Transcriptome Comparison of Secondary Metabolite Biosynthesis Genes Expressed in Cultured and Lichenized Conditions of Cladonia rangiferina

Lichen secondary metabolites are natural products of high medicinal and industrial value, which are produced by the fungal symbiont (mycobiont) of lichens in response to environmental changes. It has been shown that the cultured mycobiont is capable of secondary metabolite production, specifically p...

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Published in:Diversity
Main Authors: Natalia Sveshnikova, Michele D. Piercey-Normore
Format: Text
Language:English
Published: Multidisciplinary Digital Publishing Institute 2021
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Online Access:https://doi.org/10.3390/d13110529
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author Natalia Sveshnikova
Michele D. Piercey-Normore
author_facet Natalia Sveshnikova
Michele D. Piercey-Normore
author_sort Natalia Sveshnikova
collection MDPI Open Access Publishing
container_issue 11
container_start_page 529
container_title Diversity
container_volume 13
description Lichen secondary metabolites are natural products of high medicinal and industrial value, which are produced by the fungal symbiont (mycobiont) of lichens in response to environmental changes. It has been shown that the cultured mycobiont is capable of secondary metabolite production, specifically polyketides, and polyketide production is affected by the presence or absence of the algal or cyanobacterial symbiont (photobiont). Identification of polyketide synthases encoding genes is, in turn, key for understanding the regulation of secondary metabolite synthesis. Using a previously established method of resynthesis for Cladonia rangiferina as well as the sequenced and assembled genome of that species, we compared transcriptomes of C. rangiferina cultured alone and resynthesized with the photobiont (Asterochloris glomerata) to reveal transcriptionally active genes in secondary metabolic gene clusters, as well some of the neighbouring genes, induced by the presence of the photobiont and events of lichenization. The results identify potential candidates for PKS genes in C. rangiferina, identify potential neighbouring genes in the PKS cluster, and offer insights into further research. The study provides preliminary insights into the activity of several identified biosynthetic gene clusters (BGC) as well as interactions of genes within those clusters.
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https://dx.doi.org/10.3390/d13110529
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op_source Diversity; Volume 13; Issue 11; Pages: 529
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spelling ftmdpi:oai:mdpi.com:/1424-2818/13/11/529/ 2025-01-16T21:31:29+00:00 Transcriptome Comparison of Secondary Metabolite Biosynthesis Genes Expressed in Cultured and Lichenized Conditions of Cladonia rangiferina Natalia Sveshnikova Michele D. Piercey-Normore agris 2021-10-24 application/pdf https://doi.org/10.3390/d13110529 EN eng Multidisciplinary Digital Publishing Institute Plant Diversity https://dx.doi.org/10.3390/d13110529 https://creativecommons.org/licenses/by/4.0/ Diversity; Volume 13; Issue 11; Pages: 529 Cladonia rangiferina lichen-forming fungi transcriptomics lichen secondary metabolites polyketide synthases PKS gene expression lichenization resynthesis Text 2021 ftmdpi https://doi.org/10.3390/d13110529 2023-08-01T03:03:05Z Lichen secondary metabolites are natural products of high medicinal and industrial value, which are produced by the fungal symbiont (mycobiont) of lichens in response to environmental changes. It has been shown that the cultured mycobiont is capable of secondary metabolite production, specifically polyketides, and polyketide production is affected by the presence or absence of the algal or cyanobacterial symbiont (photobiont). Identification of polyketide synthases encoding genes is, in turn, key for understanding the regulation of secondary metabolite synthesis. Using a previously established method of resynthesis for Cladonia rangiferina as well as the sequenced and assembled genome of that species, we compared transcriptomes of C. rangiferina cultured alone and resynthesized with the photobiont (Asterochloris glomerata) to reveal transcriptionally active genes in secondary metabolic gene clusters, as well some of the neighbouring genes, induced by the presence of the photobiont and events of lichenization. The results identify potential candidates for PKS genes in C. rangiferina, identify potential neighbouring genes in the PKS cluster, and offer insights into further research. The study provides preliminary insights into the activity of several identified biosynthetic gene clusters (BGC) as well as interactions of genes within those clusters. Text Cladonia rangiferina MDPI Open Access Publishing Diversity 13 11 529
spellingShingle Cladonia rangiferina
lichen-forming fungi
transcriptomics
lichen secondary metabolites
polyketide synthases
PKS
gene expression
lichenization
resynthesis
Natalia Sveshnikova
Michele D. Piercey-Normore
Transcriptome Comparison of Secondary Metabolite Biosynthesis Genes Expressed in Cultured and Lichenized Conditions of Cladonia rangiferina
title Transcriptome Comparison of Secondary Metabolite Biosynthesis Genes Expressed in Cultured and Lichenized Conditions of Cladonia rangiferina
title_full Transcriptome Comparison of Secondary Metabolite Biosynthesis Genes Expressed in Cultured and Lichenized Conditions of Cladonia rangiferina
title_fullStr Transcriptome Comparison of Secondary Metabolite Biosynthesis Genes Expressed in Cultured and Lichenized Conditions of Cladonia rangiferina
title_full_unstemmed Transcriptome Comparison of Secondary Metabolite Biosynthesis Genes Expressed in Cultured and Lichenized Conditions of Cladonia rangiferina
title_short Transcriptome Comparison of Secondary Metabolite Biosynthesis Genes Expressed in Cultured and Lichenized Conditions of Cladonia rangiferina
title_sort transcriptome comparison of secondary metabolite biosynthesis genes expressed in cultured and lichenized conditions of cladonia rangiferina
topic Cladonia rangiferina
lichen-forming fungi
transcriptomics
lichen secondary metabolites
polyketide synthases
PKS
gene expression
lichenization
resynthesis
topic_facet Cladonia rangiferina
lichen-forming fungi
transcriptomics
lichen secondary metabolites
polyketide synthases
PKS
gene expression
lichenization
resynthesis
url https://doi.org/10.3390/d13110529