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dc.contributor.authorAntonieto, ACC
dc.contributor.authorNogueira, KMV
dc.contributor.authorde Paula, RG
dc.contributor.authorNora, LC
dc.contributor.authorCassiano, MHA
dc.contributor.authorGuazzaroni, M-E
dc.contributor.authorAlmeida, F
dc.contributor.authorda Silva, TA
dc.contributor.authorRies, LNA
dc.contributor.authorde Assis, LJ
dc.contributor.authorGoldman, GH
dc.contributor.authorSilva, RN
dc.contributor.authorSilva-Rocha, R
dc.contributor.editorVickers C
dc.date.accessioned2024-02-27T13:46:39Z
dc.date.available2024-02-27T13:46:39Z
dc.date.issued2019-08-27
dc.identifier.issn2379-5077
dc.identifier.issn2379-5077
dc.identifier.otherARTN e00161-19
dc.identifier.urihttps://pearl.plymouth.ac.uk/handle/10026.1/22094
dc.description.abstract

<jats:p> In this work, we used a systems biology approach to map new regulatory interactions in <jats:named-content content-type="genus-species">Trichoderma reesei</jats:named-content> controlling the expression of genes encoding cellulase and hemicellulase. By integrating transcriptomics related to complex biomass degradation, we were able to identify a novel transcriptional regulator which is able to activate the expression of these genes in response to two different cellulose sources. <jats:italic>In vivo</jats:italic> experimental validation confirmed the role of this new regulator in several other processes related to carbon source utilization and nutrient transport. Therefore, this work revealed novel forms of regulatory interaction in this model system for plant biomass deconstruction and also represented a new approach that could be easy applied to other organisms. </jats:p>

dc.format.extente00161-e00119
dc.format.mediumElectronic
dc.languageen
dc.publisherAmerican Society for Microbiology
dc.subjectcis-regulatory elements
dc.subjectholocellulase expression
dc.subjectregulatory networks
dc.subjectsystems biology
dc.titleA Novel Cys2His2 Zinc Finger Homolog of AZF1 Modulates Holocellulase Expression in <i>Trichoderma reesei</i>
dc.typejournal-article
dc.typeArticle
plymouth.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/31213522
plymouth.issue4
plymouth.volume4
plymouth.publisher-urlhttp://dx.doi.org/10.1128/msystems.00161-19
plymouth.publication-statusPublished
plymouth.journalmSystems
dc.identifier.doi10.1128/msystems.00161-19
plymouth.organisational-group|Plymouth
plymouth.organisational-group|Plymouth|Faculty of Health
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA
plymouth.organisational-group|Plymouth|Users by role
plymouth.organisational-group|Plymouth|Users by role|Academics
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA|UoA01 Clinical Medicine
plymouth.organisational-group|Plymouth|Faculty of Health|Peninsula Medical School
plymouth.organisational-group|Plymouth|Faculty of Health|School of Biomedical Sciences
plymouth.organisational-group|Plymouth|REF 2028 Researchers by UoA
plymouth.organisational-group|Plymouth|REF 2028 Researchers by UoA|UoA01 Clinical Medicine
dc.publisher.placeUnited States
dc.date.updated2024-02-27T13:46:38Z
dc.identifier.eissn2379-5077
dc.rights.embargoperiodforever
rioxxterms.versionofrecord10.1128/msystems.00161-19


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