Urbański Dorian Fabian, Małolepszy Anna, Stougaard Jens, Andersen Stig Uggerhøj
Department of Molecular Biology and Genetics, Centre for Carbohydrate Recognition and Signalling, Aarhus University, Aarhus, Denmark.
Methods Mol Biol. 2013;1069:119-46. doi: 10.1007/978-1-62703-613-9_10.
The Lotus Retrotransposon 1 (LORE1) is used for genome-wide mutagenesis of the model legume Lotus japonicus. Characterization of the LORE1 insertion sites in individual mutant lines is critical for development and use of the resource. Here we present guidelines for use of the LORE1 reverse genetics resource and provide detailed protocols for insertion site identification and validation. For high-throughput identification of insertions in up to 9,216 pooled lines, the FSTpoolit protocol takes advantage of Splinkerette adapters, molecular barcoding, 2D pooling, Illumina sequencing, and automated data analysis using the freely available FSTpoolit software. Complementing the high-throughput approach, we describe a simplified sequence-specific amplification polymorphism (SSAP) protocol well suited for quick identification of insertion sites in a limited number of lines. Both the FSTpoolit and simplified SSAP protocols are generally applicable to insertion site identification in any insertional mutagenesis setup.
莲花逆转座子1(LORE1)用于模式豆科植物日本百脉根的全基因组诱变。单个突变体系中LORE1插入位点的特征分析对于该资源的开发和利用至关重要。在此,我们介绍了使用LORE1反向遗传学资源的指南,并提供了插入位点鉴定和验证的详细方案。为了高通量鉴定多达9216个混合品系中的插入情况,FSTpoolit方案利用了Splinkerette衔接子、分子条形码、二维混合、Illumina测序以及使用免费可得的FSTpoolit软件进行自动化数据分析。作为高通量方法的补充,我们描述了一种简化的序列特异性扩增多态性(SSAP)方案,非常适合在有限数量的品系中快速鉴定插入位点。FSTpoolit和简化的SSAP方案通常都适用于任何插入诱变设置中的插入位点鉴定。