Park Joonghoon, Lai Liangxue, Samuel Melissa, Wax David, Bruno Richard S, French Richard, Prather Randall S, Yang Xiangzhong, Tian X Cindy
Center for Regenerative Biology, Department of Animal Science, University of Connecticut, Storrs, 06269, USA.
Cell Reprogram. 2011 Jun;13(3):215-23. doi: 10.1089/cell.2010.0088. Epub 2011 Mar 31.
Although numerous mammalian species have been successfully cloned by somatic cell nuclear transfer (SCNT), little is known about gene expression of cloned pigs by SCNT. In the present study, expression profiles of 1-month-old cloned pigs generated from fetal fibroblasts (n = 5) were compared to those of age-matched controls (n = 5) using a 13K oligonucleotide microarray. The brain, kidney, and lung were chosen for microarray analysis to represent tissues from endoderm, mesoderm, and ectoderm in origin. In clones, 179 and 154 genes were differentially expressed in the kidney and the lung, respectively (fold change >2, p < 0.05, false discovery rate = 0.05), whereas only seven genes were differentially expressed in the brain of clones. Functional analysis of the differentially expressed genes revealed that they were enriched in diabetic nephropathy in the kidney, delayed alveologenesis as well as downregulated MAPK signaling pathways in the lung, which was accompanied with collapsed alveoli in the histological examination of the lung. To evaluate whether the gene expression anomalies are associated with changes in DNA methylation, global concentration of the methylated cytosine was measured in lung DNA by HPLC. Clones were significantly hypermethylated (5.72%) compared to the controls (4.13%). Bisulfite-pyrosequencing analyses of the promoter regions of differentially expressed genes, MYC and Period 1 (PER1), however, did not show any differences in the degree of DNA methylation between controls and clones. Together, these findings demonstrate that cloned pigs have altered gene expression that may potentially cause organ dysfunction.
尽管通过体细胞核移植(SCNT)已成功克隆了许多哺乳动物物种,但对于通过SCNT克隆猪的基因表达情况却知之甚少。在本研究中,使用13K寡核苷酸微阵列将由胎儿成纤维细胞产生的1月龄克隆猪(n = 5)的表达谱与年龄匹配的对照猪(n = 5)进行了比较。选择脑、肾和肺进行微阵列分析,以代表内胚层、中胚层和外胚层来源的组织。在克隆猪中,分别有179个和154个基因在肾和肺中差异表达(倍数变化>2,p < 0.05,错误发现率 = 0.05),而在克隆猪的脑中只有7个基因差异表达。对差异表达基因的功能分析表明,它们在肾中富集于糖尿病肾病,在肺中富集于肺泡形成延迟以及丝裂原活化蛋白激酶(MAPK)信号通路下调,这在肺的组织学检查中伴有肺泡塌陷。为了评估基因表达异常是否与DNA甲基化变化有关,通过高效液相色谱法(HPLC)测量了肺DNA中甲基化胞嘧啶的总体浓度。与对照猪(4.13%)相比,克隆猪显著高甲基化(5.72%)。然而,对差异表达基因MYC和周期蛋白1(PER1)启动子区域的亚硫酸氢盐焦磷酸测序分析显示,对照猪和克隆猪之间的DNA甲基化程度没有任何差异。总之,这些发现表明克隆猪的基因表达发生了改变,这可能潜在地导致器官功能障碍。