Ioannidis Jason, Donadeu F Xavier
The Roslin Institute and R(D)SVS, University of Edinburgh, Easter Bush, Midlothian, EH25 9RG, Scotland, UK.
BMC Genomics. 2016 Mar 3;17:184. doi: 10.1186/s12864-016-2529-1.
Low fertility remains a leading cause of poor productivity in dairy cattle. In this context, there is significant interest in developing novel tools for accurate early diagnosis of pregnancy. MicroRNAs (miRNAs) are short RNA molecules which are critically involved in regulating gene expression during both health and disease. MiRNAs have been shown to regulate ovarian function, uterine receptivity, embryonic development and placental function. Circulating miRNAs can provide useful biomarkers of tissue function and disease; importantly, differential miRNA profiles have been linked to pregnancy and preeclampsia in humans. This study sought to establish the potential of circulating miRNAs as biomarkers of early pregnancy in cattle.
We applied Illumina small-RNA sequencing to profile miRNAs in plasma samples collected from eight non-pregnant heifers on Days 0, 8 and 16 of the oestrous cycle and 11 heifers on Days 16 and 24 of pregnancy. We sequenced a total of 46 samples and generated 9.2 million miRNA reads per sample. There were no differences in miRNA read abundance between any of the pregnant and non-pregnant time-points (FDR > 0.1). As a complementary approach, we analysed sample pools (3-4 samples/pool) corresponding to Days 0, 8 and 16 of the oestrous cycle and Day 24 of pregnancy (n = 3 pools/group) using Qiagen PCR arrays. A total of 16 miRNAs were differentially expressed (FDR < 0.1) in plasma between pregnant and non-pregnant animals. RT-qPCR validation using the same plasma samples confirmed that miR-26a was differentially upregulated on Day 16 pregnant relative to non-pregnant heifers (1.7-fold; P = 0.043), whereas miR-1249 tended to be upregulated in Day 16 pregnant heifers (1.6-fold; P = 0.081). Further validation in an independent group of heifers confirmed an increase in plasma miR-26a levels during early pregnancy, which was significant only on Day 24 (2.0-fold; P = 0.027).
Through genome-wide analyses we have successfully profiled plasma miRNA populations associated with early pregnancy in cattle. We have identified miR-26a as a potential circulating biomarker of early pregnancy.
低生育力仍然是奶牛生产力低下的主要原因。在此背景下,人们对开发用于准确早期诊断妊娠的新型工具有着浓厚兴趣。微小RNA(miRNA)是短RNA分子,在健康和疾病过程中都关键地参与调节基因表达。已表明miRNA可调节卵巢功能、子宫容受性、胚胎发育和胎盘功能。循环miRNA可提供组织功能和疾病的有用生物标志物;重要的是,不同的miRNA谱已与人类的妊娠和先兆子痫相关联。本研究旨在确定循环miRNA作为牛早期妊娠生物标志物的潜力。
我们应用Illumina小RNA测序对从8头未怀孕小母牛在发情周期的第0、8和16天以及11头怀孕小母牛在妊娠第16和24天采集的血浆样本中的miRNA进行分析。我们总共对46个样本进行了测序,每个样本产生了920万个miRNA读数。在任何怀孕和未怀孕时间点之间,miRNA读数丰度均无差异(FDR>0.1)。作为一种补充方法,我们使用Qiagen PCR阵列分析了与发情周期的第0、8和16天以及妊娠第24天相对应的样本池(3 - 4个样本/池)(每组n = 3个样本池)。共有16种miRNA在怀孕和未怀孕动物的血浆中差异表达(FDR<0.1)。使用相同血浆样本进行的RT - qPCR验证证实,与未怀孕小母牛相比,怀孕第16天的小母牛血浆中miR - 26a差异上调(1.7倍;P = 0.043),而miR - 1249在怀孕第16天的小母牛中倾向于上调(1.6倍;P = 0.081)。在另一组独立的小母牛中进一步验证证实,妊娠早期血浆miR - 26a水平升高,仅在第24天显著(2.0倍;P = 0.027)。
通过全基因组分析,我们成功分析了与牛早期妊娠相关的血浆miRNA群体。我们已确定miR - 26a为早期妊娠的潜在循环生物标志物。