate of edited plants having the desired amino acid change and a 2.9% recovery of plants with targeted mutations at the AHAS locus resulting in a loss-of-function gene knockout. The latter results demonstrate a broadly applicable approach to introduce targeted modifications into native genes for nonselectable traits. All ZFN-mediated changes were faithfully transmitted to the next generation.

摘要

序列特异性核酸酶已被用于对各种植物进行靶向基因组修饰。虽然通过相对较高的成功率报告了导致功能丧失的靶向基因敲除,但使用外源 DNA 修复模板和位点特异性转基因整合的靶向基因编辑更具挑战性。在这里,我们报告了锌指核酸酶 (ZFN) 介导的非同源末端连接 (NHEJ) 靶向编辑异源六倍体面包小麦内源基因的首次应用,通过提供的 DNA 修复模板,将特定的单个氨基酸变化引入到编码序列的乙酰羟酸合酶 (AHAS) 中,以赋予对咪唑啉酮除草剂的抗性。我们通过直接选择对 AHAS 抑制剂咪唑啉酮除草剂 imazamox 的抗性,从一个或多个 AHAS 同系物中回收了具有靶向氨基酸修饰的编辑小麦植物。使用基于化学选择外源标记的共转化策略,我们实现了具有所需氨基酸变化的编辑植物的 1.2%恢复率,以及在 AHAS 基因座上具有靶向突变导致功能丧失基因敲除的植物的 2.9%恢复率。后者的结果证明了一种广泛适用于引入非选择性性状的内源基因的靶向修饰的方法。所有 ZFN 介导的变化都被准确地传递到下一代。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bb1/11388573/ecc889964206/PBI-16-2088-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bb1/11388573/3ae6993066e1/PBI-16-2088-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bb1/11388573/3c58ea3c948d/PBI-16-2088-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bb1/11388573/a2d6142d6ce9/PBI-16-2088-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bb1/11388573/ecc889964206/PBI-16-2088-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bb1/11388573/3ae6993066e1/PBI-16-2088-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bb1/11388573/3c58ea3c948d/PBI-16-2088-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bb1/11388573/a2d6142d6ce9/PBI-16-2088-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bb1/11388573/ecc889964206/PBI-16-2088-g003.jpg

相似文献

1
Zinc finger nuclease-mediated precision genome editing of an endogenous gene in hexaploid bread wheat (Triticum aestivum) using a DNA repair template.利用 DNA 修复模板,通过锌指核酸酶介导的六倍体普通小麦(Triticum aestivum)内源基因的精确基因组编辑。
Plant Biotechnol J. 2018 Dec;16(12):2088-2101. doi: 10.1111/pbi.12941. Epub 2018 May 28.
2
Zinc finger nuclease-mediated targeting of multiple transgenes to an endogenous soybean genomic locus via non-homologous end joining.锌指核酸酶介导的非同源末端连接靶向多个转基因到大豆内源基因组位点。
Plant Biotechnol J. 2019 Apr;17(4):750-761. doi: 10.1111/pbi.13012. Epub 2018 Oct 15.
3
Efficient and transgene-free genome editing in wheat through transient expression of CRISPR/Cas9 DNA or RNA.通过瞬时表达 CRISPR/Cas9 DNA 或 RNA 在小麦中进行高效且无转基因的基因组编辑。
Nat Commun. 2016 Aug 25;7:12617. doi: 10.1038/ncomms12617.
4
Plant Biotechnology Applications of Zinc Finger Technology.锌指技术的植物生物技术应用
Methods Mol Biol. 2019;1864:295-310. doi: 10.1007/978-1-4939-8778-8_20.
5
Genome editing in wheat microspores and haploid embryos mediated by delivery of ZFN proteins and cell-penetrating peptide complexes.小麦小孢子和单倍体胚中通过递送 ZFN 蛋白和细胞穿透肽复合物进行基因组编辑。
Plant Biotechnol J. 2020 May;18(5):1307-1316. doi: 10.1111/pbi.13296. Epub 2019 Dec 3.
6
Trait stacking via targeted genome editing.通过靶向基因组编辑进行性状叠加。
Plant Biotechnol J. 2013 Dec;11(9):1126-34. doi: 10.1111/pbi.12107. Epub 2013 Aug 19.
7
TALEN-Mediated Homologous Recombination Produces Site-Directed DNA Base Change and Herbicide-Resistant Rice.TALEN 介导的同源重组产生靶向 DNA 碱基改变和除草剂抗性水稻。
J Genet Genomics. 2016 May 20;43(5):297-305. doi: 10.1016/j.jgg.2016.03.005. Epub 2016 Mar 22.
8
From Genetic Stock to Genome Editing: Gene Exploitation in Wheat.从遗传资源到基因组编辑:小麦中的基因利用。
Trends Biotechnol. 2018 Feb;36(2):160-172. doi: 10.1016/j.tibtech.2017.10.002. Epub 2017 Nov 5.
9
Introgression of an imidazolinone-resistance gene from winter wheat (Triticum aestivum L.) into jointed goatgrass (Aegilops cylindrica Host).将冬小麦(普通小麦)中的咪唑啉酮抗性基因渗入节节麦(圆柱山羊草)。
Theor Appl Genet. 2006 Dec;114(1):177-86. doi: 10.1007/s00122-006-0421-0. Epub 2006 Oct 21.
10
Designed nucleases for targeted genome editing.用于靶向基因组编辑的设计核酸酶。
Plant Biotechnol J. 2016 Feb;14(2):448-62. doi: 10.1111/pbi.12465. Epub 2015 Sep 15.

