Toyota M, Ushijima T, Suzui M, Murakumo Y, Imai K, Sugimura T, Matsuyama M
Carcinogenesis Division, National Cancer Center Research Institute, Tokyo 104, 5-1-1, Tsukiji, Chuo-ku, Japan.
Mamm Genome. 1998 Sep;9(9):735-9. doi: 10.1007/s003359900854.
To obtain genetic markers linked to a specific genetic locus, genomic subtraction with a DNA pool of backcross or F2 intercross animals with a specific genotype at the locus is known to be effective. To determine whether the pooling strategy is also effective for isolation of genetic markers linked to a quantitative phenotype that can potentially be controlled by multiple genetic loci, we tested the ability of representational difference analysis (RDA) to isolate genetic markers linked to the thymus enlargement observed in the BUF/Mna (BUF) rat. This is known to be controlled by single major and minor genes, Ten1 and Ten2, on Chromosomes (Chrs) 1 and 13, respectively, both of which have dose effects on the normal WKY/Ncj (WKY) allele. DNA from an inbred WKY rat was used as the tester, and the driver was prepared from a DNA pool of 12 (WKY x BUF)F1 x BUF backcross rats with high thymus ratios (thymus weight/body weight), expected to have dominance of the BUF allele in the responsible loci. By two RDA series with the restriction enzymes BglII and BamHI, respectively, 28 polymorphic markers were isolated, and 8 of them were shown to be linked to Ten1, and one to Ten2. One of the 8 markers linked to Ten1 demonstrated no recombination in 18 rats with high thymus ratios. RDA with a DNA pool based on a quantitative phenotype (phenotype-directed RDA) can thus be considered an efficient approach for direct isolation of polymorphic markers linked to a quantitative trait.
为了获得与特定基因座连锁的遗传标记,已知利用在该基因座具有特定基因型的回交或F2杂交动物的DNA池进行基因组消减是有效的。为了确定这种混合策略对于分离与可能受多个基因座控制的数量性状连锁的遗传标记是否也有效,我们测试了代表性差异分析(RDA)分离与BUF/Mna(BUF)大鼠中观察到的胸腺肿大相关的遗传标记的能力。已知这分别受位于1号和13号染色体上的单个主基因和次要基因Ten1和Ten2控制,这两个基因对正常的WKY/Ncj(WKY)等位基因都有剂量效应。将近交WKY大鼠的DNA用作测试者,驱动者由12只胸腺比例高(胸腺重量/体重)的(WKY×BUF)F1×BUF回交大鼠的DNA池制备,预期在相关基因座中BUF等位基因占优势。分别用限制性内切酶BglII和BamHI进行两个RDA系列分析,分离出28个多态性标记,其中8个与Ten1连锁,1个与Ten2连锁。与Ten1连锁的8个标记之一在18只胸腺比例高的大鼠中未显示重组。因此,基于数量性状的DNA池进行RDA(表型导向RDA)可被认为是直接分离与数量性状连锁的多态性标记的有效方法。