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Dynamics of the Phanerochaete carnosa transcriptome during growth on aspen and spruce.

Identifieur interne : 000F46 ( Main/Exploration ); précédent : 000F45; suivant : 000F47

Dynamics of the Phanerochaete carnosa transcriptome during growth on aspen and spruce.

Auteurs : E. Jurak [Finlande, Pays-Bas] ; H. Suzuki [Canada] ; G. Van Erven [Pays-Bas] ; J A Gandier [Canada] ; P. Wong [Canada] ; K. Chan [Canada] ; C Y Ho [Canada] ; Y. Gong [Canada] ; E. Tillier [Canada] ; M-N Rosso [France] ; M A Kabel [Pays-Bas] ; S. Miyauchi [France] ; E R Master [Finlande, Canada]

Source :

RBID : pubmed:30424733

Descripteurs français

English descriptors

Abstract

BACKGROUND

The basidiomycete Phanerochaete carnosa is a white-rot species that has been mainly isolated from coniferous softwood. Given the particular recalcitrance of softwoods to bioconversion, we conducted a comparative transcriptomic analysis of P. carnosa following growth on wood powder from one softwood (spruce; Picea glauca) and one hardwood (aspen; Populus tremuloides). P. carnosa was grown on each substrate for over one month, and mycelia were harvested at five time points for total RNA sequencing. Residual wood powder was also analyzed for total sugar and lignin composition.

RESULTS

Following a slightly longer lag phase of growth on spruce, radial expansion of the P. carnosa colony was similar on spruce and aspen. Consistent with this observation, the pattern of gene expression by P. carnosa on each substrate converged following the initial adaptation. On both substrates, highest transcript abundances were attributed to genes predicted to encode manganese peroxidases (MnP), along with auxiliary activities from carbohydrate-active enzyme (CAZy) families AA3 and AA5. In addition, a lytic polysaccharide monooxygenase from family AA9 was steadily expressed throughout growth on both substrates. P450 sequences from clans CPY52 and CYP64 accounted for 50% or more of the most highly expressed P450s, which were also the P450 clans that were expanded in the P. carnosa genome relative to other white-rot fungi.

CONCLUSIONS

The inclusion of five growth points and two wood substrates was important to revealing differences in the expression profiles of specific sequences within large glycoside hydrolase families (e.g., GH5 and GH16), and permitted co-expression analyses that identified new targets for study, including non-catalytic proteins and proteins with unknown function.


DOI: 10.1186/s12864-018-5210-z
PubMed: 30424733
PubMed Central: PMC6234650


Affiliations:


