Lewis Michael W, Brant Jason O, Kramer Joseph M, Moss James I, Yang Thomas P, Hansen Peter J, Williams R Stan, Resnick James L
Department of Molecular Genetics and Microbiology, University of Florida College of Medicine, Gainesville, FL 32610-0266;
Department of Biochemistry and Molecular Biology, University of Florida College of Medicine, Gainesville, FL 32610-0245;
Proc Natl Acad Sci U S A. 2015 Jun 2;112(22):6871-5. doi: 10.1073/pnas.1411261111. Epub 2014 Nov 5.
Clusters of imprinted genes are often controlled by an imprinting center that is necessary for allele-specific gene expression and to reprogram parent-of-origin information between generations. An imprinted domain at 15q11-q13 is responsible for both Angelman syndrome (AS) and Prader-Willi syndrome (PWS), two clinically distinct neurodevelopmental disorders. Angelman syndrome arises from the lack of maternal contribution from the locus, whereas Prader-Willi syndrome results from the absence of paternally expressed genes. In some rare cases of PWS and AS, small deletions may lead to incorrect parent-of-origin allele identity. DNA sequences common to these deletions define a bipartite imprinting center for the AS-PWS locus. The PWS-smallest region of deletion overlap (SRO) element of the imprinting center activates expression of genes from the paternal allele. The AS-SRO element generates maternal allele identity by epigenetically inactivating the PWS-SRO in oocytes so that paternal genes are silenced on the future maternal allele. Here we have investigated functional activities of the AS-SRO, the element necessary for maternal allele identity. We find that, in humans, the AS-SRO is an oocyte-specific promoter that generates transcripts that transit the PWS-SRO. Similar upstream promoters were detected in bovine oocytes. This result is consistent with a model in which imprinting centers become DNA methylated and acquire maternal allele identity in oocytes in response to transiting transcription.
印记基因簇通常由一个印记中心控制,该印记中心对于等位基因特异性基因表达以及在世代间重新编程亲本来源信息是必需的。位于15q11 - q13的一个印记区域与安吉尔曼综合征(AS)和普拉德 - 威利综合征(PWS)这两种临床症状不同的神经发育障碍有关。安吉尔曼综合征源于该位点缺乏母源贡献,而普拉德 - 威利综合征则是由于父源表达基因的缺失所致。在一些罕见的普拉德 - 威利综合征和安吉尔曼综合征病例中,小的缺失可能导致亲本来源等位基因身份错误。这些缺失所共有的DNA序列定义了AS - PWS位点的一个双分型印记中心。印记中心的普拉德 - 威利综合征最小缺失重叠(SRO)元件激活父源等位基因的基因表达。安吉尔曼综合征SRO元件通过在卵母细胞中对普拉德 - 威利综合征SRO进行表观遗传失活来产生母源等位基因身份,从而使父源基因在未来的母源等位基因上沉默。在这里,我们研究了安吉尔曼综合征SRO的功能活性,它是产生母源等位基因身份所必需的元件。我们发现,在人类中,安吉尔曼综合征SRO是一个卵母细胞特异性启动子,它产生的转录本会穿过普拉德 - 威利综合征SRO。在牛卵母细胞中也检测到了类似的上游启动子。这一结果与一个模型一致,即印记中心会发生DNA甲基化,并在卵母细胞中响应转录通过而获得母源等位基因身份。