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Re-investigation and RNA sequencing-based identification of genes with placenta-specific imprinted expression

机译:重新研究和基于RNA测序的具有胎盘特异性印迹表达的基因鉴定

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Within the vertebrate groups, only mammals are subject to a specialized epigenetic process termed genomic imprinting in which genes are preferentially expressed from one parental allele. Imprinted expression has been reported for >100 mouse genes and, for approximately one-quarter of these genes, the imprinted expression is specific to the placenta (or extraembryonic tissues). This seemingly placenta-specific imprinted expression has garnered much attention, as has the apparent lack of conserved imprinting between the human and mouse placenta. In this study, we used a novel approach to re-investigate the placenta-specific expression using embryo transfer and trophoblast stem cells. We analyzed 20 genes previously reported to show maternal allele-specific expression in the placenta, and only 8 genes were confirmed to be imprinted. Other genes were likely to be falsely identified as imprinted due to their relatively high expression in contaminating maternal cells. Next, we performed a genome-wide transcriptome assay and identified 133 and 955 candidate imprinted genes with paternal allele- and maternal allele-specific expression. Of those we analyzed in detail, 1/6 (Gab1) of the candidates for paternal allele-specific expression and only 1/269 (Ano1) candidates for maternal allele-specific expression were authentically imprinted genes. Imprinting of Ano1 and Gab1 was specific to the placenta and neither gene displayed allele-specific promoter DNA methylation. Imprinting of ANO1, but not GAB1, was conserved in the human placenta. Our findings impose a considerable revision of the current views of placental imprinting.
机译:在脊椎动物群中,只有哺乳动物要经历专门的表观遗传过程,称为基因组印迹,其中基因优先从一个亲本等位基因表达。已经报道了> 100种小鼠基因的印迹表达,并且对于这些基因的大约四分之一,印迹表达对胎盘(或胚外组织)具有特异性。这种看似胎盘特异性的印迹表达已引起了广泛的关注,人类和小鼠胎盘之间显然缺乏保守的印迹。在这项研究中,我们使用一种新颖的方法来重新研究使用胚胎移植和滋养层干细胞的胎盘特异性表达。我们分析了先前报道的显示胎盘中母体等位基因特异性表达的20个基因,只有8个基因被证实具有印记。由于其他基因在污染母体细胞中相对较高的表达,其他基因很可能被错误地鉴定为有印迹。接下来,我们进行了全基因组转录组测定,并鉴定了133和955个具有父本等位基因和母本等位基因特异性表达的候选印迹基因。在我们进行了详细分析的样本中,有1/6(Gab1)个是父本等位基因特异性表达的候选者,只有1/269(Ano1)个是母体等位基因特异性表达的候选者是真正印记的基因。 Ano1和Gab1的印迹是胎盘特有的,两个基因均未显示等位基因特异性启动子DNA甲基化。 ANO1,而不是GAB1,在人胎盘中的印记是保守的。我们的发现对当前的胎盘印记观点进行了相当大的修改。

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