Genome assembly, annotation and comparative analysis of the maize fungal pathogen Cercospora zeina

dc.contributor.advisorReva, Oleg N.
dc.contributor.coadvisorBerger, David Kenneth
dc.contributor.emailnicky.olivier@up.ac.zaen_US
dc.contributor.postgraduateOlivier, Nicholas Abraham
dc.date.accessioned2024-08-26T12:44:34Z
dc.date.available2024-08-26T12:44:34Z
dc.date.created2020-04
dc.date.issued2019-06
dc.descriptionThesis (PhD (Bioinformatics))--University of Pretoria, 2019.en_US
dc.description.abstractThe fungal pathogen Cercospora zeina causes Grey leaf spot (GLS), a devastating yield-limiting foliar disease of maize. GLS negatively impacts food security, especially in sub-Saharan Africa where maize is a staple food source. In this study the genomic DNA of C. zeina was sequenced using next-generation sequencing, and the genome assembled to a 95.4% completeness based on the presence of core genes. The functionality of the genome was confirmed by transcriptome sequencing data mapping to the genome. Phylogenetics analysis confirmed the genome to cluster with other C. zeina isolates. The functional elements and gene regions were predicted using the MAKER genome annotation pipeline. The predicted proteins were compared with the closely related species Cercospora zeae-maydis, Cercospora beticola and Cercospora berteroae. Functional annotation of proteins of specific classes were performed to identify differences in secreted proteins, carbohydrate-active enzymes, lipases, proteases and components of secondary metabolite biosynthesis clusters. The synteny of the genes in the cercosporin toxin biosynthesis cluster was also confirmed in all four species. To enhance the accuracy of the phylogenetic classification of Cercospora species the orthologous relationship between proteins of a number of Dothideomycete species were predicted. The single-copy orthologs specific to the Cercospora genus were analyzed for phylogenetic information content, and eight genes selected for primer design in regions of protein identity. Primers for four genes were synthesized and tested for specificity during amplification of C. zeina and C. zeae-maydis genomic DNA. Degenerate primer pairs for two genes were selected for further analysis, due to sequencing confirming the correct identity of the amplification products.en_US
dc.description.availabilityUnrestricteden_US
dc.description.degreePhD (Bioinformatics)en_US
dc.description.departmentBiochemistryen_US
dc.description.facultyFaculty of Natural and Agricultural Sciencesen_US
dc.identifier.citation*en_US
dc.identifier.otherA2020en_US
dc.identifier.urihttp://hdl.handle.net/2263/97868
dc.language.isoenen_US
dc.publisherUniversity of Pretoria
dc.rights© 2021 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria.
dc.subjectUCTDen_US
dc.titleGenome assembly, annotation and comparative analysis of the maize fungal pathogen Cercospora zeinaen_US
dc.typeThesisen_US

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