Dindot Scott V, Farin Peter W, Farin Charlotte E, Romano Juan, Walker Shawn, Long Charles, Piedrahita Jorge A
Department of Veterinary Anatomy and Public Health, College of Veterinary Medicine, Texas A&M University, College Station, TX 77840, USA.
Biol Reprod. 2004 Aug;71(2):470-8. doi: 10.1095/biolreprod.103.025775. Epub 2004 Mar 24.
Somatic cell nuclear transfer (NT) in cattle is an inefficient process, whereby the production of calves is hindered by low pregnancy rates as well as fetal and placental abnormalities. Interspecies models have been previously used to facilitate the identification of single nucleotide polymorphisms (SNPs) within coding regions of genes to discriminate between parental alleles in the offspring. Here we report the use of a bovine interspecies model (Bos gaurus x Bos taurus) for the assessment and characterization of epigenetic modifications and genomic imprinting in Day 40-old female NT-derived fetuses and placenta. Analysis of NT and control pregnancies indicated disruption of genomic imprinting at the X inactivation-specific transcript (XIST) locus in the chorion, but not the fetus of clones, whereas proper allelic expression of the insulin-like growth factor II (IGF2) and gene trap locus 2 (GTL2) loci was maintained in both the fetus and placenta. Analysis of the XIST differentially methylated region (DMR) in clones indicated normal patterns of methylation; however, bisulfite sequencing of the satellite I repeat element and epidermal cytokeratin promoter indicated hypermethylation in the chorion of clones when compared with controls. No differences were detected in methylation levels in the fetus proper. These results indicate that the nuclear transfer process affects gene expression patterns in the trophectoderm- and inner cell mass-derived tissues to different extents.
牛的体细胞核移植(NT)是一个效率低下的过程,在此过程中,低妊娠率以及胎儿和胎盘异常阻碍了犊牛的生产。此前,种间模型已被用于促进对基因编码区域内单核苷酸多态性(SNP)的鉴定,以区分后代中的亲本等位基因。在此,我们报告使用一种牛种间模型(印度野牛×普通牛)来评估和表征40日龄雌性NT衍生胎儿和胎盘中的表观遗传修饰和基因组印记。对NT妊娠和对照妊娠的分析表明,绒毛膜中X染色体失活特异性转录本(XIST)位点的基因组印记受到破坏,但克隆胎儿未受影响,而胰岛素样生长因子II(IGF2)和基因陷阱位点2(GTL2)位点在胎儿和胎盘中均保持适当的等位基因表达。对克隆中XIST差异甲基化区域(DMR)的分析表明甲基化模式正常;然而,与对照相比,卫星I重复元件和表皮细胞角蛋白启动子的亚硫酸氢盐测序表明克隆绒毛膜中存在高甲基化。在胎儿本身的甲基化水平上未检测到差异。这些结果表明,核移植过程对滋养外胚层和内细胞团来源的组织中的基因表达模式有不同程度的影响。