author_facet Li, X.Q.
Guo, B.L.
Cai, W.Y.
Zhang, J.M.
Huang, H.Q.
Zhan, P.
Xi, L.Y.
Vicente, V.A.
Stielow, B.
Sun, J.F.
de Hoog, G.S.
Li, X.Q.
Guo, B.L.
Cai, W.Y.
Zhang, J.M.
Huang, H.Q.
Zhan, P.
Xi, L.Y.
Vicente, V.A.
Stielow, B.
Sun, J.F.
de Hoog, G.S.
author Li, X.Q.
Guo, B.L.
Cai, W.Y.
Zhang, J.M.
Huang, H.Q.
Zhan, P.
Xi, L.Y.
Vicente, V.A.
Stielow, B.
Sun, J.F.
de Hoog, G.S.
spellingShingle Li, X.Q.
Guo, B.L.
Cai, W.Y.
Zhang, J.M.
Huang, H.Q.
Zhan, P.
Xi, L.Y.
Vicente, V.A.
Stielow, B.
Sun, J.F.
de Hoog, G.S.
Studies in Mycology
The role of melanin pathways in extremotolerance and virulence ofFonsecaearevealed byde novoassembly transcriptomics using illumina paired-end sequencing
Agricultural and Biological Sciences (miscellaneous)
author_sort li, x.q.
spelling Li, X.Q. Guo, B.L. Cai, W.Y. Zhang, J.M. Huang, H.Q. Zhan, P. Xi, L.Y. Vicente, V.A. Stielow, B. Sun, J.F. de Hoog, G.S. 0166-0616 Westerdijk Fungal Biodiversity Institute Agricultural and Biological Sciences (miscellaneous) http://dx.doi.org/10.1016/j.simyco.2016.02.001 <jats:p>Melanisation has been considered to be an important virulence factor of<jats:italic>Fonsecaea monophora</jats:italic>. However, the biosynthetic mechanisms of melanisation remain unknown. We therefore used next generation sequencing technology to investigate the transcriptome and digital gene expression data, which are valuable resources to better understand the molecular and biological mechanisms regulating melanisation in<jats:italic>F. monophora</jats:italic>. We performed<jats:italic>de novo</jats:italic>transcriptome assembly and digital gene expression (DGE) profiling analyses of parent (CBS 122845) and albino (CBS 125194) strains using the Illumina RNA-seq system. A total of 17 352 annotated unigenes were found by BLAST search of NR, Swiss-Prot, Gene Ontology, Clusters of Orthologous Groups and Kyoto Encyclopedia of Genes and Genomes (KEGG) (<jats:italic>E</jats:italic>-value &lt;1e‐5). A total of 2 283 unigenes were judged to be the differentially expressed between the two genotypes. We identified most of the genes coding for key enzymes involved in melanin biosynthesis pathways, including polyketide synthase (<jats:italic>pks</jats:italic>), multicopper oxidase (<jats:italic>mco</jats:italic>), laccase, tyrosinase and homogentisate 1,2-dioxygenase (<jats:italic>hmgA</jats:italic>). DEG analysis showed extensive down-regulation of key genes in the DHN pathway, while up-regulation was noted in the DOPA pathway of the albino mutant. The transcript levels of partial genes were confirmed by real time RT-PCR, while the crucial role of key enzymes was confirmed by either inhibitor or substrate tests<jats:italic>in vitro</jats:italic>. Meanwhile, numbers of genes involved in light sensing, cell wall synthesis, morphology and environmental stress were identified in the transcriptome of<jats:italic>F. monophora</jats:italic>. In addition, 3 353 SSRs (Simple Sequence Repeats) markers were identified from 21 600 consensus sequences. Blocking of the DNH pathway is the most likely reason of melanin deficiency in the albino strain, while the production of pheomelanin and pyomelanin were probably regulated by unknown transcription factors on upstream of both pathways. Most of genes involved in environmental tolerance to oxidants, irradiation and extreme temperatures were also assembled and annotated in transcriptomes of<jats:italic>F. monophora</jats:italic>. In addition, thousands of identified cSSR (combined SSR) markers will favour further genetic linkage studies. In conclusion, these data will contribute to understanding the regulation of melanin biosynthesis and help to improve the studies of pathogenicity of<jats:italic>F. monophora</jats:italic>.</jats:p> The role of melanin pathways in extremotolerance and virulence of<i>Fonsecaea</i>revealed by<i>de novo</i>assembly transcriptomics using illumina paired-end sequencing Studies in Mycology
doi_str_mv 10.1016/j.simyco.2016.02.001
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publishDateSort 2016
publisher Westerdijk Fungal Biodiversity Institute
recordtype ai
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series Studies in Mycology
source_id 49
