microRNA Profiling of Amniotic Fluid: Evidence of Synergy of microRNAs in Fetal Development.

Amniotic fluid (AF) continuously exchanges molecules with the fetus, playing critical roles in fetal development especially via its complex components. Among these components, microRNAs are thought to be transferred between cells loaded in microvesicles. However, the functions of AF microRNAs remain...

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Main Authors: Tingting Sun, Weiyun Li, Tianpeng Li, Shucai Ling
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4864075?pdf=render
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spelling doaj-8bce3dac9cdb4534a6c56f1d073303702020-11-25T02:31:45ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01115e015395010.1371/journal.pone.0153950microRNA Profiling of Amniotic Fluid: Evidence of Synergy of microRNAs in Fetal Development.Tingting SunWeiyun LiTianpeng LiShucai LingAmniotic fluid (AF) continuously exchanges molecules with the fetus, playing critical roles in fetal development especially via its complex components. Among these components, microRNAs are thought to be transferred between cells loaded in microvesicles. However, the functions of AF microRNAs remain unknown. To date, few studies have examined microRNAs in amniotic fluid. In this study, we employed miRCURY Locked Nucleotide Acid arrays to profile the dynamic expression of microRNAs in AF from mice on embryonic days E13, E15, and E17. At these times, 233 microRNAs were differentially expressed (p< 0.01), accounting for 23% of the total Mus musculus microRNAs. These differentially-expressed microRNAs were divided into two distinct groups based on their expression patterns. Gene ontology analysis showed that the intersectional target genes of these differentially-expressed microRNAs were mainly distributed in synapse, synaptosome, cell projection, and cytoskeleton. Pathway analysis revealed that the target genes of the two groups of microRNAs were synergistically enriched in axon guidance, focal adhesion, and MAPK signaling pathways. MicroRNA-mRNA network analysis and gene- mapping showed that these microRNAs synergistically regulated cell motility, cell proliferation and differentiation, and especially the axon guidance process. Cancer pathways associated with growth and proliferation were also enriched in AF. Taken together, the results of this study are the first to show the functions of microRNAs in AF during fetal development, providing novel insights into interpreting the roles of AF microRNAs in fetal development.http://europepmc.org/articles/PMC4864075?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Tingting Sun
Weiyun Li
Tianpeng Li
Shucai Ling
spellingShingle Tingting Sun
Weiyun Li
Tianpeng Li
Shucai Ling
microRNA Profiling of Amniotic Fluid: Evidence of Synergy of microRNAs in Fetal Development.
PLoS ONE
author_facet Tingting Sun
Weiyun Li
Tianpeng Li
Shucai Ling
author_sort Tingting Sun
title microRNA Profiling of Amniotic Fluid: Evidence of Synergy of microRNAs in Fetal Development.
title_short microRNA Profiling of Amniotic Fluid: Evidence of Synergy of microRNAs in Fetal Development.
title_full microRNA Profiling of Amniotic Fluid: Evidence of Synergy of microRNAs in Fetal Development.
title_fullStr microRNA Profiling of Amniotic Fluid: Evidence of Synergy of microRNAs in Fetal Development.
title_full_unstemmed microRNA Profiling of Amniotic Fluid: Evidence of Synergy of microRNAs in Fetal Development.
title_sort microrna profiling of amniotic fluid: evidence of synergy of micrornas in fetal development.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2016-01-01
description Amniotic fluid (AF) continuously exchanges molecules with the fetus, playing critical roles in fetal development especially via its complex components. Among these components, microRNAs are thought to be transferred between cells loaded in microvesicles. However, the functions of AF microRNAs remain unknown. To date, few studies have examined microRNAs in amniotic fluid. In this study, we employed miRCURY Locked Nucleotide Acid arrays to profile the dynamic expression of microRNAs in AF from mice on embryonic days E13, E15, and E17. At these times, 233 microRNAs were differentially expressed (p< 0.01), accounting for 23% of the total Mus musculus microRNAs. These differentially-expressed microRNAs were divided into two distinct groups based on their expression patterns. Gene ontology analysis showed that the intersectional target genes of these differentially-expressed microRNAs were mainly distributed in synapse, synaptosome, cell projection, and cytoskeleton. Pathway analysis revealed that the target genes of the two groups of microRNAs were synergistically enriched in axon guidance, focal adhesion, and MAPK signaling pathways. MicroRNA-mRNA network analysis and gene- mapping showed that these microRNAs synergistically regulated cell motility, cell proliferation and differentiation, and especially the axon guidance process. Cancer pathways associated with growth and proliferation were also enriched in AF. Taken together, the results of this study are the first to show the functions of microRNAs in AF during fetal development, providing novel insights into interpreting the roles of AF microRNAs in fetal development.
url http://europepmc.org/articles/PMC4864075?pdf=render
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