Wakamatsu Yuko
Laboratory of Freshwater Fish Stocks, Bioscience and Biotechnology Center, Nagoya University, Furo-cho, Nagoya, Japan.
Dev Growth Differ. 2008 Aug;50(6):427-36. doi: 10.1111/j.1440-169X.2008.01050.x.
Until recently, the nuclear transfer of adult somatic cell nuclei in fish has been unsuccessful. This is primarily because of chromosomal aberrations in nuclear transplants, which are thought to arise due to asynchrony between the cell cycles of the recipient egg and donor nucleus. We recently succeeded in circumventing this difficulty by using a new nuclear transfer method in medaka fish (Oryzias latipes). Instead of enucleated eggs, the method uses non-enucleated and diploidized eggs, obtained by retention of the second polar body release, as recipients in the nuclear transfer of primary culture cells from the caudal fin of an adult green fluorescent protein gene (GFP)-transgenic strain. We found that 2.7% of the reconstructed embryos grew into diploid and fertile adults exhibiting donor expression characteristics and transmission of the GFP marker gene to progeny. The mechanism underlying the generation of nuclear transplants using this method is unknown at present; however, analyses of donor and recipient nuclei behavior and the cytoskeletal mechanisms involved in the early developmental stages, as well as the special ability of diploidized eggs to facilitate reprogramming of the donor nuclei will result in elucidation of the mechanism.
直到最近,鱼类成年体细胞的核移植一直未成功。这主要是由于核移植中的染色体畸变,据认为这是由于受体卵和供体细胞核的细胞周期不同步所致。我们最近通过在青鳉鱼(Oryzias latipes)中使用一种新的核移植方法成功克服了这一困难。该方法不是使用去核卵,而是使用通过保留第二极体释放而获得的未去核且二倍体化的卵,作为来自成年绿色荧光蛋白基因(GFP)转基因品系尾鳍的原代培养细胞进行核移植的受体。我们发现,2.7%的重构胚胎发育成了具有供体表达特征且能将GFP标记基因传递给后代的二倍体可育成体。目前尚不清楚使用该方法产生核移植体的潜在机制;然而,对供体和受体细胞核行为以及早期发育阶段所涉及的细胞骨架机制的分析,以及二倍体化卵促进供体细胞核重编程的特殊能力,将有助于阐明该机制。