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利用草甘膦选择,通过农杆菌介导对小麦(普通小麦)进行大规模转化

Agrobacterium-mediated large-scale transformation of wheat (Triticum aestivum L.) using glyphosate selection.

作者信息

Hu T, Metz S, Chay C, Zhou H P, Biest N, Chen G, Cheng M, Feng X, Radionenko M, Lu F, Fry J

机构信息

Monsanto Company, 700 Chesterfield Parkway West, St. Louis, MO 63017, USA.

出版信息

Plant Cell Rep. 2003 Jun;21(10):1010-19. doi: 10.1007/s00299-003-0617-6. Epub 2003 Apr 12.

DOI:10.1007/s00299-003-0617-6
PMID:12835912
Abstract

An Agrobacterium-mediated transformation system with glyphosate selection has been developed for the large-scale production of transgenic plants. The system uses 4-day precultured immature embryos as explants. A total of 30 vectors containing the 5-enol-pyruvylshikimate-3-phosphate synthase gene from Agrobacterium strain CP4 (aroA:CP4), which confers resistance to glyphosate, were introduced into wheat using this system. The aroA:CP4 gene served two roles in this study-selectable marker and gene of interest. More than 3,000 transgenic events were produced with an average transformation efficiency of 4.4%. The entire process from isolation of immature embryos to production of transgenic plantlets was 50-80 days. Transgenic events were evaluated over several generations based on genetic, agronomic and molecular criteria. Forty-six percent of the transgenic events fit a 3:1 segregation ratio. Molecular analysis confirmed that four of six lead transgenic events selected from Agrobacterium transformation contained a single insert and a single copy of the transgene. Stable expression of theAROA:CP4 gene was confirmed by ELISA through nine generations. A comparison of Agrobacterium-mediated transformation to a particle bombardment system demonstrated that the Agrobacterium system is reproducible, has a higher transformation efficiency with glyphosate selection and produces higher quality transgenic events in wheat. One of the lead events from this study, no. 33391, has been identified as a Roundup Ready wheat commercial candidate.

摘要

已开发出一种带有草甘膦选择的农杆菌介导转化系统,用于大规模生产转基因植物。该系统使用预培养4天的未成熟胚作为外植体。利用此系统将总共30个含有来自农杆菌菌株CP4的5-烯醇式丙酮酸莽草酸-3-磷酸合酶基因(aroA:CP4)的载体导入小麦,该基因赋予对草甘膦的抗性。aroA:CP4基因在本研究中发挥了两个作用——选择标记和目的基因。产生了3000多个转基因事件,平均转化效率为4.4%。从未成熟胚分离到转基因植株再生的整个过程为50 - 80天。基于遗传、农艺和分子标准对转基因事件进行了多代评估。46%的转基因事件符合3:1的分离比例。分子分析证实,从农杆菌转化中选出的6个主要转基因事件中有4个含有单个插入片段和单个转基因拷贝。通过ELISA在九代中证实了AROA:CP4基因的稳定表达。农杆菌介导转化与粒子轰击系统的比较表明,农杆菌系统具有可重复性,在草甘膦选择下具有更高的转化效率,并且在小麦中产生更高质量的转基因事件。本研究中的一个主要事件,编号33391,已被确定为抗草甘膦小麦商业候选品种。

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