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Mycoplasma non-coding RNA: identification of small RNAs and targets.
Siqueira, Franciele Maboni; de Morais, Guilherme Loss; Higashi, Susan; Beier, Laura Scherer; Breyer, Gabriela Merker; de Sá Godinho, Caio Padoan; Sagot, Marie-France; Schrank, Irene Silveira; Zaha, Arnaldo; de Vasconcelos, Ana Tereza Ribeiro.
Afiliação
  • Siqueira FM; Centro de Biotecnologia (CBiot), Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, Rio Grande do Sul, Brazil.
  • de Morais GL; Laboratório Nacional de Computação Científica (LNCC), Laboratório de Bioinformática (LABINFO), Petrópolis, Rio de Janeiro, Brazil.
  • Higashi S; Inria Grenoble Rhône-Alpes, 38330, Montbonnot Saint-Martin, France.
  • Beier LS; Université Lyon 1, Villeurbanne, France.
  • Breyer GM; CNRS, UMR5558, Laboratoire de Biométrie et Biologie Évolutive, F-69622, Villeurbanne, France.
  • de Sá Godinho CP; Centro de Biotecnologia (CBiot), Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, Rio Grande do Sul, Brazil.
  • Sagot MF; Centro de Biotecnologia (CBiot), Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, Rio Grande do Sul, Brazil.
  • Schrank IS; Laboratório Nacional de Computação Científica (LNCC), Laboratório de Bioinformática (LABINFO), Petrópolis, Rio de Janeiro, Brazil.
  • Zaha A; Inria Grenoble Rhône-Alpes, 38330, Montbonnot Saint-Martin, France.
  • de Vasconcelos AT; Université Lyon 1, Villeurbanne, France.
BMC Genomics ; 17(Suppl 8): 743, 2016 10 25.
Article em En | MEDLINE | ID: mdl-27801290
ABSTRACT

BACKGROUND:

Bacterial non-coding RNAs act by base-pairing as regulatory elements in crucial biological processes. We performed the identification of trans-encoded small RNAs (sRNA) from the genomes of Mycoplama hyopneumoniae, Mycoplasma flocculare and Mycoplasma hyorhinis, which are Mycoplasma species that have been identified in the porcine respiratory system.

RESULTS:

A total of 47, 15 and 11 putative sRNAs were predicted in M. hyopneumoniae, M. flocculare and M. hyorhinis, respectively. A comparative genomic analysis revealed the presence of species or lineage specific sRNA candidates. Furthermore, the expression profile of some M. hyopneumoniae sRNAs was determined by a reverse transcription amplification approach, in three different culture conditions. All tested sRNAs were transcribed in at least one condition. A detailed investigation revealed a differential expression profile for two M. hyopneumoniae sRNAs in response to oxidative and heat shock stress conditions, suggesting that their expression is influenced by environmental signals. Moreover, we analyzed sRNA-mRNA hybrids and accessed putative target genes for the novel sRNA candidates. The majority of the sRNAs showed interaction with multiple target genes, some of which could be linked to pathogenesis and cell homeostasis activity.

CONCLUSION:

This study contributes to our knowledge of Mycoplasma sRNAs and their response to environmental changes. Furthermore, the mRNA target prediction provides a perspective for the characterization and comprehension of the function of the sRNA regulatory mechanisms.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Regulação Bacteriana da Expressão Gênica / RNA não Traduzido / Interferência de RNA / Mycoplasma Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Regulação Bacteriana da Expressão Gênica / RNA não Traduzido / Interferência de RNA / Mycoplasma Idioma: En Ano de publicação: 2016 Tipo de documento: Article