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<title level="j">BMC genomics</title>
<idno type="eISSN">1471-2164</idno>
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<date when="2018" type="published">2018</date>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Fungal Proteins (genetics)</term>
<term>Gene Expression Profiling (MeSH)</term>
<term>Gene Expression Regulation, Fungal (MeSH)</term>
<term>Phanerochaete (genetics)</term>
<term>Phanerochaete (physiology)</term>
<term>Picea (microbiology)</term>
<term>Populus (microbiology)</term>
<term>Transcriptome (MeSH)</term>
<term>Wood (microbiology)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Analyse de profil d'expression de gènes (MeSH)</term>
<term>Bois (microbiologie)</term>
<term>Phanerochaete (génétique)</term>
<term>Phanerochaete (physiologie)</term>
<term>Picea (microbiologie)</term>
<term>Populus (microbiologie)</term>
<term>Protéines fongiques (génétique)</term>
<term>Régulation de l'expression des gènes fongiques (MeSH)</term>
<term>Transcriptome (MeSH)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>Fungal Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Phanerochaete</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Phanerochaete</term>
<term>Protéines fongiques</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr">
<term>Bois</term>
<term>Picea</term>
<term>Populus</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiology" xml:lang="en">
<term>Picea</term>
<term>Populus</term>
<term>Wood</term>
</keywords>
<keywords scheme="MESH" qualifier="physiologie" xml:lang="fr">
<term>Phanerochaete</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en">
<term>Phanerochaete</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Gene Expression Profiling</term>
<term>Gene Expression Regulation, Fungal</term>
<term>Transcriptome</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Analyse de profil d'expression de gènes</term>
<term>Régulation de l'expression des gènes fongiques</term>
<term>Transcriptome</term>
</keywords>
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<front>
<div type="abstract" xml:lang="en">
<p>
<b>BACKGROUND</b>
</p>
<p>The basidiomycete Phanerochaete carnosa is a white-rot species that has been mainly isolated from coniferous softwood. Given the particular recalcitrance of softwoods to bioconversion, we conducted a comparative transcriptomic analysis of P. carnosa following growth on wood powder from one softwood (spruce; Picea glauca) and one hardwood (aspen; Populus tremuloides). P. carnosa was grown on each substrate for over one month, and mycelia were harvested at five time points for total RNA sequencing. Residual wood powder was also analyzed for total sugar and lignin composition.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>Following a slightly longer lag phase of growth on spruce, radial expansion of the P. carnosa colony was similar on spruce and aspen. Consistent with this observation, the pattern of gene expression by P. carnosa on each substrate converged following the initial adaptation. On both substrates, highest transcript abundances were attributed to genes predicted to encode manganese peroxidases (MnP), along with auxiliary activities from carbohydrate-active enzyme (CAZy) families AA3 and AA5. In addition, a lytic polysaccharide monooxygenase from family AA9 was steadily expressed throughout growth on both substrates. P450 sequences from clans CPY52 and CYP64 accounted for 50% or more of the most highly expressed P450s, which were also the P450 clans that were expanded in the P. carnosa genome relative to other white-rot fungi.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS</b>
</p>
<p>The inclusion of five growth points and two wood substrates was important to revealing differences in the expression profiles of specific sequences within large glycoside hydrolase families (e.g., GH5 and GH16), and permitted co-expression analyses that identified new targets for study, including non-catalytic proteins and proteins with unknown function.</p>
</div>
</front>
</TEI>
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<DateCompleted>
<Year>2019</Year>
<Month>02</Month>
<Day>06</Day>
</DateCompleted>
<DateRevised>
<Year>2019</Year>
<Month>02</Month>
<Day>15</Day>
</DateRevised>
<Article PubModel="Electronic">
<Journal>
<ISSN IssnType="Electronic">1471-2164</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>19</Volume>
<Issue>1</Issue>
<PubDate>
<Year>2018</Year>
<Month>Nov</Month>
<Day>13</Day>
</PubDate>
</JournalIssue>
<Title>BMC genomics</Title>
<ISOAbbreviation>BMC Genomics</ISOAbbreviation>
</Journal>
<ArticleTitle>Dynamics of the Phanerochaete carnosa transcriptome during growth on aspen and spruce.</ArticleTitle>
<Pagination>
<MedlinePgn>815</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1186/s12864-018-5210-z</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">The basidiomycete Phanerochaete carnosa is a white-rot species that has been mainly isolated from coniferous softwood. Given the particular recalcitrance of softwoods to bioconversion, we conducted a comparative transcriptomic analysis of P. carnosa following growth on wood powder from one softwood (spruce; Picea glauca) and one hardwood (aspen; Populus tremuloides). P. carnosa was grown on each substrate for over one month, and mycelia were harvested at five time points for total RNA sequencing. Residual wood powder was also analyzed for total sugar and lignin composition.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Following a slightly longer lag phase of growth on spruce, radial expansion of the P. carnosa colony was similar on spruce and aspen. Consistent with this observation, the pattern of gene expression by P. carnosa on each substrate converged following the initial adaptation. On both substrates, highest transcript abundances were attributed to genes predicted to encode manganese peroxidases (MnP), along with auxiliary activities from carbohydrate-active enzyme (CAZy) families AA3 and AA5. In addition, a lytic polysaccharide monooxygenase from family AA9 was steadily expressed throughout growth on both substrates. P450 sequences from clans CPY52 and CYP64 accounted for 50% or more of the most highly expressed P450s, which were also the P450 clans that were expanded in the P. carnosa genome relative to other white-rot fungi.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">The inclusion of five growth points and two wood substrates was important to revealing differences in the expression profiles of specific sequences within large glycoside hydrolase families (e.g., GH5 and GH16), and permitted co-expression analyses that identified new targets for study, including non-catalytic proteins and proteins with unknown function.</AbstractText>
