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De novo transcriptome assembly and comprehensive assessment provide insight into fruiting body formation of Sparassis latifolia

The genes associated with fruiting body formation of Sparasis latifolia are valuable for improving mushroom breeding. To investigate this process, 4.8 × 10(8) RNA-Seq reads were acquired from three stages: hyphal knot (SM), primordium (SP), and primordium differentiation (SPD). The de novo assembly...

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Autores principales: Shu, Lili, Wang, Miaoyue, Xu, Hui, Qiu, Zhiheng, Li, Tianlai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9247108/
https://www.ncbi.nlm.nih.gov/pubmed/35773379
http://dx.doi.org/10.1038/s41598-022-15382-5
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author Shu, Lili
Wang, Miaoyue
Xu, Hui
Qiu, Zhiheng
Li, Tianlai
author_facet Shu, Lili
Wang, Miaoyue
Xu, Hui
Qiu, Zhiheng
Li, Tianlai
author_sort Shu, Lili
collection PubMed
description The genes associated with fruiting body formation of Sparasis latifolia are valuable for improving mushroom breeding. To investigate this process, 4.8 × 10(8) RNA-Seq reads were acquired from three stages: hyphal knot (SM), primordium (SP), and primordium differentiation (SPD). The de novo assembly generated a total of 48,549 unigenes, of which 71.53% (34,728) unigenes could be annotated by at least one of the KEGG (Kyoto Encyclopedia of Genes and Genomes), GO (Gene Ontology), and KOG (Eukaryotic Orthologous Group) databases. KEGG and KOG analyses respectively mapped 32,765 unigenes to 202 pathways and 19,408 unigenes to 25 categories. KEGG pathway enrichment analysis of DEGs (differentially expressed genes) indicated primordium initiation was significantly related to 66 pathways, such as “Ribosome”, “metabolism of xenobiotics by cytochrome P450”, and “glutathione metabolism” (among others). The MAPK and mTOR signal transduction pathways underwent significant adjustments during the SM to SP transition. Further, our research revealed the PI3K-Akt signaling pathway related to cell proliferation could play crucial functions during the development of SP and SPD. These findings provide crucial candidate genes and pathways related to primordium differentiation and development in S. latifolia, and advances our knowledge about mushroom morphogenesis.
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spelling pubmed-92471082022-07-02 De novo transcriptome assembly and comprehensive assessment provide insight into fruiting body formation of Sparassis latifolia Shu, Lili Wang, Miaoyue Xu, Hui Qiu, Zhiheng Li, Tianlai Sci Rep Article The genes associated with fruiting body formation of Sparasis latifolia are valuable for improving mushroom breeding. To investigate this process, 4.8 × 10(8) RNA-Seq reads were acquired from three stages: hyphal knot (SM), primordium (SP), and primordium differentiation (SPD). The de novo assembly generated a total of 48,549 unigenes, of which 71.53% (34,728) unigenes could be annotated by at least one of the KEGG (Kyoto Encyclopedia of Genes and Genomes), GO (Gene Ontology), and KOG (Eukaryotic Orthologous Group) databases. KEGG and KOG analyses respectively mapped 32,765 unigenes to 202 pathways and 19,408 unigenes to 25 categories. KEGG pathway enrichment analysis of DEGs (differentially expressed genes) indicated primordium initiation was significantly related to 66 pathways, such as “Ribosome”, “metabolism of xenobiotics by cytochrome P450”, and “glutathione metabolism” (among others). The MAPK and mTOR signal transduction pathways underwent significant adjustments during the SM to SP transition. Further, our research revealed the PI3K-Akt signaling pathway related to cell proliferation could play crucial functions during the development of SP and SPD. These findings provide crucial candidate genes and pathways related to primordium differentiation and development in S. latifolia, and advances our knowledge about mushroom morphogenesis. Nature Publishing Group UK 2022-06-30 /pmc/articles/PMC9247108/ /pubmed/35773379 http://dx.doi.org/10.1038/s41598-022-15382-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Shu, Lili
Wang, Miaoyue
Xu, Hui
Qiu, Zhiheng
Li, Tianlai
De novo transcriptome assembly and comprehensive assessment provide insight into fruiting body formation of Sparassis latifolia
title De novo transcriptome assembly and comprehensive assessment provide insight into fruiting body formation of Sparassis latifolia
title_full De novo transcriptome assembly and comprehensive assessment provide insight into fruiting body formation of Sparassis latifolia
title_fullStr De novo transcriptome assembly and comprehensive assessment provide insight into fruiting body formation of Sparassis latifolia
title_full_unstemmed De novo transcriptome assembly and comprehensive assessment provide insight into fruiting body formation of Sparassis latifolia
title_short De novo transcriptome assembly and comprehensive assessment provide insight into fruiting body formation of Sparassis latifolia
title_sort de novo transcriptome assembly and comprehensive assessment provide insight into fruiting body formation of sparassis latifolia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9247108/
https://www.ncbi.nlm.nih.gov/pubmed/35773379
http://dx.doi.org/10.1038/s41598-022-15382-5
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