Interplay between non-coding RNA transcription, stringent phenotype and antibiotic production in Streptomyces.

Re-defined transcriptome Streptomyces antibiotic production ncRNA stringent response

Journal

Journal of biotechnology
ISSN: 1873-4863
Titre abrégé: J Biotechnol
Pays: Netherlands
ID NLM: 8411927

Informations de publication

Date de publication:
16 Feb 2022
Historique:
received: 15 01 2021
accepted: 12 02 2022
entrez: 19 2 2022
pubmed: 20 2 2022
medline: 20 2 2022
Statut: aheadofprint

Résumé

While in recent years the key role of non-coding RNAs (ncRNAs) in regulation of gene expression has become increasingly evident, their interaction with the global regulatory circuits is still obscure. Here we analyzed the structure and organization of the transcriptome of Streptomyces ambofaciens, the producer of spiramycin. We identified ncRNAs including 45 small-RNAs (sRNAs) and 119 antisense-RNAs (asRNAs I) that appear transcribed from dedicated promoters. Some sRNAs and asRNAs are unprecedented in Streptomyces, and were predicted to target mRNAs encoding proteins involved in transcription, translation, ribosomal structure and biogenesis, and regulation of morphological and biochemical differentiation. We then compared ncRNA expression in three strains: i.) the wild type strain; ii.) an isogenic pirA-defective mutant with central carbon metabolism imbalance, "relaxed" phenotype, and repression of antibiotic production; iii.) a pirA-derivative strain harboring a "stringent" RNA polymerase that suppresses pirA-associated phenotypes. Data indicated that expression of most ncRNAs was correlated to the stringent/relaxed phenotype suggesting novel effector mechanisms of the stringent response.

Identifiants

pubmed: 35182607
pii: S0168-1656(22)00029-3
doi: 10.1016/j.jbiotec.2022.02.006
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2022. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Eva Pinatel (E)

Institute of Biomedical Technologies, National Research Council, Segrate, Milan, Italy.

Matteo Calcagnile (M)

Department of Biological and Environmental Sciences and Technologies, University of Salento, Via Monteroni, 73100 Lecce, Italy.

Adelfia Talà (A)

Department of Biological and Environmental Sciences and Technologies, University of Salento, Via Monteroni, 73100 Lecce, Italy.

Fabrizio Damiano (F)

Department of Biological and Environmental Sciences and Technologies, University of Salento, Via Monteroni, 73100 Lecce, Italy.

Luisa Siculella (L)

Department of Biological and Environmental Sciences and Technologies, University of Salento, Via Monteroni, 73100 Lecce, Italy.

Clelia Peano (C)

Genomic Unit, IRCCS Humanitas Clinical and Research Center, Rozzano, Milan, Italy; Institute of Genetic and Biomedical Research, UoS of Milan, National Research Council, Rozzano, Milan, Italy.

Giuseppe Egidio De Benedetto (GE)

Department of Cultural Heritage, University of Salento, Via Monteroni, 73100 Lecce, Italy.

Antonio Pennetta (A)

Department of Cultural Heritage, University of Salento, Via Monteroni, 73100 Lecce, Italy.

Gianluca De Bellis (G)

Institute of Biomedical Technologies, National Research Council, Segrate, Milan, Italy.

Pietro Alifano (P)

Department of Biological and Environmental Sciences and Technologies, University of Salento, Via Monteroni, 73100 Lecce, Italy. Electronic address: pietro.alifano@unisalento.it.

Classifications MeSH