Drmanac R, Nizetic D, Lennon G G, Beitverda A, Lehrach H
Genome Analysis Laboratory, Imperial Cancer Research Fund, London, UK.
Nucleic Acids Res. 1991 Nov 11;19(21):5839-42. doi: 10.1093/nar/19.21.5839.
A limitation to the use of oligonucleotide probes as tools for genetic and physical mapping has been the low hybridization positive frequency obtained by oligonucleotides of sufficient length to hybridize preferentially to cloned insert DNA (and not host E. coli genomic DNA). Both computer and experimental results now indicate that oligonucleotide probes composed of W (A or T) sequence are preferentially found in eukaryotic DNA, and can be used to provide high frequency, discriminative hybridization. Such W sequences may be useful as either probes or PCR primers in molecular diagnostic applications as well as in genetic and physical mapping.
将寡核苷酸探针用作遗传和物理图谱绘制工具的一个限制是,足够长度的寡核苷酸与克隆的插入DNA(而非宿主大肠杆菌基因组DNA)优先杂交时,杂交阳性频率较低。计算机和实验结果均表明,由W(A或T)序列组成的寡核苷酸探针优先存在于真核生物DNA中,可用于提供高频、特异性杂交。此类W序列在分子诊断应用以及遗传和物理图谱绘制中,作为探针或聚合酶链式反应(PCR)引物可能会很有用。