Exploration of Long Non-coding RNAs and Circular RNAs in Porcine Milk Exosomes

Bin Zeng1, Ting Chen1, Junyi Luo1

  • 1Guangdong Provincial Key Laboratory of Animal Nutrition Control, National Engineering Research Center for Breeding Swine Industry, College of Animal Science, South China Agricultural University, Guangzhou, China.

Frontiers in Genetics
|July 28, 2020
PubMed

Insights

Porcine milk exosomes contain novel long non-coding RNAs (lncRNAs) and circular RNAs (circRNAs) that may regulate gene expression. This study identifies these non-coding RNAs and their potential interactions with microRNAs (miRNAs).

Area of Science:

  • Exosomes and extracellular vesicles
  • Non-coding RNA biology
  • Animal reproductive biology

Background:

  • Milk exosomes are known to contain microRNAs (miRNAs) and messenger RNAs (mRNAs) capable of intestinal absorption and gene regulation.
  • Long non-coding RNAs (lncRNAs) and circular RNAs (circRNAs) play crucial roles in animal biological processes, but their presence and function in porcine milk exosomes (PME) remain uncharacterized.

Purpose of the Study:

  • To comprehensively analyze the expression profiles of lncRNAs and circRNAs within porcine milk exosomes (PME).
  • To investigate the potential functions and interactions of these non-coding RNAs with miRNAs in PME.

Main Methods:

  • Isolation of PME via ultracentrifugation.
  • Comprehensive RNA sequencing to identify and characterize lncRNAs and circRNAs in PME.
  • Quantitative PCR (qPCR) for validation of selected lncRNAs and circRNAs.
  • Bioinformatic analysis for functional enrichment and miRNA interaction prediction.

Main Results:

  • Identification of 2,466 novel and 809 annotated lncRNAs, along with 61 circRNAs in PME.
  • lncRNAs in PME exhibited characteristics similar to other mammals but were more abundant than mRNAs.
  • Functional enrichment analysis suggested PME lncRNAs target genes involved in metabolism and immunity, while circRNAs target genes related to nucleic acid binding and cell adhesion.
  • High density of miRNA target sites was observed on PME lncRNAs and circRNAs, with specific interactions linked to proliferation and intestinal barrier functions.

Conclusions:

  • This study provides the first comprehensive resource for lncRNA and circRNA research in porcine milk.
  • Revealed potential interactions between PME lncRNAs/circRNAs and miRNAs, suggesting regulatory roles in gene expression.
  • Expands the understanding of non-coding RNA content in milk, highlighting the need for further research into their physiological functions.

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