</Abstract>
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<Author ValidYN="Y">
<LastName>Jurak</LastName>
<ForeName>E</ForeName>
<Initials>E</Initials>
<AffiliationInfo>
<Affiliation>Department of Bioproducts and Biosystems, Aalto University, Espoo, Finland.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Aquatic Biotechnology and Bioproduct Engineering, Groningen, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Suzuki</LastName>
<ForeName>H</ForeName>
<Initials>H</Initials>
<AffiliationInfo>
<Affiliation>Department of Chemical Engineering and Applied Chemistry, University of Toronto, Toronto, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>van Erven</LastName>
<ForeName>G</ForeName>
<Initials>G</Initials>
<AffiliationInfo>
<Affiliation>Wageningen University, Laboratory of Food Chemistry, Bornse Weilanden 9, 6708, WG, Wageningen, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Gandier</LastName>
<ForeName>J A</ForeName>
<Initials>JA</Initials>
<AffiliationInfo>
<Affiliation>Department of Chemical Engineering and Applied Chemistry, University of Toronto, Toronto, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Wong</LastName>
<ForeName>P</ForeName>
<Initials>P</Initials>
<AffiliationInfo>
<Affiliation>Department of Medical Biophysics, University of Toronto, Toronto, Canada.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Chan</LastName>
<ForeName>K</ForeName>
<Initials>K</Initials>
<AffiliationInfo>
<Affiliation>Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Ho</LastName>
<ForeName>C Y</ForeName>
<Initials>CY</Initials>
<AffiliationInfo>
<Affiliation>Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Gong</LastName>
<ForeName>Y</ForeName>
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<AffiliationInfo>
<Affiliation>Centre for the Analysis of Genome Evolution and Function, University of Toronto, Toronto, Canada.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y">
<LastName>Tillier</LastName>
<ForeName>E</ForeName>
<Initials>E</Initials>
<AffiliationInfo>
<Affiliation>Department of Medical Biophysics, University of Toronto, Toronto, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Rosso</LastName>
<ForeName>M-N</ForeName>
<Initials>MN</Initials>
<AffiliationInfo>
<Affiliation>Aix-Marseille Université, INRA, UMR1163, Biodiversité et Biotechnologie Fongiques, Marseille, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Kabel</LastName>
<ForeName>M A</ForeName>
<Initials>MA</Initials>
<AffiliationInfo>
<Affiliation>Wageningen University, Laboratory of Food Chemistry, Bornse Weilanden 9, 6708, WG, Wageningen, The Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Miyauchi</LastName>
<ForeName>S</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>Laboratory of Excellence ARBRE, INRA, Nancy, Lorraine, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Aix-Marseille Université, INRA, UMR1163, Biodiversité et Biotechnologie Fongiques, Marseille, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Master</LastName>
<ForeName>E R</ForeName>
<Initials>ER</Initials>
<AffiliationInfo>
<Affiliation>Department of Bioproducts and Biosystems, Aalto University, Espoo, Finland. emma.master@utoronto.ca.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Chemical Engineering and Applied Chemistry, University of Toronto, Toronto, Canada. emma.master@utoronto.ca.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<GrantList CompleteYN="Y">
<Grant>
<GrantID>ORF-RE-05-005</GrantID>
<Agency>Government of Ontario</Agency>
<Country></Country>
</Grant>
<Grant>
<GrantID>648925</GrantID>
<Agency>European Research Council</Agency>
<Country>International</Country>
</Grant>
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<Year>2018</Year>
<Month>11</Month>
<Day>13</Day>
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<MeshHeading>
<DescriptorName UI="D020869" MajorTopicYN="N">Gene Expression Profiling</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D020075" MajorTopicYN="N">Phanerochaete</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
<QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName>
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<MeshHeading>
<DescriptorName UI="D028222" MajorTopicYN="N">Picea</DescriptorName>
<QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName>
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<MeshHeading>
<DescriptorName UI="D032107" MajorTopicYN="N">Populus</DescriptorName>
<QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName>
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<MeshHeading>
<DescriptorName UI="D059467" MajorTopicYN="Y">Transcriptome</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D014934" MajorTopicYN="N">Wood</DescriptorName>
<QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName>
</MeshHeading>
</MeshHeadingList>
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<Keyword MajorTopicYN="N">Carbohydrate active enzymes</Keyword>
<Keyword MajorTopicYN="N">Hydrophobins</Keyword>
<Keyword MajorTopicYN="N">Lignocellulose conversions</Keyword>
<Keyword MajorTopicYN="N">Loosenins</Keyword>
<Keyword MajorTopicYN="N">Phanerochaete carnosa</Keyword>
<Keyword MajorTopicYN="N">Transcriptomics</Keyword>
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<li>Université Aalto</li>
<li>Université d'Aix-Marseille</li>
<li>Université de Toronto</li>
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<name sortKey="Jurak, E" sort="Jurak, E" uniqKey="Jurak E" first="E" last="Jurak">E. Jurak</name>
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<name sortKey="Master, E R" sort="Master, E R" uniqKey="Master E" first="E R" last="Master">E R Master</name>
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<country name="Pays-Bas">
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<name sortKey="Jurak, E" sort="Jurak, E" uniqKey="Jurak E" first="E" last="Jurak">E. Jurak</name>
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<name sortKey="Kabel, M A" sort="Kabel, M A" uniqKey="Kabel M" first="M A" last="Kabel">M A Kabel</name>
<name sortKey="Van Erven, G" sort="Van Erven, G" uniqKey="Van Erven G" first="G" last="Van Erven">G. Van Erven</name>
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<name sortKey="Suzuki, H" sort="Suzuki, H" uniqKey="Suzuki H" first="H" last="Suzuki">H. Suzuki</name>
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<name sortKey="Chan, K" sort="Chan, K" uniqKey="Chan K" first="K" last="Chan">K. Chan</name>
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<name sortKey="Wong, P" sort="Wong, P" uniqKey="Wong P" first="P" last="Wong">P. Wong</name>
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