Krawczynski Kamil, Bauersachs Stefan, Reliszko Zaneta P, Graf Alexander, Kaczmarek Monika M
Institute of Animal Reproduction and Food Research Polish Academy of Sciences (IARFR PAS), Tuwima 10, 10-748, Olsztyn, Poland.
Laboratory for Functional Genome Analysis (LAFUGA), LMU University of Munich, Feodor-Lynen-Strasse 25, Munich, 81377, Germany.
BMC Genomics. 2015 Nov 6;16:906. doi: 10.1186/s12864-015-2172-2.
Embryo implantation is a complex, synchronized process that requires establishment of a reciprocal dialogue between a receptive endometrium and developing blastocysts. Recently, microRNAs (miRNAs), known to modulate gene expression through post-transcriptional mechanisms, were implicated in regulation of early pregnancy events including maternal recognition of pregnancy and implantation. To characterize complex transcriptomic changes, expression of miRNAs in pregnant and cyclic endometria collected on days 12, 16 and 20 was analyzed using Illumina deep sequencing and analyzed with bioinformatic pipeline. Moreover, expression profiles of ten genes related to miRNA synthesis and transport such as DROSHA, DGCR8, XPO5, DICER, TARBP2, TNRC6A, and AGO1-4 were determined.
Among genes involved in miRNA transport and synthesis DROSHA, XPO5, DICER1, TARBP, and AGO1 expression was affected by the reproductive status. Moreover, DICER1 and AGO2 proteins were localized in luminal and glandular epithelium with immunofluorescence staining. Several hundred mature, canonical and non-canonical miRNAs were found to be expressed in the endometrial samples. Detailed analysis revealed that miRNA length variants, isomiRs, accounted for the vast majority of defined sequences. Both miRNA and isomiR of miR-140-3p were shown to affect expression of putative targets in endometrial stromal cells in vitro. Computational analysis of putative target genes for miRNAs differentially expressed (DE) between pregnant and cyclic animals resulted in lists of biological processes and regulatory pathways indicating their role in cellular development, cell cycle, immunological response and organismal development. Among predicted target genes for DE miRNAs, vascular endothelial growth factor (VEGF), progesterone and estradiol receptors (PGR, ESR1) and leukemia inhibitory factor (LIF) were found.
This research revealed a repertoire of pregnancy-related miRNAs in porcine endometrium during initial stages of conceptus implantation and during the estrous cycle, and sheds light on mechanisms regulating miRNA-mediated gene expression at the maternal-conceptus interface.
胚胎着床是一个复杂的同步过程,需要在接受性子宫内膜和发育中的囊胚之间建立相互对话。最近,已知通过转录后机制调节基因表达的微小RNA(miRNA)参与了早期妊娠事件的调节,包括母体对妊娠的识别和着床。为了表征复杂的转录组变化,使用Illumina深度测序分析了在第12、16和20天收集的妊娠和周期性子宫内膜中miRNA的表达,并通过生物信息学管道进行分析。此外,还确定了与miRNA合成和转运相关的十个基因(如DROSHA、DGCR8、XPO5、DICER、TARBP2、TNRC6A和AGO1 - 4)的表达谱。
在参与miRNA转运和合成的基因中,DROSHA、XPO5、DICER1、TARBP和AGO1的表达受生殖状态影响。此外,通过免疫荧光染色发现DICER1和AGO2蛋白定位于腔上皮和腺上皮。在子宫内膜样本中发现数百种成熟的、典型的和非典型的miRNA表达。详细分析表明,miRNA长度变体(异源miR)占已定义序列的绝大多数。miR - 140 - 3p的miRNA和异源miR均显示在体外影响子宫内膜基质细胞中假定靶标的表达。对妊娠和周期性动物之间差异表达(DE)的miRNA的假定靶基因进行计算分析,得出了生物过程和调节途径列表,表明它们在细胞发育、细胞周期、免疫反应和机体发育中的作用。在DE miRNA的预测靶基因中,发现了血管内皮生长因子(VEGF)、孕酮和雌激素受体(PGR、ESR1)以及白血病抑制因子(LIF)。
本研究揭示了猪子宫内膜在胚胎着床初始阶段和发情周期中与妊娠相关的miRNA库,并阐明了在母体 - 胚胎界面调节miRNA介导的基因表达的机制。