Abstract

MicroRNAs (miRNAs) are a class of small RNA molecules that regulate gene expression by inhibiting the protein translation or targeting the mRNA cleavage. They play many important roles in living organism cells; however, the knowledge on miRNAs functions has become more extensive upon their identification in biological fluids and recent reports on plant-origin miRNAs abundance in human plasma and serum. Considering these findings, we performed a rigorous bioinformatics analysis of publicly available, raw data from high-throughput sequencing studies on miRNAs composition in human and porcine breast milk exosomes to identify the fraction of food-derived miRNAs. Several processing and filtering steps were applied to increase the accuracy, and to avoid false positives. Through aforementioned analysis, 35 and 17 miRNA species, belonging to 25 and 11 MIR families, were identified, respectively. In the human samples the highest abundance levels yielded the ath-miR166a, pab-miR951, ptc-miR472a and bdi-miR168, while in the porcine breast milk exosomes, the zma-miR168a, zma-miR156a and ath-miR166a have been identified in the largest amounts. The consensus prediction and annotation of potential human targets for select plant miRNAs suggest that the aforementioned molecules may interact with mRNAs coding several transcription factors, protein receptors, transporters and immune-related proteins, thus potentially influencing human organism. Taken together, the presented analysis shows proof of abundant plant miRNAs in mammal breast milk exosomes, pointing at the same time to the new possibilities arising from this discovery.

Highlights

  • MicroRNAs are a class of short (18–24 nt) regulatory RNAs that are widely evolutionary conserved among many species [1,2]

  • The raw data collected from 8 porcine and 4 human small RNA libraries included over 179.90 and 86.37 million reads, respectively

  • For a second verification step, the reduced collections of potential exogenous miRNAs sequences from S. scrofa and H. sapiens were mapped to the pig and human genomes, respectively

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Summary

Introduction

MicroRNAs (miRNAs) are a class of short (18–24 nt) regulatory RNAs that are widely evolutionary conserved among many species [1,2] These single-stranded, non-coding molecules mediate posttranscriptional gene regulation by promoting cleavage or inhibiting translation of the target mRNA [3,4]. The second strand is loaded on the RISC (RNA-Induced Silencing Complex) multi-complex and binds to the specific mRNA transcript [6]. Throughout this hybridization, miRNAs negatively regulate expression of target genes, which control cell development, apoptosis, proliferation, differentiation and function in living organisms [7,8]. In medicine, miRNAs have become new diagnostic and prognostic biomarkers [11,12], and have been incorporated in a few therapies for treating several human disorders [13,14]

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