Petolino Joseph F, Arnold Nicole L
Discovery Research, Cell Biology, Dow AgroSciences LLC, Indianapolis, IN 46268, USA.
Methods Mol Biol. 2009;526:59-67. doi: 10.1007/978-1-59745-494-0_5.
There has been rapid progress in recent years in extending gene transfer capabilities to include plant species that fall outside the normal host range of Agrobacterium. Methods that allow direct DNA delivery into plant cells have contributed significantly to this expanded capability. Whiskers treatment is one means of delivering macromolecules, including DNA, to plant cells. Using relatively simple equipment and inexpensive materials, whiskers-mediated transformation of maize is possible. A critical prerequisite, however, is the establishment and maintenance of embryogenic tissue cultures as a source of totipotent, transformation-competent cells. Within hours of agitation in the presence of silicon carbide whiskers and DNA, embryogenic maize tissue cultures display transient gene expression, providing evidence for DNA uptake. Using appropriate selectable marker genes, following in vitro selection on inhibitory levels of a corresponding selection agent, stably transgenic tissue cultures can be generated from which fertile plants can be recovered. The timeline from whiskers treatment of embryogenic maize tissue cultures to fertile seed recovery is approximately 9 months, which is competitive with other methods of maize transformation.
近年来,在将基因转移能力扩展到农杆菌正常宿主范围之外的植物物种方面取得了迅速进展。允许将DNA直接导入植物细胞的方法对这种扩展能力做出了重大贡献。晶须处理是将包括DNA在内的大分子递送至植物细胞的一种手段。使用相对简单的设备和廉价的材料,就可以实现晶须介导的玉米转化。然而,一个关键的先决条件是建立和维持胚性组织培养物,作为全能、有转化能力细胞的来源。在碳化硅晶须和DNA存在下搅拌数小时内,胚性玉米组织培养物会显示瞬时基因表达,这为DNA摄取提供了证据。使用适当的选择标记基因,在对相应选择剂的抑制水平进行体外选择后,可以产生稳定的转基因组织培养物,并从中获得可育植株。从对胚性玉米组织培养物进行晶须处理到获得可育种子的时间线约为9个月,这与其他玉米转化方法相比具有竞争力。