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Agrobacterium ?¢????mediated transformation of the temperate grass Brachypodium distachyon (genotype Bd21) for T?¢????DNA insertional mutagenesis

机译:农杆菌介导的温带草短枝曲霉转化(Bd21基因型),用于T?DNA插入诱变

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Brachypodium distachyon is a promising model system for the structural and functional genomics of temperate grasses because of its physical, genetic and genome attributes. The sequencing of the inbred line Bd21 ( http://www.brachypodium.org ) started in 2007. However, a transformation method remains to be developed for the community standard line Bd21. In this article, a facile, efficient and rapid transformation system for Bd21 is described using Agrobacterium ?¢????mediated transformation of compact embryogenic calli (CEC) derived from immature embryos. Key features of this system include: (i) the use of the green fluorescent protein (GFP) associated with hygromycin selection for rapid identification of transgenic calli and plants; (ii) the desiccation of CEC after inoculation with Agrobacterium ; (iii) the utilization of Bd21 plants regenerated from tissue culture as a source of immature embryos; (iv) the control of the duration of the selection process; and (v) the supplementation of culture media with CuSO 4 prior to and during the regeneration of transgenic plants. Approximately 17% of CEC produced transgenic plants, enabling the generation of hundreds of T?¢????DNA insertion lines per experiment. GFP expression was observed in primary transformed Bd21 plants (T 0 ) and their progeny (T 1 ). The Mendelian inheritance of the transgenes was confirmed. An adaptor?¢????anchor strategy was developed for efficient retrieval of flanking sequence tags (FSTs) of T?¢????DNA inserts, and the resulting sequences are available in public databases. The production of T?¢????DNA insertion lines and the retrieval of associated FSTs reported here for the reference inbred line Bd21 will facilitate large?¢????scale functional genomics research in this model system.
机译:短枝曲霉因其物理,遗传和基因组属性而成为温带草的结构和功能基因组学的有前途的模型系统。自交系Bd21(http://www.brachypodium.org)的测序始于2007年。但是,社区标准系Bd21的转化方法仍有待开发。在本文中,描述了一种利用农杆菌介导的不成熟胚衍生的致密胚发生愈伤组织(CEC)转化Bd21的简便,有效和快速的系统。该系统的主要特征包括:(i)使用与潮霉素选择有关的绿色荧光蛋白(GFP)快速鉴定转基因愈伤组织和植物; (ii)接种农杆菌后干燥CEC; (iii)利用从组织培养中再生的Bd21植物作为未成熟胚的来源; (iv)控制甄选过程的持续时间; (v)在转基因植物再生之前和期间,用CuSO 4补充培养基。大约17%的CEC产生了转基因植物,每个实验可产生数百个Tα-β-DNA插入系。在初次转化的Bd21植物(T 0)及其后代(T 1)中观察到GFP表达。证实了转基因的孟德尔遗传。已经开发了一种衔接子锚定策略,以有效地检索Tβ-DNA插入物的侧翼序列标签(FST),并且所得序列可在公共数据库中获得。此处报道的用于参考自交系Bd21的TβDNA插入线的生产和相关FST的检索将有助于在此模型系统中进行大规模的功能基因组学研究。

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