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Fourteen Anonymous DNA Markers of Laboratory Rats Identified with Arbitrarily Primed Polymerase Chain Reaction (AP-PCR)

机译:通过任意引发的聚合酶链反应(AP-PCR)鉴定的实验大鼠的十四个匿名DNA标记

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In order to develop genetic markers in rats, arbitrarily primed polymerase chain reaction (AP-PCR) was performed with single primers originally designed for microsatellite loci, instead of primers with short-sized and arbitrary nucleotide sequences. Each primer generated reliable and reproducible segments under optimal conditions. The fourteen amplification products have been successfully mapped to rat chromosomes by either linkage analysis using backcross progeny or chromosomal assignment with somatic cell hybrids. All of the loci were located on different chromosomes from those of the microsatellite loci, suggesting that sequence-specifically designed single primers can produce anonymous segments of genomic DNA showing polymorphisms. These markers should contribute to finding linkages for traits of interest in rats.
机译:为了在大鼠中开发遗传标记,使用最初为微卫星基因座设计的单个引物,而不是短序列和任意核苷酸序列的引物,进行了任意引发的聚合酶链反应(AP-PCR)。在最佳条件下,每种引物均产生可靠且可重复的片段。通过使用回交后代的连锁分析或与体细胞杂种的染色体分配,已成功将这十四种扩增产物定位于大鼠染色体。所有的基因座都与微卫星基因座位于不同的染色体上,这表明序列特异性设计的单个引物可以产生显示多态性的基因组DNA匿名片段。这些标记物应有助于寻找大鼠中感兴趣的性状的连锁。

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