Evidence map›Paper›PMID 27551021›Full record

ArticleJournal of bacteriology2016

The Coordinated Positive Regulation of Topoisomerase Genes Maintains Topological Homeostasis in Streptomyces coelicolor.

Marcin Jan Szafran, Martyna Gongerowska, Paweł Gutkowski, Jolanta Zakrzewska-Czerwińska, Dagmara Jakimowicz

Open access · hybridAbstract read
In one paragraph

Article in Journal of bacteriology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. The regulation of DNA supercoiling across evolution.Protein science : a publication of the Protein Society · 2021
    Review
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  11. Transcriptional Response ofFrontiers in microbiology · 2019
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Marcin Jan SzafranUniversity of Wroclaw, Faculty of Biotechnology, Laboratory of Molecular Microbiology, Wroclaw, Poland marcin.szafran@uwr.edu.pl.
Martyna GongerowskaUniversity of Wroclaw, Faculty of Biotechnology, Laboratory of Molecular Microbiology, Wroclaw, Poland.
Paweł GutkowskiWroclaw University of Technology, Faculty of Chemistry, Wroclaw, Poland.
Jolanta Zakrzewska-CzerwińskaUniversity of Wroclaw, Faculty of Biotechnology, Laboratory of Molecular Microbiology, Wroclaw, Poland Institute of Immunology and Experimental Therapy, Laboratory of Microbiology, Wroclaw, Poland.
Dagmara JakimowiczUniversity of Wroclaw, Faculty of Biotechnology, Laboratory of Molecular Microbiology, Wroclaw, Poland Institute of Immunology and Experimental Therapy, Laboratory of Microbiology, Wroclaw, Poland.
University of Wrocław · PLLudwik Hirszfeld Institute of Immunology and Experimental Therapy · PLWrocław University of Science and Technology · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Maintaining an optimal level of chromosomal supercoiling is critical for the progression of DNA replication and transcription. Moreover, changes in global supercoiling affect the expression of a large number of genes and play a fundamental role in adapting to stress. Topoisomerase I (TopA) and gyrase are key players in the regulation of bacterial chromosomal topology through their respective abilities to relax and compact DNA. Soil bacteria such as Streptomyces species, which grow as branched, multigenomic hyphae, are subject to environmental stresses that are associated with changes in chromosomal topology. The topological fluctuations modulate the transcriptional activity of a large number of genes and in Streptomyces are related to the production of antibiotics. To better understand the regulation of topological homeostasis in Streptomyces coelicolor, we investigated the interplay between the activities of the topoisomerase-encoding genes topA and gyrBA We show that the expression of both genes is supercoiling sensitive. Remarkably, increased chromosomal supercoiling induces the topA promoter but only slightly influences gyrBA transcription, while DNA relaxation affects the topA promoter only marginally but strongly activates the gyrBA operon. Moreover, we showed that exposure to elevated temperatures induces rapid relaxation, which results in changes in the levels of both topoisomerases. We therefore propose a unique mechanism of S. coelicolor chromosomal topology maintenance based on the supercoiling-dependent stimulation, rather than repression, of the transcription of both topoisomerase genes. These findings provide important insight into the maintenance of topological homeostasis in an industrially important antibiotic producer. IMPORTANCE: We describe the unique regulation of genes encoding two topoisomerases, topoisomerase I (TopA) and gyrase, in a model Streptomyces species. Our studies demonstrate the coordination of topoisomerase gene regulation, which is crucial for maintenance of topological homeostasis. Streptomyces species are producers of a plethora of biologically active secondary metabolites, including antibiotics, antitumor agents, and immunosuppressants. The significant regulatory factor controlling the secondary metabolism is the global chromosomal topology. Thus, the investigation of chromosomal topology homeostasis in Streptomyces strains is crucial for their use in industrial applications as producers of secondary metabolites.

Indexed as

Gene Expression Regulation, EnzymologicBacterial ProteinsDNA, BacterialDNA GyraseDNA, SuperhelicalDNA Topoisomerases, Type IGene Expression Regulation, BacterialHomeostasisOperonPromoter Regions, GeneticStreptomyces coelicolorTranscription, GeneticBacterial ProteinsDNA, BacterialDNA GyraseDNA, SuperhelicalDNA Topoisomerases, Type I

Identifiers

PMID27551021
PMCPMC5055605
OpenAlexW2510790595

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.