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Extracellular DNA secreted in yeast cultures is metabolism-specific and inhibits cell proliferation
Extracellular DNA (exDNA) can be actively released by living cells and different putative functions have been attributed to it. Further, homologous exDNA has been reported to exert species-specific inhibitory effects on several organisms. Here, we demonstrate by different experimental evidence, incl...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shared Science Publishers OG
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10695634/ http://dx.doi.org/10.15698/mic2023.12.810 |
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author | de Alteriis, Elisabetta Incerti, Guido Cartenì, Fabrizio Chiusano, Maria Luisa Colantuono, Chiara Palomba, Emanuela Termolino, Pasquale Monticolo, Francesco Esposito, Alfonso Bonanomi, Giuliano Capparelli, Rosanna Iannaccone, Marco Foscari, Alessandro Landi, Carmine Parascandola, Palma Sanchez, Massimo Tirelli, Valentina de Falco, Bruna Lanzotti, Virginia Mazzoleni, Stefano |
author_facet | de Alteriis, Elisabetta Incerti, Guido Cartenì, Fabrizio Chiusano, Maria Luisa Colantuono, Chiara Palomba, Emanuela Termolino, Pasquale Monticolo, Francesco Esposito, Alfonso Bonanomi, Giuliano Capparelli, Rosanna Iannaccone, Marco Foscari, Alessandro Landi, Carmine Parascandola, Palma Sanchez, Massimo Tirelli, Valentina de Falco, Bruna Lanzotti, Virginia Mazzoleni, Stefano |
author_sort | de Alteriis, Elisabetta |
collection | PubMed |
description | Extracellular DNA (exDNA) can be actively released by living cells and different putative functions have been attributed to it. Further, homologous exDNA has been reported to exert species-specific inhibitory effects on several organisms. Here, we demonstrate by different experimental evidence, including (1)H-NMR metabolomic fingerprint, that the growth rate decline in Saccharomyces cerevisiae fed-batch cultures is determined by the accumulation of exDNA in the medium. Sequencing of such secreted exDNA represents a portion of the entire genome, showing a great similarity with extrachromosomal circular DNA (eccDNA) already reported inside yeast cells. The recovered DNA molecules were mostly single strands and specifically associated to the yeast metabolism displayed during cell growth. Flow cytometric analysis showed that the observed growth inhibition by exDNA corresponded to an arrest in the S phase of the cell cycle. These unprecedented findings open a new scenario on the functional role of exDNA produced by living cells. |
format | Online Article Text |
id | pubmed-10695634 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Shared Science Publishers OG |
record_format | MEDLINE/PubMed |
spelling | pubmed-106956342023-12-05 Extracellular DNA secreted in yeast cultures is metabolism-specific and inhibits cell proliferation de Alteriis, Elisabetta Incerti, Guido Cartenì, Fabrizio Chiusano, Maria Luisa Colantuono, Chiara Palomba, Emanuela Termolino, Pasquale Monticolo, Francesco Esposito, Alfonso Bonanomi, Giuliano Capparelli, Rosanna Iannaccone, Marco Foscari, Alessandro Landi, Carmine Parascandola, Palma Sanchez, Massimo Tirelli, Valentina de Falco, Bruna Lanzotti, Virginia Mazzoleni, Stefano Microb Cell Research Article Extracellular DNA (exDNA) can be actively released by living cells and different putative functions have been attributed to it. Further, homologous exDNA has been reported to exert species-specific inhibitory effects on several organisms. Here, we demonstrate by different experimental evidence, including (1)H-NMR metabolomic fingerprint, that the growth rate decline in Saccharomyces cerevisiae fed-batch cultures is determined by the accumulation of exDNA in the medium. Sequencing of such secreted exDNA represents a portion of the entire genome, showing a great similarity with extrachromosomal circular DNA (eccDNA) already reported inside yeast cells. The recovered DNA molecules were mostly single strands and specifically associated to the yeast metabolism displayed during cell growth. Flow cytometric analysis showed that the observed growth inhibition by exDNA corresponded to an arrest in the S phase of the cell cycle. These unprecedented findings open a new scenario on the functional role of exDNA produced by living cells. Shared Science Publishers OG 2023-11-23 /pmc/articles/PMC10695634/ http://dx.doi.org/10.15698/mic2023.12.810 Text en Copyright: © 2023 de Alteriis et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article released under the terms of the Creative Commons Attribution (CC BY) license, which allows the unrestricted use, distribution, and reproduction in any medium, provided the original author and source are acknowledged. |
spellingShingle | Research Article de Alteriis, Elisabetta Incerti, Guido Cartenì, Fabrizio Chiusano, Maria Luisa Colantuono, Chiara Palomba, Emanuela Termolino, Pasquale Monticolo, Francesco Esposito, Alfonso Bonanomi, Giuliano Capparelli, Rosanna Iannaccone, Marco Foscari, Alessandro Landi, Carmine Parascandola, Palma Sanchez, Massimo Tirelli, Valentina de Falco, Bruna Lanzotti, Virginia Mazzoleni, Stefano Extracellular DNA secreted in yeast cultures is metabolism-specific and inhibits cell proliferation |
title | Extracellular DNA secreted in yeast cultures is metabolism-specific and inhibits cell proliferation |
title_full | Extracellular DNA secreted in yeast cultures is metabolism-specific and inhibits cell proliferation |
title_fullStr | Extracellular DNA secreted in yeast cultures is metabolism-specific and inhibits cell proliferation |
title_full_unstemmed | Extracellular DNA secreted in yeast cultures is metabolism-specific and inhibits cell proliferation |
title_short | Extracellular DNA secreted in yeast cultures is metabolism-specific and inhibits cell proliferation |
title_sort | extracellular dna secreted in yeast cultures is metabolism-specific and inhibits cell proliferation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10695634/ http://dx.doi.org/10.15698/mic2023.12.810 |
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