CHU Montpellier, Institute for Research in Biotherapy, Hôpital Saint-Eloi, INSERM U847, Montpellier, France.
Hum Reprod Update. 2011 Mar-Apr;17(2):272-90. doi: 10.1093/humupd/dmq036. Epub 2010 Aug 17.
The first week of human embryonic development comprises a series of events that change highly specialized germ cells into undifferentiated human embryonic stem cells (hESCs) that display an extraordinarily broad developmental potential. The understanding of these events is crucial to the improvement of the success rate of in vitro fertilization. With the emergence of new technologies such as Omics, the gene expression profiling of human oocytes, embryos and hESCs has been performed and generated a flood of data related to the molecular signature of early embryo development.
In order to understand the complex genetic network that controls the first week of embryo development, we performed a systematic review and study of this issue. We performed a literature search using PubMed and EMBASE to identify all relevant studies published as original articles in English up to March 2010 (n = 165). We also analyzed the transcriptome of human oocytes, embryos and hESCs.
Distinct sets of genes were revealed by comparing the expression profiles of oocytes, embryos on Day 3 and hESCs, which are associated with totipotency, pluripotency and reprogramming properties, respectively. Known components of two signaling pathways (WNT and transforming growth factor-β) were linked to oocyte maturation and early embryonic development.
Omics analysis provides tools for understanding the molecular mechanisms and signaling pathways controlling early embryonic development. Furthermore, we discuss the clinical relevance of using a non-invasive molecular approach to embryo selection for the single-embryo transfer program.
人类胚胎发育的第一周包含一系列事件,这些事件将高度特化的生殖细胞转变为未分化的人类胚胎干细胞(hESCs),后者表现出极其广泛的发育潜能。理解这些事件对于提高体外受精的成功率至关重要。随着新技术(如组学)的出现,对人类卵母细胞、胚胎和 hESC 的基因表达谱进行了分析,并产生了大量与早期胚胎发育分子特征相关的数据。
为了了解控制胚胎发育第一周的复杂遗传网络,我们对这一问题进行了系统的综述和研究。我们使用 PubMed 和 EMBASE 进行了文献检索,以确定截至 2010 年 3 月以英文发表的所有相关研究(n = 165)。我们还分析了人类卵母细胞、胚胎和 hESC 的转录组。
通过比较卵母细胞、第 3 天胚胎和 hESC 的表达谱,揭示了不同的基因集,这些基因集分别与全能性、多能性和重编程特性相关。两个信号通路(WNT 和转化生长因子-β)的已知成分与卵母细胞成熟和早期胚胎发育有关。
组学分析为理解控制早期胚胎发育的分子机制和信号通路提供了工具。此外,我们还讨论了使用非侵入性分子方法进行胚胎选择以用于单胚胎移植计划的临床相关性。