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A fungal transcription factor essential for starch degradation affects integration of carbon and nitrogen metabolism
In Neurospora crassa, the transcription factor COL-26 functions as a regulator of glucose signaling and metabolism. Its loss leads to resistance to carbon catabolite repression. Here, we report that COL-26 is necessary for the expression of amylolytic genes in N. crassa and is required for the utili...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5435353/ https://www.ncbi.nlm.nih.gov/pubmed/28467421 http://dx.doi.org/10.1371/journal.pgen.1006737 |
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author | Xiong, Yi Wu, Vincent W. Lubbe, Andrea Qin, Lina Deng, Siwen Kennedy, Megan Bauer, Diane Singan, Vasanth R. Barry, Kerrie Northen, Trent R. Grigoriev, Igor V. Glass, N. Louise |
author_facet | Xiong, Yi Wu, Vincent W. Lubbe, Andrea Qin, Lina Deng, Siwen Kennedy, Megan Bauer, Diane Singan, Vasanth R. Barry, Kerrie Northen, Trent R. Grigoriev, Igor V. Glass, N. Louise |
author_sort | Xiong, Yi |
collection | PubMed |
description | In Neurospora crassa, the transcription factor COL-26 functions as a regulator of glucose signaling and metabolism. Its loss leads to resistance to carbon catabolite repression. Here, we report that COL-26 is necessary for the expression of amylolytic genes in N. crassa and is required for the utilization of maltose and starch. Additionally, the Δcol-26 mutant shows growth defects on preferred carbon sources, such as glucose, an effect that was alleviated if glutamine replaced ammonium as the primary nitrogen source. This rescue did not occur when maltose was used as a sole carbon source. Transcriptome and metabolic analyses of the Δcol-26 mutant relative to its wild type parental strain revealed that amino acid and nitrogen metabolism, the TCA cycle and GABA shunt were adversely affected. Phylogenetic analysis showed a single col-26 homolog in Sordariales, Ophilostomatales, and the Magnaporthales, but an expanded number of col-26 homologs in other filamentous fungal species. Deletion of the closest homolog of col-26 in Trichoderma reesei, bglR, resulted in a mutant with similar preferred carbon source growth deficiency, and which was alleviated if glutamine was the sole nitrogen source, suggesting conservation of COL-26 and BglR function. Our finding provides novel insight into the role of COL-26 for utilization of starch and in integrating carbon and nitrogen metabolism for balanced metabolic activities for optimal carbon and nitrogen distribution. |
format | Online Article Text |
id | pubmed-5435353 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-54353532017-05-27 A fungal transcription factor essential for starch degradation affects integration of carbon and nitrogen metabolism Xiong, Yi Wu, Vincent W. Lubbe, Andrea Qin, Lina Deng, Siwen Kennedy, Megan Bauer, Diane Singan, Vasanth R. Barry, Kerrie Northen, Trent R. Grigoriev, Igor V. Glass, N. Louise PLoS Genet Research Article In Neurospora crassa, the transcription factor COL-26 functions as a regulator of glucose signaling and metabolism. Its loss leads to resistance to carbon catabolite repression. Here, we report that COL-26 is necessary for the expression of amylolytic genes in N. crassa and is required for the utilization of maltose and starch. Additionally, the Δcol-26 mutant shows growth defects on preferred carbon sources, such as glucose, an effect that was alleviated if glutamine replaced ammonium as the primary nitrogen source. This rescue did not occur when maltose was used as a sole carbon source. Transcriptome and metabolic analyses of the Δcol-26 mutant relative to its wild type parental strain revealed that amino acid and nitrogen metabolism, the TCA cycle and GABA shunt were adversely affected. Phylogenetic analysis showed a single col-26 homolog in Sordariales, Ophilostomatales, and the Magnaporthales, but an expanded number of col-26 homologs in other filamentous fungal species. Deletion of the closest homolog of col-26 in Trichoderma reesei, bglR, resulted in a mutant with similar preferred carbon source growth deficiency, and which was alleviated if glutamine was the sole nitrogen source, suggesting conservation of COL-26 and BglR function. Our finding provides novel insight into the role of COL-26 for utilization of starch and in integrating carbon and nitrogen metabolism for balanced metabolic activities for optimal carbon and nitrogen distribution. Public Library of Science 2017-05-03 /pmc/articles/PMC5435353/ /pubmed/28467421 http://dx.doi.org/10.1371/journal.pgen.1006737 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Xiong, Yi Wu, Vincent W. Lubbe, Andrea Qin, Lina Deng, Siwen Kennedy, Megan Bauer, Diane Singan, Vasanth R. Barry, Kerrie Northen, Trent R. Grigoriev, Igor V. Glass, N. Louise A fungal transcription factor essential for starch degradation affects integration of carbon and nitrogen metabolism |
title | A fungal transcription factor essential for starch degradation affects integration of carbon and nitrogen metabolism |
title_full | A fungal transcription factor essential for starch degradation affects integration of carbon and nitrogen metabolism |
title_fullStr | A fungal transcription factor essential for starch degradation affects integration of carbon and nitrogen metabolism |
title_full_unstemmed | A fungal transcription factor essential for starch degradation affects integration of carbon and nitrogen metabolism |
title_short | A fungal transcription factor essential for starch degradation affects integration of carbon and nitrogen metabolism |
title_sort | fungal transcription factor essential for starch degradation affects integration of carbon and nitrogen metabolism |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5435353/ https://www.ncbi.nlm.nih.gov/pubmed/28467421 http://dx.doi.org/10.1371/journal.pgen.1006737 |
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