title The role of melanin pathways in extremotolerance and virulence ofFonsecaearevealed byde novoassembly transcriptomics using illumina paired-end sequencing
title_unstemmed The role of melanin pathways in extremotolerance and virulence ofFonsecaearevealed byde novoassembly transcriptomics using illumina paired-end sequencing
title_full The role of melanin pathways in extremotolerance and virulence ofFonsecaearevealed byde novoassembly transcriptomics using illumina paired-end sequencing
title_fullStr The role of melanin pathways in extremotolerance and virulence ofFonsecaearevealed byde novoassembly transcriptomics using illumina paired-end sequencing
title_full_unstemmed The role of melanin pathways in extremotolerance and virulence ofFonsecaearevealed byde novoassembly transcriptomics using illumina paired-end sequencing
title_short The role of melanin pathways in extremotolerance and virulence ofFonsecaearevealed byde novoassembly transcriptomics using illumina paired-end sequencing
title_sort the role of melanin pathways in extremotolerance and virulence of<i>fonsecaea</i>revealed by<i>de novo</i>assembly transcriptomics using illumina paired-end sequencing
topic Agricultural and Biological Sciences (miscellaneous)
url http://dx.doi.org/10.1016/j.simyco.2016.02.001
publishDate 2016
physical 1-18
description <jats:p>Melanisation has been considered to be an important virulence factor of<jats:italic>Fonsecaea monophora</jats:italic>. However, the biosynthetic mechanisms of melanisation remain unknown. We therefore used next generation sequencing technology to investigate the transcriptome and digital gene expression data, which are valuable resources to better understand the molecular and biological mechanisms regulating melanisation in<jats:italic>F. monophora</jats:italic>. We performed<jats:italic>de novo</jats:italic>transcriptome assembly and digital gene expression (DGE) profiling analyses of parent (CBS 122845) and albino (CBS 125194) strains using the Illumina RNA-seq system. A total of 17 352 annotated unigenes were found by BLAST search of NR, Swiss-Prot, Gene Ontology, Clusters of Orthologous Groups and Kyoto Encyclopedia of Genes and Genomes (KEGG) (<jats:italic>E</jats:italic>-value &lt;1e‐5). A total of 2 283 unigenes were judged to be the differentially expressed between the two genotypes. We identified most of the genes coding for key enzymes involved in melanin biosynthesis pathways, including polyketide synthase (<jats:italic>pks</jats:italic>), multicopper oxidase (<jats:italic>mco</jats:italic>), laccase, tyrosinase and homogentisate 1,2-dioxygenase (<jats:italic>hmgA</jats:italic>). DEG analysis showed extensive down-regulation of key genes in the DHN pathway, while up-regulation was noted in the DOPA pathway of the albino mutant. The transcript levels of partial genes were confirmed by real time RT-PCR, while the crucial role of key enzymes was confirmed by either inhibitor or substrate tests<jats:italic>in vitro</jats:italic>. Meanwhile, numbers of genes involved in light sensing, cell wall synthesis, morphology and environmental stress were identified in the transcriptome of<jats:italic>F. monophora</jats:italic>. In addition, 3 353 SSRs (Simple Sequence Repeats) markers were identified from 21 600 consensus sequences. Blocking of the DNH pathway is the most likely reason of melanin deficiency in the albino strain, while the production of pheomelanin and pyomelanin were probably regulated by unknown transcription factors on upstream of both pathways. Most of genes involved in environmental tolerance to oxidants, irradiation and extreme temperatures were also assembled and annotated in transcriptomes of<jats:italic>F. monophora</jats:italic>. In addition, thousands of identified cSSR (combined SSR) markers will favour further genetic linkage studies. In conclusion, these data will contribute to understanding the regulation of melanin biosynthesis and help to improve the studies of pathogenicity of<jats:italic>F. monophora</jats:italic>.</jats:p>
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author Li, X.Q., Guo, B.L., Cai, W.Y., Zhang, J.M., Huang, H.Q., Zhan, P., Xi, L.Y., Vicente, V.A., Stielow, B., Sun, J.F., de Hoog, G.S.
