首页> 美国卫生研究院文献>Scientific Reports >Simple rapid and efficient transformation of genotype Nisqually-1: a basic tool for the first sequenced model tree
【2h】

Simple rapid and efficient transformation of genotype Nisqually-1: a basic tool for the first sequenced model tree

机译:基因型Nisqually-1的简单快速和高效转化:第一个测序模型树的基本工具

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Genotype Nisqually-1 is the first model woody plant with an available well-annotated genome. Nevertheless, a simple and rapid transformation of Nisqually-1 remains to be established. Here, we developed a novel shoot regeneration method for Nisqually-1 using leaf petiole and stem segment explants. Numerous shoots formed in the incision of explants within two weeks. The optimized shoot regeneration medium (SRM) contained 0.03 mg l−1 6-benzylaminopurine, 0.02 mg l−1 indole-3-butyric acid and 0.0008 mg l−1 thidiazuron. Based on this, Agrobacterium-mediated genetic transformation of stem explants was examined using the vector pBI121 that contains the β-glucuronidase (GUS) as a reporter gene. Consequently, factors affecting transformation frequency of GUS-positive shoots were optimized as follows: Agrobacteria cell suspension with an OD600 of 0.4, 20 min infection time, 2 days of co-cultivation duration and the addition of 80 µM acetosyringone into Agrobacteria infective suspension and co-cultivation SRM. Using this optimized method, transgenic plantlets of Nisqually-1 – with an average transformation frequency of 26.7% – were obtained with 2 months. Southern blot and GUS activity staining confirmed the integration of the foreign GUS gene into Nisqually-1. This novel transformation system for Nisqually-1 was rapid, efficient, and simple to operate and will improve more genetic applications in this model tree.
机译:基因型Nisqually-1是第一个具有可用注释良好的基因组的模型木本植物。尽管如此,仍需要建立Nisqually-1的简单快速转换。在这里,我们开发了一种使用叶柄和茎段外植体对Nisqually-1进行新芽再生的方法。两周内在外植体切口中形成许多芽。优化的芽再生培养基(SRM)含有0.03 mg l -1 6-苄氨基嘌呤,0.02 mg l -1 吲哚-3-丁酸和0.0008 mg l -1 噻唑隆。基于此,使用含有β-葡糖醛酸糖苷酶(GUS)作为报告基因的载体pBI121检查了农杆菌介导的干外植体的遗传转化。因此,对影响GUS阳性芽转化频率的因素进行了如下优化:OD600为0.4的农杆菌细胞悬液,感染时间20µmin,共培养2天,以及在农杆菌感染性悬液和大肠杆菌中添加80µµM乙酰丁香酮。培养SRM。使用这种优化方法,在2个月内获得了Nisqually-1的转基因植株-平均转化率为26.7%。 Southern印迹和GUS活性染色证实了外源GUS基因已整合到Nisqually-1中。 Nisqually-1的这种新型转化系统快速,高效且易于操作,并将改善该模型树中的更多遗传应用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号