Adam G, Mullen J A, Kindle K L
Plant Science Center, Cornell University, Ithaca, NY 14853-2703, USA.
Plant J. 1997 Jun;11(6):1349-58. doi: 10.1046/j.1365-313x.1997.11061349.x.
The utility of plant YAC libraries prepared in conventional YAC vectors would be dramatically increased if these YACs could be used directly for plant transformation. A pair of vectors that allow clones from YAC libraries to be modified (retrofitted) for plant transformation by direct DNA transfer methods, such as particle bombardment or electroporation, has been developed. Modification of the YAC is achieved in two sequential yeast transformation steps by taking advantage of the homologous recombination system in yeast. Using this approach, two plant-selectable marker genes and DNA sequence elements required for copy number amplification in yeast can be introduced into YACs present in yeast strain AB1380. The utility of these vectors is demonstrated by retrofitting YACs that contain inserts ranging in size from 80 to 700 kb. The 6- to 12-fold increase in copy number of these modified YACs facilitates the isolation of YAC DNA for direct DNA transformation methods. Retrofitted YACs were used for particle bombardment to examine the efficiency with which their large DNA inserts are transferred into plant cells. The availability of these retrofitting vectors should facilitate the transfer of YAC DNA inserts into plant cells and thus help bridge the gap between existing mapping techniques and plant transformation procedures.
如果能够直接将这些酵母人工染色体(YAC)用于植物转化,那么用传统YAC载体构建的植物YAC文库的效用将大大提高。现已开发出一对载体,可使YAC文库中的克隆通过粒子轰击或电穿孔等直接DNA转移方法进行改造(翻新),以用于植物转化。利用酵母中的同源重组系统,通过两个连续的酵母转化步骤实现对YAC的改造。采用这种方法,可以将两个植物选择标记基因以及酵母中拷贝数扩增所需的DNA序列元件引入酵母菌株AB1380中的YAC。通过翻新大小在80至700 kb之间的插入片段的YAC,证明了这些载体的效用。这些经过改造的YAC的拷贝数增加了6至12倍,便于分离用于直接DNA转化方法的YAC DNA。经过改造的YAC用于粒子轰击,以检测其大DNA插入片段转移到植物细胞中的效率。这些翻新载体的可用性应有助于将YAC DNA插入片段转移到植物细胞中,从而有助于弥合现有作图技术与植物转化程序之间的差距。