Smith R J, Kelsey G
Developmental Genetics Programme, The Babraham Institute, Babraham, Cambridge, UK.
Methods Mol Biol. 2001;181:113-32. doi: 10.1385/1-59259-211-2:113.
The technique of representational difference analysis (RDA) was originally described by Lisitsyn et al. (1993) as a means of identifying differences between complex genomes by the use of subtractive hybridisation (1). This protocol for methylation-sensitive RDA (Me-RDA) describes adaptations to the original technique that, by the use of oligonucleotides for HpaII or Hin6I sites, allow the identification of sequences whose methylation differs between two sources of DNA. Differences in the methylation of the maternal and paternal alleles of imprinted genes have been described for most imprinted genes studied to date (2). The importance of methylation in the control of imprinted gene expression has been clearly demonstrated by the perturbation of allelic expression in mice deficient in Dnmt1, the major mammalian DNA methyltransferase (3), and methylation has been suggested to fulfill the necessary requirements of an "imprint" (4).
代表性差异分析(RDA)技术最初由利西琴等人(1993年)描述为一种通过消减杂交来识别复杂基因组之间差异的方法(1)。本甲基化敏感RDA(Me-RDA)方案描述了对原始技术的改进,通过使用针对HpaII或Hin6I位点的寡核苷酸,能够识别在两个DNA来源之间甲基化存在差异的序列。对于迄今为止研究的大多数印记基因,已报道了印记基因母本和父本等位基因甲基化的差异(2)。在缺乏主要哺乳动物DNA甲基转移酶Dnmt1的小鼠中,等位基因表达受到干扰,这清楚地证明了甲基化在印记基因表达调控中的重要性(3),并且有人提出甲基化满足了“印记”的必要条件(4)。