Kubelik A R, Szabo L J
Cereal Rust Laboratory, Agricultural Research Service, U.S. Department of Agriculture, St. Paul, MN, USA.
Curr Genet. 1995 Sep;28(4):384-9. doi: 10.1007/BF00326438.
For genetic analysis of fungal DNAs, we have modified the RAPD method to use primers with G + C contents of 80-100%. In RAPD analysis of Puccinia graminis f. sp. tritici DNAs, these primers generated twice the number of both amplification products per primer and polymorphisms among isolates as compared to the standard 60-70% G + C primers. With respect to segregation and genetic similarity, RAPD markers generated by the high-GC primers behaved as do RAPD markers produced by the standard primers. These high-GC primers also yielded increased numbers of amplification products in RAPDs on the DNAs of a broad range of other fungi.
为了对真菌DNA进行遗传分析,我们对随机扩增多态性DNA(RAPD)方法进行了改进,使用鸟嘌呤(G)与胞嘧啶(C)含量为80%-100%的引物。在对小麦条锈菌DNA进行RAPD分析时,与标准的G+C含量为60%-70%的引物相比,这些引物产生的每个引物的扩增产物数量以及分离株之间的多态性均增加了一倍。就分离和遗传相似性而言,由高GC含量引物产生的RAPD标记的表现与标准引物产生的RAPD标记相同。这些高GC含量引物在对多种其他真菌的DNA进行RAPD分析时,也产生了更多的扩增产物。