MicroRNA identity and abundance in porcine skeletal muscles determined by deep sequencing:

M Nielsen, J H Hansen, J Hedegaard, R O Nielsen, F Panitz, C Bendixen, B Thomsen

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    Abstract

    MicroRNAs (miRNA) are short single-stranded RNA molecules that regulate gene expression post-transcriptionally by binding to complementary sequences in the 3' untranslated region (3' UTR) of target mRNAs. MiRNAs participate in the regulation of myogenesis, and identification of the complete set of miRNAs expressed in muscles is likely to significantly increase our understanding of muscle growth and development. To determine the identity and abundance of miRNA in porcine skeletal muscle, we applied a deep sequencing approach. This allowed us to identify the sequences and relative expression levels of 212 annotated miRNA genes, thereby providing a thorough account of the miRNA transcriptome in porcine muscle tissue. The expression levels displayed a very large range, as reflected by the number of sequence reads, which varied from single counts for rare miRNAs to several million reads for the most abundant miRNAs. Moreover, we identified numerous examples of mature miRNAs that were derived from opposite sides of the same predicted precursor stem-loop structures, and also observed length and sequence heterogeneity at the 5' and 3' ends. Furthermore, KEGG pathway analysis suggested that highly expressed miRNAs are involved in skeletal muscle development and regeneration, signal transduction, cell-cell and cell-extracellular matrix communication and neural development and function.
    Original languageEnglish
    JournalAnimal Genetics
    Volume41
    Issue2
    Pages (from-to)159-168
    Number of pages10
    ISSN0268-9146
    DOIs
    Publication statusPublished - 2010

    Keywords

    • deep sequencing
    • microRNA
    • skeletal muscles
    • Sus scrofa
    • transcriptome

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