Literature DB >> 28314725

Lentinula edodes Genome Survey and Postharvest Transcriptome Analysis.

Yuichi Sakamoto1, Keiko Nakade2, Shiho Sato2, Kentaro Yoshida2, Kazuhiro Miyazaki3, Satoshi Natsume2, Naotake Konno2.   

Abstract

Lentinula edodes is a popular, cultivated edible and medicinal mushroom. Lentinula edodes is susceptible to postharvest problems, such as gill browning, fruiting body softening, and lentinan degradation. We constructed a de novo assembly draft genome sequence and performed gene prediction for Lentinula edodesDe novo assembly was carried out using short reads from paired-end and mate-paired libraries and by using long reads by PacBio, resulting in a contig number of 1,951 and an N50 of 1 Mb. Furthermore, we predicted genes by Augustus using transcriptome sequencing (RNA-seq) data from the whole life cycle of Lentinula edodes, resulting in 12,959 predicted genes. This analysis revealed that Lentinula edodes lacks lignin peroxidase. To reveal genes involved in the loss of quality of Lentinula edodes postharvest fruiting bodies, transcriptome analysis was carried out using serial analysis of gene expression (SuperSAGE). This analysis revealed that many cell wall-related enzymes are upregulated after harvest, such as β-1,3-1,6-glucan-degrading enzymes in glycoside hydrolase (GH) families GH5, GH16, GH30, GH55, and GH128, and thaumatin-like proteins. In addition, we found that several chitin-related genes are upregulated, such as putative chitinases in GH family 18, exochitinases in GH20, and a putative chitosanase in GH family 75. The results suggest that cell wall-degrading enzymes synergistically cooperate for rapid fruiting body autolysis. Many putative transcription factor genes were upregulated postharvest, such as genes containing high-mobility-group (HMG) domains and zinc finger domains. Several cell death-related proteins were also upregulated postharvest.IMPORTANCE Our data collectively suggest that there is a rapid fruiting body autolysis system in Lentinula edodes The genes for the loss of postharvest quality newly found in this research will be targets for the future breeding of strains that keep fresh longer than present strains. De novoLentinula edodes genome assembly data will be used for the construction of a complete Lentinula edodes chromosome map for future breeding.
Copyright © 2017 American Society for Microbiology.

Entities:  

Keywords:  chitin; fruiting body; glucan; lentinan; senescence

Mesh:

Substances:

Year:  2017        PMID: 28314725      PMCID: PMC5411510          DOI: 10.1128/AEM.02990-16

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  76 in total

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Journal:  Fungal Genet Biol       Date:  2007-11-28       Impact factor: 3.495

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Authors:  Diego Martinez; Luis F Larrondo; Nik Putnam; Maarten D Sollewijn Gelpke; Katherine Huang; Jarrod Chapman; Kevin G Helfenbein; Preethi Ramaiya; J Chris Detter; Frank Larimer; Pedro M Coutinho; Bernard Henrissat; Randy Berka; Dan Cullen; Daniel Rokhsar
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10.  Gene expression studies of the dikaryotic mycelium and primordium of Lentinula edodes by serial analysis of gene expression.

Authors:  Winnie Wing Yan Chum; Kevin Tak Pan Ng; Rita Sheung Mei Shih; Chun Hang Au; Hoi Shan Kwan
Journal:  Mycol Res       Date:  2008-03-25
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5.  Genetically Independent Tetranucleotide to Hexanucleotide Core Motif SSR Markers for Identifying Lentinula edodes Cultivars.

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7.  Comparative transcriptome analysis of dikaryotic mycelia and mature fruiting bodies in the edible mushroom Lentinula edodes.

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8.  Transcriptome analysis of the edible mushroom Lentinula edodes in response to blue light.

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9.  Expression Profile of Laccase Gene Family in White-Rot Basidiomycete Lentinula edodes under Different Environmental Stresses.

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Journal:  Genes (Basel)       Date:  2019-12-16       Impact factor: 4.096

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