author_facet Li, X.Q., Guo, B.L., Cai, W.Y., Zhang, J.M., Huang, H.Q., Zhan, P., Xi, L.Y., Vicente, V.A., Stielow, B., Sun, J.F., de Hoog, G.S., Li, X.Q., Guo, B.L., Cai, W.Y., Zhang, J.M., Huang, H.Q., Zhan, P., Xi, L.Y., Vicente, V.A., Stielow, B., Sun, J.F., de Hoog, G.S.
author_sort li, x.q.
container_issue 1
container_start_page 1
container_title Studies in Mycology
container_volume 83
description <jats:p>Melanisation has been considered to be an important virulence factor of<jats:italic>Fonsecaea monophora</jats:italic>. However, the biosynthetic mechanisms of melanisation remain unknown. We therefore used next generation sequencing technology to investigate the transcriptome and digital gene expression data, which are valuable resources to better understand the molecular and biological mechanisms regulating melanisation in<jats:italic>F. monophora</jats:italic>. We performed<jats:italic>de novo</jats:italic>transcriptome assembly and digital gene expression (DGE) profiling analyses of parent (CBS 122845) and albino (CBS 125194) strains using the Illumina RNA-seq system. A total of 17 352 annotated unigenes were found by BLAST search of NR, Swiss-Prot, Gene Ontology, Clusters of Orthologous Groups and Kyoto Encyclopedia of Genes and Genomes (KEGG) (<jats:italic>E</jats:italic>-value &lt;1e‐5). A total of 2 283 unigenes were judged to be the differentially expressed between the two genotypes. We identified most of the genes coding for key enzymes involved in melanin biosynthesis pathways, including polyketide synthase (<jats:italic>pks</jats:italic>), multicopper oxidase (<jats:italic>mco</jats:italic>), laccase, tyrosinase and homogentisate 1,2-dioxygenase (<jats:italic>hmgA</jats:italic>). DEG analysis showed extensive down-regulation of key genes in the DHN pathway, while up-regulation was noted in the DOPA pathway of the albino mutant. The transcript levels of partial genes were confirmed by real time RT-PCR, while the crucial role of key enzymes was confirmed by either inhibitor or substrate tests<jats:italic>in vitro</jats:italic>. Meanwhile, numbers of genes involved in light sensing, cell wall synthesis, morphology and environmental stress were identified in the transcriptome of<jats:italic>F. monophora</jats:italic>. In addition, 3 353 SSRs (Simple Sequence Repeats) markers were identified from 21 600 consensus sequences. Blocking of the DNH pathway is the most likely reason of melanin deficiency in the albino strain, while the production of pheomelanin and pyomelanin were probably regulated by unknown transcription factors on upstream of both pathways. Most of genes involved in environmental tolerance to oxidants, irradiation and extreme temperatures were also assembled and annotated in transcriptomes of<jats:italic>F. monophora</jats:italic>. In addition, thousands of identified cSSR (combined SSR) markers will favour further genetic linkage studies. In conclusion, these data will contribute to understanding the regulation of melanin biosynthesis and help to improve the studies of pathogenicity of<jats:italic>F. monophora</jats:italic>.</jats:p>
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spelling Li, X.Q. Guo, B.L. Cai, W.Y. Zhang, J.M. Huang, H.Q. Zhan, P. Xi, L.Y. Vicente, V.A. Stielow, B. Sun, J.F. de Hoog, G.S. 0166-0616 Westerdijk Fungal Biodiversity Institute Agricultural and Biological Sciences (miscellaneous) http://dx.doi.org/10.1016/j.simyco.2016.02.001 <jats:p>Melanisation has been considered to be an important virulence factor of<jats:italic>Fonsecaea monophora</jats:italic>. However, the biosynthetic mechanisms of melanisation remain unknown. We therefore used next generation sequencing technology to investigate the transcriptome and digital gene expression data, which are valuable resources to better understand the molecular and biological mechanisms regulating melanisation in<jats:italic>F. monophora</jats:italic>. We performed<jats:italic>de novo</jats:italic>transcriptome assembly and digital