引用本文的文献

1
Advances in genome editing in plants within an evolving regulatory landscape, with a focus on its application in wheat breeding.植物基因组编辑在不断演变的监管环境中的进展,重点关注其在小麦育种中的应用。
J Plant Biochem Biotechnol. 2025;34(3):599-614. doi: 10.1007/s13562-025-00981-w. Epub 2025 Apr 15.
2
Agricultural biotechnology in China: product development, commercialization, and perspectives.中国的农业生物技术:产品开发、商业化及前景
aBIOTECH. 2025 May 15;6(2):284-310. doi: 10.1007/s42994-025-00209-4. eCollection 2025 Jun.
3
Evolution of agricultural biotechnology is the paradigm shift in crop resilience and development: a review.

本文引用的文献

1
Generation of a Collection of Mutant Tomato Lines Using Pooled CRISPR Libraries.利用混合CRISPR文库生成突变番茄系集合
Plant Physiol. 2017 Aug;174(4):2023-2037. doi: 10.1104/pp.17.00489. Epub 2017 Jun 23.
2
CRISPR-Cas9 Targeted Mutagenesis Leads to Simultaneous Modification of Different Homoeologous Gene Copies in Polyploid Oilseed Rape ().CRISPR-Cas9靶向诱变导致多倍体油菜中不同同源基因拷贝的同时修饰()。
Plant Physiol. 2017 Jun;174(2):935-942. doi: 10.1104/pp.17.00426. Epub 2017 Apr 18.
3
Mechanisms of precise genome editing using oligonucleotide donors.
农业生物技术的演变:作物抗逆性与发育的范式转变综述
Front Plant Sci. 2025 Jun 19;16:1585826. doi: 10.3389/fpls.2025.1585826. eCollection 2025.
4
Enhancing wheat resilience: biotechnological advances in combating heat stress and environmental challenges.增强小麦抗逆性:应对热胁迫和环境挑战的生物技术进展
Plant Mol Biol. 2025 Mar 9;115(2):41. doi: 10.1007/s11103-025-01569-7.
5
Advancing crop disease resistance through genome editing: a promising approach for enhancing agricultural production.通过基因组编辑提升作物抗病性:一种提高农业产量的有前景的方法。
Front Genome Ed. 2024 Jun 26;6:1399051. doi: 10.3389/fgeed.2024.1399051. eCollection 2024.
6
Genome Editing Approaches Using Zinc Finger Nucleases (ZFNs) for the Treatment of Motor Neuron Diseases.使用锌指核酸酶(ZFNs)治疗运动神经元疾病的基因组编辑方法
Curr Pharm Biotechnol. 2024 Jun 6. doi: 10.2174/0113892010307288240526071810.
7
Metabolic engineering of plant secondary metabolites: prospects and its technological challenges.植物次生代谢产物的代谢工程:前景及其技术挑战。
Front Plant Sci. 2023 May 12;14:1171154. doi: 10.3389/fpls.2023.1171154. eCollection 2023.
8
Unclasping potentials of genomics and gene editing in chickpea to fight climate change and global hunger threat.鹰嘴豆基因组学和基因编辑在应对气候变化和全球饥饿威胁方面的潜力释放。
Front Genet. 2023 Apr 18;14:1085024. doi: 10.3389/fgene.2023.1085024. eCollection 2023.
9
A CRISPR way for accelerating cereal crop improvement: Progress and challenges.一种加速谷类作物改良的CRISPR方法:进展与挑战
Front Genet. 2023 Jan 6;13:866976. doi: 10.3389/fgene.2022.866976. eCollection 2022.
10
Genomics and transcriptomics to protect rice ( L.) from abiotic stressors: -pathways to achieving zero hunger.利用基因组学和转录组学保护水稻免受非生物胁迫:实现零饥饿的途径
Front Plant Sci. 2022 Oct 20;13:1002596. doi: 10.3389/fpls.2022.1002596. eCollection 2022.
使用寡核苷酸供体进行精确基因组编辑的机制。
Genome Res. 2017 Jul;27(7):1099-1111. doi: 10.1101/gr.214775.116. Epub 2017 Mar 29.
4
Characteristics of Genome Editing Mutations in Cereal Crops.作物基因组编辑突变的特征。
Trends Plant Sci. 2017 Jan;22(1):38-52. doi: 10.1016/j.tplants.2016.08.009. Epub 2016 Sep 17.
5
Gene replacements and insertions in rice by intron targeting using CRISPR-Cas9.利用 CRISPR-Cas9 通过内含子靶向在水稻中进行基因替换和插入。
Nat Plants. 2016 Sep 12;2:16139. doi: 10.1038/nplants.2016.139.
6
Applications of CRISPR/Cas9 technology for targeted mutagenesis, gene replacement and stacking of genes in higher plants.CRISPR/Cas9技术在高等植物中用于靶向诱变、基因替换和基因堆叠的应用。
Plant Cell Rep. 2016 Jul;35(7):1439-50. doi: 10.1007/s00299-016-1989-8. Epub 2016 May 4.
7
The expanding footprint of CRISPR/Cas9 in the plant sciences.CRISPR/Cas9在植物科学领域不断扩大的影响力。
Plant Cell Rep. 2016 Jul;35(7):1451-68. doi: 10.1007/s00299-016-1987-x. Epub 2016 Apr 30.
8
Homology-based double-strand break-induced genome engineering in plants.基于同源性的双链断裂诱导的植物基因组工程。
Plant Cell Rep. 2016 Jul;35(7):1429-38. doi: 10.1007/s00299-016-1981-3. Epub 2016 Apr 15.
9
Gene targeting and transgene stacking using intra genomic homologous recombination in plants.利用植物基因组内同源重组进行基因靶向和转基因堆叠
Plant Methods. 2016 Feb 1;12:11. doi: 10.1186/s13007-016-0111-0. eCollection 2016.
10
ssODN-mediated knock-in with CRISPR-Cas for large genomic regions in zygotes.利用CRISPR-Cas系统通过单链寡脱氧核苷酸介导在受精卵中对大片段基因组区域进行基因敲入。
Nat Commun. 2016 Jan 20;7:10431. doi: 10.1038/ncomms10431.