Kijas J M, Fowler J C, Garbett C A, Thomas M R
School of Biological Sciences, Flinders University of South Australia.
Biotechniques. 1994 Apr;16(4):656-60, 662.
A method is described for the rapid isolation of microsatellite sequences using a biotin-labeled oligonucleotide attached to streptavidin-coated magnetic particles. The oligonucleotide "hook" in solution hybridizes to complementary single-stranded lengths of genomic DNA onto which have been engineered specific PCR priming sites. The final product is an enriched library of microsatellites of defined sequences. The method is applicable to any genome and in principle is adaptable to the rapid isolation of both repetitive as well as genic sequences. It is illustrated by the isolation of trinucleotide repeat (TAA)n sequences from the citrus genome.
描述了一种使用连接到链霉亲和素包被磁珠上的生物素标记寡核苷酸快速分离微卫星序列的方法。溶液中的寡核苷酸“钩子”与基因组DNA的互补单链长度杂交,在这些单链上已设计了特定的PCR引物位点。最终产物是一个富集的特定序列微卫星文库。该方法适用于任何基因组,原则上适用于重复序列和基因序列的快速分离。通过从柑橘基因组中分离三核苷酸重复序列(TAA)n进行了说明。