Warner C M, Cao W, Exley G E, McElhinny A S, Alikani M, Cohen J, Scott R T, Brenner C A
Department of Biology, Northeastern University, Boston, MA, USA.
Hum Reprod. 1998 Jun;13 Suppl 3:178-90; discussion 191-6. doi: 10.1093/humrep/13.suppl_3.178.
In both mice and humans, 15-50% of embryos die during the preimplantation period from mechanisms that are largely unknown. Two major criteria predict preimplantation embryo quality, the rate of development and the degree of fragmentation. We review evidence that both of these criteria have a genetic basis. Rate of development and subsequent embryo survival are controlled by a gene, Ped, we discovered in the mouse. Although progress is being made in the search for the human homologue of the mouse Ped gene, it has not yet been identified. Fragmentation, observed in both mouse and human embryos, is probably the result of apoptosis. We analysed transcription of two genes that regulate apoptosis, bcl-2 and bax, and found that both are transcribed in mouse and human preimplantation embryos. Overall, the literature reviewed and new data presented in this paper support the concept that there is a genetic basis for preimplantation egg and embryo survival.
在小鼠和人类中,15%至50%的胚胎在着床前期死亡,其机制大多未知。有两个主要标准可预测着床前胚胎质量,即发育速率和碎片化程度。我们综述了证据表明这两个标准都有遗传基础。发育速率及随后的胚胎存活率由我们在小鼠中发现的一个基因Ped控制。尽管在寻找小鼠Ped基因的人类同源物方面取得了进展,但尚未确定。在小鼠和人类胚胎中均观察到的碎片化可能是细胞凋亡的结果。我们分析了两个调节细胞凋亡的基因bcl-2和bax的转录情况,发现它们在小鼠和人类着床前胚胎中均有转录。总体而言,本文综述的文献和新数据支持这样一种概念,即着床前卵子和胚胎存活存在遗传基础。