Strizhov Nicolai, Li Yong, Rosso Mario G, Viehoever Prisca, Dekker Koen A, Weisshaar Bernd
Max Planck Institute for Plant Breeding Research, Cologne, Germany.
Biotechniques. 2003 Dec;35(6):1164-8. doi: 10.2144/03356st01.
A pipeline has been created for the characterization of Arabidopsis thaliana mutants by generating flanking sequence tags (FSTs) and optimized for economic, high-throughput production. The GABI-Kat collection of T-DNA mutagenized A. thaliana plants was used as a source of independent transgenic lines. The pipeline included robotized extraction of genomic DNA in a 96-well format, an adapter-ligation PCR method for amplification of plant sequences adjacent to T-DNA borders, automated purification and sequencing of PCR products, and computational trimming of the resulting sequence files. Data quality was significantly improved by (i) restriction digestion of the adaptor-ligation products to reduce trivial sequences caused by co-amplification of fragments derived from the free plasmid, and (ii) the design of the adaptor primers for the second amplification step to enhance selective generation of single PCR fragments, even from lines with multiple T-DNA insertions. Gel-purification was avoided by including these steps, the number of amplification reactions per line was reduced from four to three, and the percentage of lines that yielded at least one FST was increased from 66% to 86%. More than 58,000 FSTs have been submitted to GenBank and are available at http://www.mpiz-koeln.mpg.de/GABI-Kat/.
通过生成侧翼序列标签(FST),已建立了一种用于拟南芥突变体表征的流程,并针对经济高效的高通量生产进行了优化。使用T-DNA诱变的拟南芥植物的GABI-Kat文库作为独立转基因系的来源。该流程包括以96孔格式自动提取基因组DNA、用于扩增T-DNA边界附近植物序列的衔接子连接PCR方法、PCR产物的自动纯化和测序,以及对所得序列文件进行计算修剪。通过以下方式显著提高了数据质量:(i)对衔接子连接产物进行限制性消化,以减少由游离质粒衍生片段的共扩增导致的琐碎序列;(ii)设计用于第二步扩增的衔接子引物,以增强单PCR片段的选择性生成,即使是来自具有多个T-DNA插入的品系。通过纳入这些步骤避免了凝胶纯化,每个品系的扩增反应数量从四个减少到三个,产生至少一个FST的品系百分比从66%提高到86%。超过58,000个FST已提交至GenBank,可在http://www.mpiz-koeln.mpg.de/GABI-Kat/获取。