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De novo transcriptome sequencing of Paecilomyces tenuipes revealed genes involved in adenosine biosynthesis
The use of Paecilomyces tenuipes (P. tenuipes), a Chinese medicinal fungus in scientific research, is limited due to its low adenosine content. To improve adenosine production, the present study investigated the gene network of adenosine biosynthesis in P. tenuipes via transcriptome analysis. Myceli...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533470/ https://www.ncbi.nlm.nih.gov/pubmed/32901833 http://dx.doi.org/10.3892/mmr.2020.11477 |
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author | Han, Long Li, Yaying Meng, Xinyu Chu, Guodong Guo, Yongxin Noman, Muhammad Dong, Yuanyuan Li, Haiyan Yang, Jing Du, Linna |
author_facet | Han, Long Li, Yaying Meng, Xinyu Chu, Guodong Guo, Yongxin Noman, Muhammad Dong, Yuanyuan Li, Haiyan Yang, Jing Du, Linna |
author_sort | Han, Long |
collection | PubMed |
description | The use of Paecilomyces tenuipes (P. tenuipes), a Chinese medicinal fungus in scientific research, is limited due to its low adenosine content. To improve adenosine production, the present study investigated the gene network of adenosine biosynthesis in P. tenuipes via transcriptome analysis. Mycelia of P. tenuipes cultured for 24 h (PT24), 102 h (PT102) and 196 h (PT192) were subjected to RNA sequencing. In total, 13,353 unigenes were obtained. Based on sequence similarity, 8,099 unigenes were annotated with known proteins. Of these 8,099 unigenes, 5,123 had functions assigned based on Gene Ontology terms while 4,158 were annotated based on the Eukaryotic Orthologous Groups database. Moreover, 1,272 unigenes were mapped to 281 Kyoto Encyclopedia of Genes and Genomes pathways. In addition, the differential gene expression of the three libraries was also performed. A total of 601, 1,658 and 628 differentially expressed genes (DEGs) were detected in PT24 vs. PT102, PT24 vs. PT192 and PT102 vs. PT192 groups, respectively. Reverse transcription-quantitative PCR was performed to analyze the expression levels of 14 DEGs putatively associated with adenosine biosynthesis in P. tenuipes. The results showed that two DEGs were closely associated with adenosine accumulation of P. tenuipes. The present study not only provides an improved understanding of the genetic information of P. tenuipes but also the findings can be used to aid research into P. tenuipes. |
format | Online Article Text |
id | pubmed-7533470 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-75334702020-10-07 De novo transcriptome sequencing of Paecilomyces tenuipes revealed genes involved in adenosine biosynthesis Han, Long Li, Yaying Meng, Xinyu Chu, Guodong Guo, Yongxin Noman, Muhammad Dong, Yuanyuan Li, Haiyan Yang, Jing Du, Linna Mol Med Rep Articles The use of Paecilomyces tenuipes (P. tenuipes), a Chinese medicinal fungus in scientific research, is limited due to its low adenosine content. To improve adenosine production, the present study investigated the gene network of adenosine biosynthesis in P. tenuipes via transcriptome analysis. Mycelia of P. tenuipes cultured for 24 h (PT24), 102 h (PT102) and 196 h (PT192) were subjected to RNA sequencing. In total, 13,353 unigenes were obtained. Based on sequence similarity, 8,099 unigenes were annotated with known proteins. Of these 8,099 unigenes, 5,123 had functions assigned based on Gene Ontology terms while 4,158 were annotated based on the Eukaryotic Orthologous Groups database. Moreover, 1,272 unigenes were mapped to 281 Kyoto Encyclopedia of Genes and Genomes pathways. In addition, the differential gene expression of the three libraries was also performed. A total of 601, 1,658 and 628 differentially expressed genes (DEGs) were detected in PT24 vs. PT102, PT24 vs. PT192 and PT102 vs. PT192 groups, respectively. Reverse transcription-quantitative PCR was performed to analyze the expression levels of 14 DEGs putatively associated with adenosine biosynthesis in P. tenuipes. The results showed that two DEGs were closely associated with adenosine accumulation of P. tenuipes. The present study not only provides an improved understanding of the genetic information of P. tenuipes but also the findings can be used to aid research into P. tenuipes. D.A. Spandidos 2020-11 2020-09-02 /pmc/articles/PMC7533470/ /pubmed/32901833 http://dx.doi.org/10.3892/mmr.2020.11477 Text en Copyright: © Han et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Han, Long Li, Yaying Meng, Xinyu Chu, Guodong Guo, Yongxin Noman, Muhammad Dong, Yuanyuan Li, Haiyan Yang, Jing Du, Linna De novo transcriptome sequencing of Paecilomyces tenuipes revealed genes involved in adenosine biosynthesis |
title | De novo transcriptome sequencing of Paecilomyces tenuipes revealed genes involved in adenosine biosynthesis |
title_full | De novo transcriptome sequencing of Paecilomyces tenuipes revealed genes involved in adenosine biosynthesis |
title_fullStr | De novo transcriptome sequencing of Paecilomyces tenuipes revealed genes involved in adenosine biosynthesis |
title_full_unstemmed | De novo transcriptome sequencing of Paecilomyces tenuipes revealed genes involved in adenosine biosynthesis |
title_short | De novo transcriptome sequencing of Paecilomyces tenuipes revealed genes involved in adenosine biosynthesis |
title_sort | de novo transcriptome sequencing of paecilomyces tenuipes revealed genes involved in adenosine biosynthesis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533470/ https://www.ncbi.nlm.nih.gov/pubmed/32901833 http://dx.doi.org/10.3892/mmr.2020.11477 |
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