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A microRNA-mRNA expression network during oral siphon regeneration in Ciona.
Spina, Elijah J; Guzman, Elmer; Zhou, Hongjun; Kosik, Kenneth S; Smith, William C.
Afiliação
  • Spina EJ; Department of Molecular, Cell and Developmental Biology, University of California, Santa Barbara, Santa Barbara, CA 93106, USA.
  • Guzman E; Department of Molecular, Cell and Developmental Biology, University of California, Santa Barbara, Santa Barbara, CA 93106, USA.
  • Zhou H; Neuroscience Research Institute, University of California, Santa Barbara, Santa Barbara, CA 93106, USA.
  • Kosik KS; Department of Molecular, Cell and Developmental Biology, University of California, Santa Barbara, Santa Barbara, CA 93106, USA.
  • Smith WC; Neuroscience Research Institute, University of California, Santa Barbara, Santa Barbara, CA 93106, USA.
Development ; 144(10): 1787-1797, 2017 05 15.
Article em En | MEDLINE | ID: mdl-28432214
ABSTRACT
Here we present a parallel study of mRNA and microRNA expression during oral siphon (OS) regeneration in Ciona robusta, and the derived network of their interactions. In the process of identifying 248 mRNAs and 15 microRNAs as differentially expressed, we also identified 57 novel microRNAs, several of which are among the most highly differentially expressed. Analysis of functional categories identified enriched transcripts related to stress responses and apoptosis at the wound healing stage, signaling pathways including Wnt and TGFß during early regrowth, and negative regulation of extracellular proteases in late stage regeneration. Consistent with the expression results, we found that inhibition of TGFß signaling blocked OS regeneration. A correlation network was subsequently inferred for all predicted microRNA-mRNA target pairs expressed during regeneration. Network-based clustering associated transcripts into 22 non-overlapping groups, the functional analysis of which showed enrichment of stress response, signaling pathway and extracellular protease categories that could be related to specific microRNAs. Predicted targets of the miR-9 cluster suggest a role in regulating differentiation and the proliferative state of neural progenitors through regulation of the cytoskeleton and cell cycle.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Regeneração / Cicatrização / RNA Mensageiro / Ciona intestinalis / MicroRNAs / Redes Reguladoras de Genes / Boca Limite: Animals Idioma: En Revista: Development Assunto da revista: BIOLOGIA / EMBRIOLOGIA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Regeneração / Cicatrização / RNA Mensageiro / Ciona intestinalis / MicroRNAs / Redes Reguladoras de Genes / Boca Limite: Animals Idioma: En Revista: Development Assunto da revista: BIOLOGIA / EMBRIOLOGIA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos