Chastant-Maillard S, Campion E, Renard J P
Ecole nationale vétérinaire d'Alfort, Maisons-Alfort, France.
Gynecol Obstet Fertil. 2000 Sep;28(9):649-58.
In mammals, nuclear transfer (or cloning) consists of introducing the nucleus which is generally transcriptionally active into a new cytoplasmic environment, usually that of a transcriptionally inactive metaphase II oocyte. Following the transfer, intense nucleocytoplasmic exchange takes place, and is responsible for remodeling of the nuclear structure and gene reprogramming. The original development program of the donor nucleus is effaced, and the reconstructed embryo adopts that of the recipient oocyte. Both remodeling and reprogramming are regulated by maternal cytoplasmic factors. Overall transcriptional activity, splicing and translational functions as well as the specific expression of certain genes are fairly similar to corresponding activity in normal embryos. However, the development program seems to be read some hours in advance by the reconstructed embryos, and some basic information is lacking. It is particularly important to study these reprogramming abnormalities during the early stages of development in the context of specific abnormalities in fetal and neonatal development observed after transfer of somatic cells.
在哺乳动物中,核移植(或克隆)包括将通常具有转录活性的细胞核导入一个新的细胞质环境中,通常是导入处于转录非活性状态的中期II卵母细胞的细胞质环境。移植后,会发生强烈的核质交换,这负责核结构的重塑和基因重编程。供体细胞核原来的发育程序被抹去,重建后的胚胎采用受体卵母细胞的发育程序。重塑和重编程均受母体细胞质因子调控。总体转录活性、剪接和翻译功能以及某些基因的特异性表达与正常胚胎中的相应活性相当相似。然而,重建后的胚胎似乎会提前几个小时读取发育程序,并且缺乏一些基本信息。在体细胞移植后观察到的胎儿和新生儿发育的特定异常情况下,研究发育早期阶段的这些重编程异常尤为重要。