Istituto Sperimentale Italiano Lazzaro Spallanzani, Loc. La Quercia, 26027 Rivolta d'Adda (CR), Italy.
Anim Reprod Sci. 2013 Sep;141(1-2):26-33. doi: 10.1016/j.anireprosci.2013.07.003. Epub 2013 Jul 17.
The aim of this study was to establish whether perturbed gene expression during cumulus oocyte development causes repeat breeding in cattle. In this study, a repeat breeder was defined as a normal estrous cycling animal that did not become pregnant after three inseminations despite the absence of clinically detectable reproductive disorders. Transcripts of genes extracted from cumulus oocyte complexes (COC) that were collected from three repeat breeder and three normally fertile Holstein Friesian heifers were compared. Up to 40 COC were collected from each heifer by means of repeated sessions of ovum pick up in the absence of hormonal stimulation; immediately plunged into liquid nitrogen; and stored at -80°C until analysis. For each heifer, RNA was extracted from the pooled COC and hybridized on GeneChip(®) Bovine Gene Array (Affymetrix). Analysis of gene expression profiles of repeat breeder and control COC showed that 178 genes were differentially expressed (log2 fold change>1.5). Of these genes, 43 (24%) were up-regulated and 135 (76%) were down-regulated in repeat breeder relative to control heifers. This altered pattern of expression occurred in genes involved in several cellular biological processes and cellular components such as metabolism, angiogenesis, substrate/ion transport, regulation/signaling, cell adhesion and cytoskeleton. From these, 13 genes potentially involved in cumulus oocyte growth were subjected to validation by qRT-PCR and nine genes (annexin A1, ANXA1; lactoferrin, LTF; interferon stimulated exonuclease 20kDa, ISG20/HEM45; oxidized low density lipoprotein receptor 1, OLR1; fatty acid desaturase 2, FADS2; glutathione S-transferase A2 and A4, GSTA2 and GSTA4; glutathione peroxidase 1, GPX1; endothelin receptor type A, EDNRA) were confirmed to be differentially expressed. This study identified potential marker genes for fertility in dairy cattle.
本研究旨在确定卵丘卵母细胞发育过程中基因表达的改变是否导致奶牛的重复配种。在本研究中,重复配种被定义为正常发情周期的动物,尽管没有临床可检测到的生殖障碍,但在三次授精后仍未怀孕。从 3 头重复配种的牛和 3 头正常产奶荷斯坦弗里生牛的卵丘卵母细胞复合体(COC)中提取的基因转录本进行了比较。通过在没有激素刺激的情况下多次进行卵母细胞采集,从每头奶牛中收集多达 40 个 COC;立即浸入液氮中;并在-80°C 下储存直至分析。对于每头奶牛,从混合的 COC 中提取 RNA,并在 GeneChip®牛基因芯片(Affymetrix)上进行杂交。重复配种和对照 COC 的基因表达谱分析表明,有 178 个基因表达差异(log2 倍数变化>1.5)。在这些基因中,与对照奶牛相比,在重复配种牛中有 43(24%)个基因上调,135(76%)个基因下调。这种表达模式的改变发生在参与几个细胞生物学过程和细胞成分的基因中,如代谢、血管生成、底物/离子转运、调节/信号、细胞黏附和细胞骨架。其中,有 13 个可能参与卵丘卵母细胞生长的基因通过 qRT-PCR 进行了验证,有 9 个基因(膜联蛋白 A1、ANXA1;乳铁蛋白、LTF;干扰素刺激的外切核酸酶 20kDa、ISG20/HEM45;氧化型低密度脂蛋白受体 1、OLR1;脂肪酸去饱和酶 2、FADS2;谷胱甘肽 S-转移酶 A2 和 A4、GSTA2 和 GSTA4;谷胱甘肽过氧化物酶 1、GPX1;内皮素受体 A 型、EDNRA)被证实表达差异。本研究鉴定了奶牛生育能力的潜在标记基因。