Yamazaki Wataru, Amano Tomoko, Bai Hanako, Takahashi Masashi, Kawahara Manabu
From the Laboratory of Animal Genetics and Reproduction, Research Faculty of Agriculture, Hokkaido University, Kita-9, Nishi-9, Kita-ku, Sapporo 060-8589 and.
the Laboratory of Animal Genetics, Department of Sustainable Agriculture, College of Agriculture, Food and Environmental Science, Rakuno Gakuen University, Bunkyodai-Midorimachi, Ebetsu, Hokkaido 069-8501, Japan.
J Biol Chem. 2016 Sep 30;291(40):20924-20931. doi: 10.1074/jbc.M116.744144. Epub 2016 Aug 16.
Genomic imprinting is an epigenetic mechanism that switches the expression of imprinted genes involved in normal embryonic growth and development in a parent-of-origin-specific manner. Changes in DNA methylation statuses from polyploidization are a well characterized epigenetic modification in plants. However, how changes in ploidy affect both imprinted gene expression and methylation status in mammals remains unclear. To address this, we used quantitative real time PCR to analyze expression levels of imprinted genes in mouse tetraploid fetuses. We used bisulfite sequencing to assess the methylation statuses of differentially methylated regions (DMRs) that regulate imprinted gene expression in triploid and tetraploid fetuses. The nine imprinted genes H19, Gtl2, Dlk1, Igf2r, Grb10, Zim1, Peg3, Ndn, and Ipw were all unregulated; in particular, the expression of Zim1 was more than 10-fold higher, and the expression of Ipw was repressed in tetraploid fetuses. The methylation statuses of four DMRs H19, intergenic (IG), Igf2r, and Snrpn in tetraploid and triploid fetuses were similar to those in diploid fetuses. We also performed allele-specific RT-PCR sequencing to determine the alleles expressing the three imprinted genes Igf2, Gtl2, and Dlk1 in tetraploid fetuses. These three imprinted genes showed monoallelic expression in a parent-of-origin-specific manner. Expression of non-imprinted genes regulating neural cell development significantly decreased in tetraploid fetuses, which might have been associated with unregulated imprinted gene expression. This study provides the first detailed analysis of genomic imprinting in tetraploid fetuses, suggesting that imprinted gene expression is disrupted, but DNA methylation statuses of DMRs are stable following changes in ploidy in mammals.
基因组印记是一种表观遗传机制,它以亲本来源特异性的方式调控参与正常胚胎生长和发育的印记基因的表达。多倍体化导致的DNA甲基化状态变化是植物中一种特征明确的表观遗传修饰。然而,倍性变化如何影响哺乳动物的印记基因表达和甲基化状态仍不清楚。为了解决这个问题,我们使用定量实时PCR分析了小鼠四倍体胎儿中印记基因的表达水平。我们使用亚硫酸氢盐测序来评估三倍体和四倍体胎儿中调控印记基因表达的差异甲基化区域(DMR)的甲基化状态。九个印记基因H19、Gtl2、Dlk1、Igf2r、Grb10、Zim1、Peg3、Ndn和Ipw均未受调控;特别是,Zim1的表达增加了10倍以上,而Ipw的表达在四倍体胎儿中受到抑制。四倍体和三倍体胎儿中四个DMR(H19、基因间区(IG)、Igf2r和Snrpn)的甲基化状态与二倍体胎儿相似。我们还进行了等位基因特异性RT-PCR测序,以确定四倍体胎儿中表达三个印记基因Igf2、Gtl2和Dlk1的等位基因。这三个印记基因以亲本来源特异性的方式呈现单等位基因表达。调控神经细胞发育的非印记基因的表达在四倍体胎儿中显著降低,这可能与印记基因表达失控有关。这项研究首次对四倍体胎儿的基因组印记进行了详细分析,表明印记基因表达受到破坏,但哺乳动物倍性变化后DMR的DNA甲基化状态是稳定的。