School of Veterinary Medicine, Federal University of Rio Grande do Sul (UFRGS), Porto Alegre, Brazil.
PUCRS, Brazil.
Reprod Domest Anim. 2021 Jun;56(6):857-863. doi: 10.1111/rda.13925. Epub 2021 Mar 25.
The bovine IGF2 locus is a genomic region with alternative transcripts controlled by five promoters (P0, P1, P2, P3 and P4). As transcriptional regulation can affect messenger RNA (mRNA) stability and translation, and thus, subsequent biological effects, this study evaluated the bovine IGF2 promoter-specific expression patterns in oocytes and pre-implantation embryos produced in vitro by our standard IVP procedures. Immature and matured oocytes, and pre-implantation embryos at the 1-, 2-, 4-, 8- and 16-cell, and at early morula, compact morula, blastocyst and expanded blastocyst stages were collected in three pools of five structures per stage, in four replicates. Total RNA was extracted and subjected to RT-qPCR, using four sets of IGF2 promoter-specific primers covering transcripts driven by promoters P0/P1, P2, P3 and P4, with fragments sequenced for confirmation. Expression of P2- and P4-derived transcripts showed an initial peak between immature (P4) or matured (P2/P4) oocytes and 2-cell embryos, gradually falling until embryo genome activation (EGA), rising again at compaction and cavitation. P0/P1-derived transcripts were identified after EGA, during compaction, whereas P3 activity was not detected at any stage. Our findings suggest that P0/P1 and P2 likely have secondary roles during early stages, whereas P3 may be more relevant later in development. P4 seems to be the main pathway for bovine IGF2 expression during oocyte maturation and embryo development and, therefore, the main target to influence IVP in modulation of embryo growth and in studies in developmental biology.
牛 IGF2 基因座是一个具有 5 个启动子(P0、P1、P2、P3 和 P4)控制的替代转录本的基因组区域。由于转录调控可以影响信使 RNA(mRNA)的稳定性和翻译,从而影响随后的生物学效应,因此本研究评估了牛 IGF2 启动子在体外产生的卵母细胞和胚胎中的特异性表达模式。本研究通过我们的标准 IVP 程序,收集了未成熟和成熟卵母细胞,以及处于 1、2、4、8 和 16 细胞阶段以及早期桑葚胚、致密桑葚胚、囊胚和扩张囊胚阶段的前胚胎,每个阶段每 5 个结构为一组,共收集 4 个重复。提取总 RNA,并进行 RT-qPCR,使用四组 IGF2 启动子特异性引物,覆盖由 P0/P1、P2、P3 和 P4 启动子驱动的转录物,并用片段测序进行确认。P2 和 P4 衍生转录物的表达在未成熟(P4)或成熟(P2/P4)卵母细胞和 2 细胞胚胎之间出现初始峰值,逐渐下降至胚胎基因组激活(EGA),在致密化和囊胚腔化时再次上升。P0/P1 衍生的转录物在 EGA 后,在致密化过程中被鉴定出来,而 P3 的活性在任何阶段都没有检测到。我们的研究结果表明,P0/P1 和 P2 在早期阶段可能具有次要作用,而 P3 可能在发育后期更为重要。P4 似乎是牛 IGF2 表达的主要途径,在卵母细胞成熟和胚胎发育过程中,因此是影响 IVP 以调节胚胎生长和在发育生物学研究中的主要靶标。