Human plasma pregnancy-associated miRNAs and their temporal variation within the first trimester of pregnancy.

Cécilia Légaré, Andrée-Anne Clément, Véronique Desgagné, Kathrine Thibeault, Frédérique White, Simon-Pierre Guay, Benoit J Arsenault, Michelle S Scott, Pierre-Étienne Jacques, Patrice Perron, Renée Guérin, Marie-France Hivert, Luigi Bouchard
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引用次数: 12

Abstract

Background: During pregnancy, maternal metabolism undergoes substantial changes to support the developing fetus. Such changes are finely regulated by different mechanisms carried out by effectors such as microRNAs (miRNAs). These small non-coding RNAs regulate numerous biological functions, mostly through post-transcriptional repression of gene expression. miRNAs are also secreted in circulation by numerous organs, such as the placenta. However, the complete plasmatic microtranscriptome of pregnant women has still not been fully described, although some miRNA clusters from the chromosome 14 (C14MC) and the chromosome 19 (C19MC and miR-371-3 cluster) have been proposed as being specific to pregnancy. Our aims were thus to describe the plasma microtranscriptome during the first trimester of pregnancy, by assessing the differences with non-pregnant women, and how it varies between the 4th and the 16th week of pregnancy.

Methods: Plasmatic miRNAs from 436 pregnant (gestational week 4 to 16) and 15 non-pregnant women were quantified using Illumina HiSeq next-generation sequencing platform. Differentially abundant miRNAs were identified using DESeq2 package (FDR q-value ≤ 0.05) and their targeted biological pathways were assessed with DIANA-miRpath.

Results: A total of 2101 miRNAs were detected, of which 191 were differentially abundant (fold change < 0.05 or > 2, FDR q-value ≤ 0.05) between pregnant and non-pregnant women. Of these, 100 miRNAs were less and 91 miRNAs were more abundant in pregnant women. Additionally, the abundance of 57 miRNAs varied according to gestational age at first trimester, of which 47 were positively and 10 were negatively associated with advancing gestational age. miRNAs from the C19MC were positively associated with both pregnancy and gestational age variation during the first trimester. Biological pathway analysis revealed that these 191 (pregnancy-specific) and 57 (gestational age markers) miRNAs targeted genes involved in fatty acid metabolism, ECM-receptor interaction and TGF-beta signaling pathways.

Conclusion: We have identified circulating miRNAs specific to pregnancy and/or that varied with gestational age in first trimester. These miRNAs target biological pathways involved in lipid metabolism as well as placenta and embryo development, suggesting a contribution to the maternal metabolic adaptation to pregnancy and fetal growth.

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人血浆妊娠相关mirna及其妊娠前三个月的时间变化。
背景:在怀孕期间,母亲的新陈代谢经历了实质性的变化,以支持胎儿的发育。这些变化是由诸如microrna (miRNAs)等效应物所执行的不同机制精细调节的。这些小的非编码rna调节许多生物功能,主要是通过转录后基因表达的抑制。许多器官,如胎盘,也会在循环中分泌mirna。然而,尽管已经提出来自14号染色体(C14MC)和19号染色体(C19MC和miR-371-3簇)的一些miRNA簇是妊娠特异性的,但孕妇的完整血浆微转录组仍未得到充分的描述。因此,我们的目的是通过评估与未怀孕妇女的差异,以及妊娠第4周和第16周之间的差异,来描述妊娠前三个月的血浆微转录组。方法:采用Illumina HiSeq新一代测序平台对436例孕妇(孕4 ~孕16周)和15例非孕妇的血浆mirna进行定量分析。采用DESeq2包鉴定差异丰度mirna (FDR q值≤0.05),采用DIANA-miRpath评估其靶向生物学途径。结果:共检测到2101个mirna,其中191个在孕妇和非孕妇中差异丰富(fold change 2, FDR q值≤0.05)。其中,孕妇体内有100种mirna较少,91种mirna较多。此外,57种mirna的丰度随孕早期胎龄的变化而变化,其中47种与孕早期胎龄呈正相关,10种与孕早期胎龄负相关。来自C19MC的mirna与妊娠早期妊娠和胎龄变化呈正相关。生物学通路分析显示,这191个(妊娠特异性)和57个(胎龄标记)mirna靶向的基因参与脂肪酸代谢、ecm受体相互作用和tgf - β信号通路。结论:我们已经确定了妊娠特异性和/或妊娠早期随胎龄变化的循环mirna。这些mirna靶向参与脂质代谢以及胎盘和胚胎发育的生物学途径,表明母体代谢适应妊娠和胎儿生长有贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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