Park Kye-Yoon, Sellars Elizabeth A, Grinberg Alexander, Huang Sing-Ping, Pfeifer Karl
Laboratory of Mammalian Genes and Development, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892, USA.
Mol Cell Biol. 2004 May;24(9):3588-95. doi: 10.1128/MCB.24.9.3588-3595.2004.
Igf2 and H19 are coordinately regulated imprinted genes physically linked on the distal end of mouse chromosome 7. Genetic analyses demonstrate that the differentially methylated region (DMR) upstream of the H19 gene is necessary for three distinct functions: transcriptional insulation of the maternal Igf2 allele, transcriptional silencing of paternal H19 allele, and marking of the parental origin of the two chromosomes. To test the sufficiency of the DMR for the third function, we inserted DMR at two heterologous positions in the genome, downstream of H19 and at the alpha-fetoprotein locus on chromosome 5. Our results demonstrate that the DMR alone is sufficient to act as a mark of parental origin. Moreover, this activity is not dependent on germ line differences in DMR methylation. Thus, the DMR can mark its parental origin by a mechanism independent of its own DNA methylation.
Igf2和H19是在小鼠7号染色体远端物理相连的协同调控的印记基因。遗传分析表明,H19基因上游的差异甲基化区域(DMR)对于三种不同功能是必需的:母本Igf2等位基因的转录绝缘、父本H19等位基因的转录沉默以及两条染色体亲本来源的标记。为了测试DMR对于第三种功能的充分性,我们将DMR插入到基因组中的两个异源位置,即在H19下游和5号染色体上的甲胎蛋白基因座处。我们的结果表明,单独的DMR足以作为亲本来源的标记。此外,这种活性不依赖于DMR甲基化的种系差异。因此,DMR可以通过一种独立于其自身DNA甲基化的机制来标记其亲本来源。