Department of Genetics and Cell Biology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima 734-8553, Japan.
Cells. 2020 Jan 17;9(1):239. doi: 10.3390/cells9010239.
Chromosomal segregation errors in germ cells and early embryonic development underlie aneuploidies, which are numerical chromosomal abnormalities causing fetal absorption, developmental anomalies, and carcinogenesis. It has been considered that human aneuploidy disorders cannot be resolved by radical treatment. However, recent studies have demonstrated that aneuploidies can be rescued to a normal diploid state using genetic engineering in cultured cells. Here, we summarize a series of studies mainly applying genome editing to eliminate an extra copy of human chromosome 21, the cause of the most common constitutional aneuploidy disorder Down syndrome. We also present findings on induced pluripotent stem cell reprogramming, which has been shown to be one of the most promising technologies for converting aneuploidies into normal diploidy without the risk of genetic alterations such as genome editing-mediated off-target effects.
生殖细胞和早期胚胎发育中的染色体分离错误是导致非整倍体的基础,非整倍体是指染色体数目异常,可导致胎儿吸收、发育异常和致癌。人们认为,人类的非整倍体疾病不能通过根治性治疗来解决。然而,最近的研究表明,在培养细胞中使用基因工程可以将非整倍体恢复到正常的二倍体状态。在这里,我们总结了一系列主要应用基因组编辑来消除人类 21 号染色体额外拷贝的研究,21 号染色体是最常见的结构非整倍体疾病唐氏综合征的病因。我们还介绍了诱导多能干细胞重编程的发现,该技术已被证明是将非整倍体转化为正常二倍体的最有前途的技术之一,而不会产生基因组编辑介导的脱靶效应等遗传改变的风险。