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microRNAs in Macrobrachium olfersii embryos: Identification, their biogenesis components and potential targets

  • Michael L. Jaramillo
    ,
  • ,
  • Guilherme C. da Fonseca
    ,
  • Rogerio Margis
    ,
  • Yara M.R. Müller
    ,
  • Dib Ammar
*Corresponding author for this work
  • Federal University of Santa Catarina-UFSC
    ,
  • Federal University of Rio Grande do Sul
    ,
  • Centro Universitário – Católica de Santa Catarina
Research Output:
Contribution to journal
Article
Peer-review

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 205-216 (12 pages)

Journal (Volume, Issue Number)

Computational Biology and Chemistry (Volume 78)

Publication milestones

  • Published - 02/2019

Publication status

Published - 02/2019

ISSN

1476-9271

Publication IDs

  • Scopus: 85058511409
  • PubMed: 30576966

Abstract

In embryonic development, microRNAs (miRNAs) regulate the complex gene expression associated with the complexity of embryogenesis. Today, few studies have been conducted on the identification of miRNAs and components of miRNA biogenesis on embryonic development in crustaceans, especially in prawns. In this context, the aim of this study was to identify in silico components of miRNA biogenesis, and miRNAs and potential target genes during embryonic development in the prawn Macrobrachium olfersii through small RNAs and transcriptome analyses. Using the miRDeep2 program, we identified 17 miRNA precursors in M. olfersii, which seven (miR-9, miR-10, miR-92, miR-125, miR-305, miR-1175, and miR-2788) were reported in the miRBase database, indicating high evolutionary conservation of these sequences among animals. The other 10 miRNAs of M. olfersii were novel miRNAs and only similar to Macrobrachium niponnense miRNAs, indicating genus-specific miRNAs. In addition, eight key components of miRNA biogenesis (DROSHA, PASHA/DGCR8, XPO5, RAN, DICER, TRBP2, AGO, and PIWI) were identified in M. olfersii embryos unigenes. In the annotation of miRNA targets, 516 genes were similar to known sequences in the GenBank database. Regarding the conserved miRNAs, we verified that they were differentially expressed during embryonic development in M. olfersii. In conclusion, this is the first study that identifies conserved and novel miRNAs in the prawn M. olfersii with some miRNA target genes involved in embryonic development. Our results will allow further studies on the function of these miRNAs and miRNA biogenesis components during embryonic development in M. olfersii and other prawns of commercial interest.