Kilger C, Pääbo S
Institute of Zoology, University of Munich, PO Box 202126, D-80021 Munich, Germany.
Nucleic Acids Res. 1997 May 15;25(10):2032-4. doi: 10.1093/nar/25.10.2032.
It is possible to perform a combined amplification and sequencing reaction ('DEXAS') directly from complex DNA mixtures by using two thermostable DNA polymerases, one that favours the incorporation of deoxynucleotides over dideoxynucleotides, and one which has a decreased ability to discriminate between these two nucleotide forms. During cycles of thermal denaturation, annealing and extension, the former enzyme primarily amplifies the target sequence whereas the latter enzyme primarily performs a sequencing reaction. This method allows the determination of single-copy nuclear DNA sequences from amounts of human genomic DNA comparable to those used to amplify nucleotide sequences by the polymerase chain reaction. Thus, DNA sequences can be easily determined directly from total genomic DNA.
通过使用两种热稳定DNA聚合酶,有可能直接从复杂的DNA混合物中进行联合扩增和测序反应(“DEXAS”),一种聚合酶优先掺入脱氧核苷酸而非双脱氧核苷酸,另一种聚合酶区分这两种核苷酸形式的能力降低。在热变性、退火和延伸循环过程中,前一种酶主要扩增靶序列,而后一种酶主要进行测序反应。该方法能够从与用于通过聚合酶链反应扩增核苷酸序列的量相当的人类基因组DNA量中确定单拷贝核DNA序列。因此,可以直接从总基因组DNA中轻松确定DNA序列。