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Differential transcription of expanded gene families in central carbon metabolism of Streptomyces coelicolor A3(2)
BACKGROUND: Streptomycete bacteria are prolific producers of specialized metabolites, many of which have clinically relevant bioactivity. A striking feature of their genomes is the expansion of gene families that encode the same enzymatic function. Genes that undergo expansion events, either by hori...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Microbiology Society
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7494193/ https://www.ncbi.nlm.nih.gov/pubmed/32974587 http://dx.doi.org/10.1099/acmi.0.000122 |
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author | Schniete, Jana K. Reumerman, Richard Kerr, Leena Tucker, Nicholas P. Hunter, Iain S. Herron, Paul R. Hoskisson, Paul A. |
author_facet | Schniete, Jana K. Reumerman, Richard Kerr, Leena Tucker, Nicholas P. Hunter, Iain S. Herron, Paul R. Hoskisson, Paul A. |
author_sort | Schniete, Jana K. |
collection | PubMed |
description | BACKGROUND: Streptomycete bacteria are prolific producers of specialized metabolites, many of which have clinically relevant bioactivity. A striking feature of their genomes is the expansion of gene families that encode the same enzymatic function. Genes that undergo expansion events, either by horizontal gene transfer or duplication, can have a range of fates: genes can be lost, or they can undergo neo-functionalization or sub-functionalization. To test whether expanded gene families in Streptomyces exhibit differential expression, an RNA-Seq approach was used to examine cultures of wild-type Streptomyces coelicolor grown with either glucose or tween as the sole carbon source. RESULTS: RNA-Seq analysis showed that two-thirds of genes within expanded gene families show transcriptional differences when strains were grown on tween compared to glucose. In addition, expression of specialized metabolite gene clusters (actinorhodin, isorenieratane, coelichelin and a cryptic NRPS) was also influenced by carbon source. CONCLUSIONS: Expression of genes encoding the same enzymatic function had transcriptional differences when grown on different carbon sources. This transcriptional divergence enables partitioning to function under different physiological conditions. These approaches can inform metabolic engineering of industrial Streptomyces strains and may help develop cultivation conditions to activate the so-called silent biosynthetic gene clusters. |
format | Online Article Text |
id | pubmed-7494193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Microbiology Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-74941932020-09-23 Differential transcription of expanded gene families in central carbon metabolism of Streptomyces coelicolor A3(2) Schniete, Jana K. Reumerman, Richard Kerr, Leena Tucker, Nicholas P. Hunter, Iain S. Herron, Paul R. Hoskisson, Paul A. Access Microbiol Research Article BACKGROUND: Streptomycete bacteria are prolific producers of specialized metabolites, many of which have clinically relevant bioactivity. A striking feature of their genomes is the expansion of gene families that encode the same enzymatic function. Genes that undergo expansion events, either by horizontal gene transfer or duplication, can have a range of fates: genes can be lost, or they can undergo neo-functionalization or sub-functionalization. To test whether expanded gene families in Streptomyces exhibit differential expression, an RNA-Seq approach was used to examine cultures of wild-type Streptomyces coelicolor grown with either glucose or tween as the sole carbon source. RESULTS: RNA-Seq analysis showed that two-thirds of genes within expanded gene families show transcriptional differences when strains were grown on tween compared to glucose. In addition, expression of specialized metabolite gene clusters (actinorhodin, isorenieratane, coelichelin and a cryptic NRPS) was also influenced by carbon source. CONCLUSIONS: Expression of genes encoding the same enzymatic function had transcriptional differences when grown on different carbon sources. This transcriptional divergence enables partitioning to function under different physiological conditions. These approaches can inform metabolic engineering of industrial Streptomyces strains and may help develop cultivation conditions to activate the so-called silent biosynthetic gene clusters. Microbiology Society 2020-03-30 /pmc/articles/PMC7494193/ /pubmed/32974587 http://dx.doi.org/10.1099/acmi.0.000122 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License. This article was made open access via a Publish and Read agreement between the Microbiology Society and the corresponding author’s institution. |
spellingShingle | Research Article Schniete, Jana K. Reumerman, Richard Kerr, Leena Tucker, Nicholas P. Hunter, Iain S. Herron, Paul R. Hoskisson, Paul A. Differential transcription of expanded gene families in central carbon metabolism of Streptomyces coelicolor A3(2) |
title | Differential transcription of expanded gene families in central carbon metabolism of Streptomyces coelicolor A3(2) |
title_full | Differential transcription of expanded gene families in central carbon metabolism of Streptomyces coelicolor A3(2) |
title_fullStr | Differential transcription of expanded gene families in central carbon metabolism of Streptomyces coelicolor A3(2) |
title_full_unstemmed | Differential transcription of expanded gene families in central carbon metabolism of Streptomyces coelicolor A3(2) |
title_short | Differential transcription of expanded gene families in central carbon metabolism of Streptomyces coelicolor A3(2) |
title_sort | differential transcription of expanded gene families in central carbon metabolism of streptomyces coelicolor a3(2) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7494193/ https://www.ncbi.nlm.nih.gov/pubmed/32974587 http://dx.doi.org/10.1099/acmi.0.000122 |
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