gene expression (DGE) profiling analyses of parent (CBS 122845) and albino (CBS 125194) strains using the Illumina RNA-seq system. A total of 17 352 annotated unigenes were found by BLAST search of NR, Swiss-Prot, Gene Ontology, Clusters of Orthologous Groups and Kyoto Encyclopedia of Genes and Genomes (KEGG) (<jats:italic>E</jats:italic>-value &lt;1e‐5). A total of 2 283 unigenes were judged to be the differentially expressed between the two genotypes. We identified most of the genes coding for key enzymes involved in melanin biosynthesis pathways, including polyketide synthase (<jats:italic>pks</jats:italic>), multicopper oxidase (<jats:italic>mco</jats:italic>), laccase, tyrosinase and homogentisate 1,2-dioxygenase (<jats:italic>hmgA</jats:italic>). DEG analysis showed extensive down-regulation of key genes in the DHN pathway, while up-regulation was noted in the DOPA pathway of the albino mutant. The transcript levels of partial genes were confirmed by real time RT-PCR, while the crucial role of key enzymes was confirmed by either inhibitor or substrate tests<jats:italic>in vitro</jats:italic>. Meanwhile, numbers of genes involved in light sensing, cell wall synthesis, morphology and environmental stress were identified in the transcriptome of<jats:italic>F. monophora</jats:italic>. In addition, 3 353 SSRs (Simple Sequence Repeats) markers were identified from 21 600 consensus sequences. Blocking of the DNH pathway is the most likely reason of melanin deficiency in the albino strain, while the production of pheomelanin and pyomelanin were probably regulated by unknown transcription factors on upstream of both pathways. Most of genes involved in environmental tolerance to oxidants, irradiation and extreme temperatures were also assembled and annotated in transcriptomes of<jats:italic>F. monophora</jats:italic>. In addition, thousands of identified cSSR (combined SSR) markers will favour further genetic linkage studies. In conclusion, these data will contribute to understanding the regulation of melanin biosynthesis and help to improve the studies of pathogenicity of<jats:italic>F. monophora</jats:italic>.</jats:p> The role of melanin pathways in extremotolerance and virulence of<i>Fonsecaea</i>revealed by<i>de novo</i>assembly transcriptomics using illumina paired-end sequencing Studies in Mycology
spellingShingle Li, X.Q., Guo, B.L., Cai, W.Y., Zhang, J.M., Huang, H.Q., Zhan, P., Xi, L.Y., Vicente, V.A., Stielow, B., Sun, J.F., de Hoog, G.S., Studies in Mycology, The role of melanin pathways in extremotolerance and virulence ofFonsecaearevealed byde novoassembly transcriptomics using illumina paired-end sequencing, Agricultural and Biological Sciences (miscellaneous)
title The role of melanin pathways in extremotolerance and virulence ofFonsecaearevealed byde novoassembly transcriptomics using illumina paired-end sequencing
title_full The role of melanin pathways in extremotolerance and virulence ofFonsecaearevealed byde novoassembly transcriptomics using illumina paired-end sequencing
title_fullStr The role of melanin pathways in extremotolerance and virulence ofFonsecaearevealed byde novoassembly transcriptomics using illumina paired-end sequencing
title_full_unstemmed The role of melanin pathways in extremotolerance and virulence ofFonsecaearevealed byde novoassembly transcriptomics using illumina paired-end sequencing
title_short The role of melanin pathways in extremotolerance and virulence ofFonsecaearevealed byde novoassembly transcriptomics using illumina paired-end sequencing
title_sort the role of melanin pathways in extremotolerance and virulence of<i>fonsecaea</i>revealed by<i>de novo</i>assembly transcriptomics using illumina paired-end sequencing
title_unstemmed The role of melanin pathways in extremotolerance and virulence ofFonsecaearevealed byde novoassembly transcriptomics using illumina paired-end sequencing
topic Agricultural and Biological Sciences (miscellaneous)
url http://dx.doi.org/10.1016/j.simyco.2016.02.001