Wood Andrew J, Schulz Reiner, Woodfine Kathryn, Koltowska Katarzyna, Beechey Colin V, Peters Jo, Bourc'his Deborah, Oakey Rebecca J
Department of Medical and Molecular Genetics, King's College London, Guy's Hospital, London SE1 9RT, United Kingdom.
Genes Dev. 2008 May 1;22(9):1141-6. doi: 10.1101/gad.473408.
Maternally and paternally derived alleles can utilize different promoters, but allele-specific differences in cotranscriptional processes have not been reported. We show that alternative polyadenylation sites at a novel murine imprinted gene (H13) are utilized in an allele-specific manner. A differentially methylated CpG island separates polyA sites utilized on maternal and paternal alleles, and contains an internal promoter. Two genetic systems show that alleles lacking methylation generate truncated H13 transcripts that undergo internal polyadenylation. On methylated alleles, the internal promoter is inactive and elongation proceeds to downstream polyadenylation sites. This demonstrates that epigenetic modifications can influence utilization of alternative polyadenylation sites.
来自母本和父本的等位基因可以利用不同的启动子,但共转录过程中的等位基因特异性差异尚未见报道。我们发现,一个新的小鼠印记基因(H13)上的可变聚腺苷酸化位点以等位基因特异性方式被利用。一个差异甲基化的CpG岛将母本和父本等位基因上使用的聚腺苷酸化位点分开,并包含一个内部启动子。两个遗传系统表明,缺乏甲基化的等位基因会产生经历内部聚腺苷酸化的截短H13转录本。在甲基化的等位基因上,内部启动子无活性,延伸至下游聚腺苷酸化位点。这表明表观遗传修饰可影响可变聚腺苷酸化位点的利用。