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纤细栓菌从头转录组测序揭示了腺苷生物合成相关基因。

De novo transcriptome sequencing of Paecilomyces tenuipes revealed genes involved in adenosine biosynthesis.

机构信息

Ministry of Education Engineering Research Center of Bioreactor and Pharmaceutical Development, School of Life Science, Jilin Agricultural University, Changchun, Jilin 130118, P.R. China.

出版信息

Mol Med Rep. 2020 Nov;22(5):3976-3984. doi: 10.3892/mmr.2020.11477. Epub 2020 Sep 2.

DOI:10.3892/mmr.2020.11477
PMID:32901833
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7533470/
Abstract

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.

摘要

蛹虫草(Paecilomyces tenuipes)是一种中国药用真菌,由于其腺苷含量低,其在科学研究中的应用受到限制。为了提高腺苷的产量,本研究通过转录组分析研究了蛹虫草腺苷生物合成的基因网络。培养 24 小时(PT24)、102 小时(PT102)和 196 小时(PT192)的蛹虫草菌丝体进行 RNA 测序。总共获得了 13353 个 unigenes。根据序列相似性,将 8099 个 unigenes注释为已知蛋白质。在这 8099 个 unigenes中,基于基因本体论术语将 5123 个 unigenes赋予了功能,基于真核同源物组数据库对 4158 个 unigenes进行了注释。此外,1272 个 unigenes映射到 281 个京都基因与基因组百科全书途径。此外,还对三个文库的差异基因表达进行了分析。在 PT24 与 PT102、PT24 与 PT192 和 PT102 与 PT192 组之间分别检测到 601、1658 和 628 个差异表达基因(DEGs)。通过反转录-定量 PCR 分析了 14 个与蛹虫草腺苷生物合成密切相关的 DEGs 的表达水平。结果表明,两个 DEGs 与蛹虫草腺苷积累密切相关。本研究不仅提供了对蛹虫草遗传信息的深入了解,而且还可以为蛹虫草的研究提供帮助。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818a/7533470/9c694e0aefbe/MMR-22-05-3976-g08.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818a/7533470/25544c3a363f/MMR-22-05-3976-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818a/7533470/11c3228d393e/MMR-22-05-3976-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818a/7533470/a8a26c780fd9/MMR-22-05-3976-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818a/7533470/e017746b5688/MMR-22-05-3976-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818a/7533470/6266f5e2822d/MMR-22-05-3976-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818a/7533470/107dbadb6e4f/MMR-22-05-3976-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818a/7533470/1b055ffd5408/MMR-22-05-3976-g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818a/7533470/2edf0176b5d2/MMR-22-05-3976-g07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818a/7533470/9c694e0aefbe/MMR-22-05-3976-g08.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818a/7533470/25544c3a363f/MMR-22-05-3976-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818a/7533470/11c3228d393e/MMR-22-05-3976-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818a/7533470/a8a26c780fd9/MMR-22-05-3976-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818a/7533470/e017746b5688/MMR-22-05-3976-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818a/7533470/6266f5e2822d/MMR-22-05-3976-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818a/7533470/107dbadb6e4f/MMR-22-05-3976-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818a/7533470/1b055ffd5408/MMR-22-05-3976-g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818a/7533470/2edf0176b5d2/MMR-22-05-3976-g07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/818a/7533470/9c694e0aefbe/MMR-22-05-3976-g08.jpg

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2
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Genes (Basel). 2019 May 8;10(5):351. doi: 10.3390/genes10050351.
3
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4
New approach for understanding genome variations in KEGG.KEGG 中基因组变异的新方法。
Nucleic Acids Res. 2019 Jan 8;47(D1):D590-D595. doi: 10.1093/nar/gky962.
5
Improvement of industrially important microbial strains by genome shuffling: Current status and future prospects.通过基因组重排提高工业上重要的微生物菌株的性能:现状与展望。
Bioresour Technol. 2018 Jun;257:281-289. doi: 10.1016/j.biortech.2018.02.118. Epub 2018 Feb 27.
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