Département des Sciences Animales, Faculté des sciences de l'agriculture et de l'alimentation, Centre de Recherche en Biologie de la Reproduction, INAF, Université Laval, Québec, Québec, Canada.
Reproduction. 2011 Jul;142(1):99-112. doi: 10.1530/REP-10-0477. Epub 2011 Apr 12.
In vitro production (IVP) of cattle embryos over the past two decades has revealed several negative impacts that have been attributed to the artificial microenvironment. Studies on embryos produced in vitro clearly point to aberrant gene expression levels. So far, the causal association between phenotype and measured gene expression has not led to substantial improvement of IVP systems. The aim of this study was to generate a unique dataset composed of microarray-derived relative transcript abundance values for blastocysts produced in ten in vitro systems differing primarily in culture medium formulation. Between-group comparisons determine the level of overall similarity among systems relative to in vivo reference embryos. The use of the dataset to contrast all in vitro treatments with the in vivo blastocysts pointed to a single common gene network. The 'boutique' array contained a panel of novel uncharacterized transcripts that were variably expressed depending on the medium in which the blastocysts were produced. These novel transcripts were differentially expressed in blastocysts even as carryover from conditions encountered 7 days earlier during oocyte maturation. All of the selected novel candidates thus expressed were from intergenic regions. The function of this long non-coding RNA remains unknown but clearly points to an additional level of complexity in early embryo development.
在过去的二十年中,牛胚胎的体外生产(IVP)揭示了一些被归因于人工微环境的负面影响。关于体外生产胚胎的研究清楚地指出了异常的基因表达水平。到目前为止,表型和测量的基因表达之间的因果关系尚未导致 IVP 系统的实质性改进。本研究的目的是生成一个独特的数据集,该数据集由在十种主要在培养基配方上有所不同的体外系统中生产的囊胚的微阵列衍生的相对转录丰度值组成。组间比较确定了系统之间相对于体内参考胚胎的整体相似性水平。使用该数据集将所有体外处理与体内囊胚进行对比,指出了一个单一的共同基因网络。“精品”阵列包含一组新的未表征的转录本,这些转录本的表达根据囊胚产生的培养基而变化。即使在卵母细胞成熟过程中 7 天前遇到的条件有残留,这些新型转录本在囊胚中也表现出差异表达。因此,所有选定的新型候选者都来自基因间区域。这种长非编码 RNA 的功能尚不清楚,但显然表明早期胚胎发育具有额外的复杂性。