Senda Sho, Wakayama Teruhiko, Arai Yoshikazu, Yamazaki Yukiko, Ohgane Jun, Tanaka Satoshi, Hattori Naka, Yanagimachi Ryuzo, Shiota Kunio
Laboratory of Cellular Biochemistry, Animal Resource Sciences/Veterinary Medical Sciences, The University of Tokyo, Bunkyo-ku, Tokyo 113-8657, Japan.
Cloning Stem Cells. 2007 Fall;9(3):293-302. doi: 10.1089/clo.2006.0050.
Cloned animals have various health problems. Aberrant DNA methylation is a possible cause of the problems. Restriction landmark genomic scanning (RLGS) that enabled us to analyze more than 1,000 CpG islands simultaneously demonstrated that all cloned newborns had aberrant DNA methylation. To study whether this aberration persists throughout the life of cloned individuals, we examined genome-wide DNA methylation status of newborn (19.5 dpc, n=2), adult (8-11 months old, n=3), and aged (23-27 months old, n=4) cloned mice using kidney cells as representatives. In the adult and aged groups, cloning was repeated using cumulus cells of the adult founder clone of each group as nucleus donor. Two newborn clones had three with aberrantly methylated loci, which is consistent with previous reports that all cloned newborns had DNA methylation aberrations. Interestingly, we could detect only one aberrantly methylated locus in two of the three adult clones in mid-age and none of four senescent clones, indicating that errors in DNA methylation disappear with advancement of animals' aging.
克隆动物存在各种健康问题。异常的DNA甲基化可能是这些问题的一个原因。能够同时分析1000多个CpG岛的限制性内切酶基因组扫描(RLGS)表明,所有克隆新生动物都存在异常的DNA甲基化。为了研究这种异常是否在克隆个体的整个生命过程中持续存在,我们以肾细胞为代表,检测了新生(19.5天胚龄,n = 2)、成年(8 - 11个月龄,n = 3)和老龄(23 - 27个月龄,n = 4)克隆小鼠的全基因组DNA甲基化状态。在成年组和老龄组中,使用每组成年供体克隆的卵丘细胞作为核供体重复进行克隆。两只新生克隆动物中有三只存在异常甲基化位点,这与之前所有克隆新生动物都存在DNA甲基化异常的报道一致。有趣的是,我们在三只成年中期克隆动物中的两只中仅检测到一个异常甲基化位点,而在四只老龄克隆动物中未检测到,这表明DNA甲基化错误随着动物年龄的增长而消失。