Large-scale transcriptional analysis of bovine embryo biopsies in relation to pregnancy success after transfer to recipients

被引:201
作者
El-Sayed, Ashraf
Hoelker, Michael
Rings, Franca
Salilew, Dessie
Jennen, Danyel
Tholen, Ernst
Sirard, Marc-Andre
Schellander, Karl
Tesfaye, Dawit
机构
[1] Univ Bonn, Inst Anim Sci, Anim Breeding & Husb Grp, Bonn, Germany
[2] Univ Laval, Dept Anim Sci, Ctr Rech Biol Reprod, Ste Foy, PQ G1K 7P4, Canada
关键词
blastocyst; preimplantation; embryo loss; microarray;
D O I
10.1152/physiolgenomics.00111.2006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The purpose of this work is to address the relationship between transcriptional profile of embryos and the pregnancy success based on gene expression analysis of blastocyst biopsies taken prior to transfer to recipients. Biopsies (30-40% of the intact embryo) were taken from in vitro-produced day 7 blastocysts (n = 118), and 60 - 70% were transferred to recipients after reexpansion. Based on the success of pregnancy, biopsies were pooled in three groups (each 10 biopsies) namely: those resulting in no pregnancy (G1), resorbed embryos (G2), and those resulting in calf delivery (G3). Gene expression analysis of these groups was performed using home-made bovine preimplantation-specific cDNA array (219 clones) and BlueChip (with similar to 2,000 clones). Microarray data analysis results revealed a total of 52 and 58 genes were differentially regulated during comparison between G1 vs. G3 and G2 vs. G3. Biopsies resulted in calf delivery were enriched with genes necessary for implantation (COX2 and CDX2), carbohydrate metabolism (ALOX15), growth factor (BMP15), signal transduction (PLAU), and placenta-specific 8 (PLAC8). Biopsies from embryos resulting in resorption are enriched with transcripts involved protein phosphorylation (KRT8), plasma membrane (OCLN), and glucose metabolism (PGK1 and AKR1B1). Biopsies from embryos resulting in no pregnancy are enriched with transcripts involved inflammatory cytokines (TNF), protein amino acid binding (EEF1A1), transcription factors (MSX1, PTTG1), glucose metabolism (PGK1, AKR1B1), and CD9, which is an inhibitor of implantation. In conclusion, we generated direct candidates of blastocyst-specific genes which may play an important role in determining the fate of the embryo after transfer.
引用
收藏
页码:84 / 96
页数:13
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