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Transcriptome-wide analysis reveals the progress of Cordyceps militaris subculture degeneration
BACKGROUND: The entomopathogenic mushroom Cordyceps militaris is an important medicinal and food resource owing to its various medicinal components and pharmacological effects. However, the high frequency of strain degeneration during subculture seriously restricts the large-scale production of C. m...
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/PMC5657973/ https://www.ncbi.nlm.nih.gov/pubmed/29073171 http://dx.doi.org/10.1371/journal.pone.0186279 |
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author | Yin, Juan Xin, Xiangdong Weng, Yujie Gui, Zhongzheng |
author_facet | Yin, Juan Xin, Xiangdong Weng, Yujie Gui, Zhongzheng |
author_sort | Yin, Juan |
collection | PubMed |
description | BACKGROUND: The entomopathogenic mushroom Cordyceps militaris is an important medicinal and food resource owing to its various medicinal components and pharmacological effects. However, the high frequency of strain degeneration during subculture seriously restricts the large-scale production of C. militaris, and the mechanism underlying strain degeneration remains unclear. In this study, we artificially cultured C. militaris for six generations and compared changes during fruiting body growth. The transcriptome of six generations of C. militaris strains were sequenced with the Illumine Hiseq4000. RESULTS: The subcultured C. militaris strains degenerated beginning at the third generation, with incomplete fruiting body growth beginning at the fourth generation. Over 9,015 unigenes and 731 new genes were identified. In addition, 35,323 alternative splicing (AS) events were detected in all samples, and more AS events occurred in the second, fourth and sixth generations. Compared with the first generation, the third generation (degenerated strain) included 2,498 differentially expressed genes (DEGs) including 1,729 up-regulated and 769 down-regulated genes. This number was higher than the number of DEGs in the second (1,892 DEGs), fourth (2,006 DEGs), fifth (2,273 DEGs) and sixth (2,188 DEGs) generations. Validation of RNA-seq by qRT-PCR showed that the expression patterns of 51 DEGs were in accordance with the transcriptome data. CONCLUSION: Our results suggest that the mechanism of C. militaris strain degeneration is associated with gene involved in toxin biosynthesis, energy metabolism, and DNA methylation and chromosome remodeling. |
format | Online Article Text |
id | pubmed-5657973 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56579732017-11-09 Transcriptome-wide analysis reveals the progress of Cordyceps militaris subculture degeneration Yin, Juan Xin, Xiangdong Weng, Yujie Gui, Zhongzheng PLoS One Research Article BACKGROUND: The entomopathogenic mushroom Cordyceps militaris is an important medicinal and food resource owing to its various medicinal components and pharmacological effects. However, the high frequency of strain degeneration during subculture seriously restricts the large-scale production of C. militaris, and the mechanism underlying strain degeneration remains unclear. In this study, we artificially cultured C. militaris for six generations and compared changes during fruiting body growth. The transcriptome of six generations of C. militaris strains were sequenced with the Illumine Hiseq4000. RESULTS: The subcultured C. militaris strains degenerated beginning at the third generation, with incomplete fruiting body growth beginning at the fourth generation. Over 9,015 unigenes and 731 new genes were identified. In addition, 35,323 alternative splicing (AS) events were detected in all samples, and more AS events occurred in the second, fourth and sixth generations. Compared with the first generation, the third generation (degenerated strain) included 2,498 differentially expressed genes (DEGs) including 1,729 up-regulated and 769 down-regulated genes. This number was higher than the number of DEGs in the second (1,892 DEGs), fourth (2,006 DEGs), fifth (2,273 DEGs) and sixth (2,188 DEGs) generations. Validation of RNA-seq by qRT-PCR showed that the expression patterns of 51 DEGs were in accordance with the transcriptome data. CONCLUSION: Our results suggest that the mechanism of C. militaris strain degeneration is associated with gene involved in toxin biosynthesis, energy metabolism, and DNA methylation and chromosome remodeling. Public Library of Science 2017-10-26 /pmc/articles/PMC5657973/ /pubmed/29073171 http://dx.doi.org/10.1371/journal.pone.0186279 Text en © 2017 Yin et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Yin, Juan Xin, Xiangdong Weng, Yujie Gui, Zhongzheng Transcriptome-wide analysis reveals the progress of Cordyceps militaris subculture degeneration |
title | Transcriptome-wide analysis reveals the progress of Cordyceps militaris subculture degeneration |
title_full | Transcriptome-wide analysis reveals the progress of Cordyceps militaris subculture degeneration |
title_fullStr | Transcriptome-wide analysis reveals the progress of Cordyceps militaris subculture degeneration |
title_full_unstemmed | Transcriptome-wide analysis reveals the progress of Cordyceps militaris subculture degeneration |
title_short | Transcriptome-wide analysis reveals the progress of Cordyceps militaris subculture degeneration |
title_sort | transcriptome-wide analysis reveals the progress of cordyceps militaris subculture degeneration |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5657973/ https://www.ncbi.nlm.nih.gov/pubmed/29073171 http://dx.doi.org/10.1371/journal.pone.0186279 |
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