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Genome-wide expression profile of trophoblastic cells during late pregnancy in ewes
Genome-wide expression profile of trophoblastic cells during late pregnancy in ewes
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Genome-wide expression profile of trophoblastic cells during late pregnancy in ewes
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Genome-wide expression profile of trophoblastic cells during late pregnancy in ewes
Genome-wide expression profile of trophoblastic cells during late pregnancy in ewes

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Genome-wide expression profile of trophoblastic cells during late pregnancy in ewes
Genome-wide expression profile of trophoblastic cells during late pregnancy in ewes
Journal Article

Genome-wide expression profile of trophoblastic cells during late pregnancy in ewes

2020
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Overview
During pregnancy, the placenta plays a pivotal role in fetal-maternal communication. Despite the known involvement of trophoblast mononuclear (MNC) and binuclear (BNC) cells in placentation and fetal development, the regulatory mechanisms underlying the gene expression in these cells and their role in pregnancy have not been fully elucidated. Thus, a genome-wide expression profile analysis of MNC and BNC from ovine placentomes on day 90 and 130 of pregnancy was performed to identify differentially expressed genes (DEG) and regulatory pathways. After tissue separation, enzymatic digestion, and elutriation, MNC and BNC were obtained, and the total RNA was isolated and sequenced (n = 2 ewes/day). Differential expression analysis was carried out with DESeq2 after library quality control and read mapping using FastQC and STAR, respectively. Among six pairwise contrasts possible, herein, we focused on the one between MNC and BNC on day 130. Accordingly, we identified 514 genes upregulated and 161 downregulated in BNC (adj.Pval < 0.05). Interestingly, we found nine DE long intergenic noncoding RNAs (lincRNA). Although the function of lincRNAs remains under investigation, its transcription has been associated with gene expression regulation in utero. The DEGs functional over-representation analysis included Rap1 and PI3k-Akt signaling pathways as up-regulated in BNC (adj.Pval. < 0.05). These pathways are activated by extracellular signals and are involved in cell proliferation and differentiation, morphogenesis, and energy metabolism. Furthermore, we identified PLA2G10 gene that codes a phospholipase protein involved in the production of prostaglandins, which have been associated with placental blood flow. These findings suggest an intricate and complex network underlying gene expression between cells and time points that are essential for the fetal-maternal placenta relationship. This project was supported by Agriculture and Food Research Initiative Competitive Grant n. 2016-67016-24884 from the USDA National Institute of Food and Agriculture.