Haplotype-resolved genome assembly of an F1 hybrid of Eucalyptus urophylla x E. grandis

dc.contributor.advisorMyburg, Alexander Andrew
dc.contributor.coadvisorDuong, Tuan A.
dc.contributor.coadvisorMizrachi, Eshchar
dc.contributor.coadvisorWegrzyn, Jill L.
dc.contributor.emailanneri.lotter@fabi.up.ac.zaen_ZA
dc.contributor.postgraduateLötter, Anneri
dc.date.accessioned2022-02-14T08:47:26Z
dc.date.available2022-02-14T08:47:26Z
dc.date.created2022-04
dc.date.issued2021
dc.descriptionDissertation (MSc (Genetics))--University of Pretoria, 2021.en_ZA
dc.description.abstractDe novo haplotype phased genome assemblies based on long-read sequencing technologies have improved the detection and characterization of structural variants (SVs) in plant and animal genomes. As long-reads are able to span across haplotypes, they also allow phased (haplo) assemblies of highly heterozygous genomes such as those of forest trees. Knowledge of SV function and their resulting impact on gene expression can be used by breeders to guide tree improvement. Eucalyptus species and hybrids are some of the most widely planted hardwood trees. Hybrids are often preferred as they combine the genetic background of two species to produce more resilient trees that can inhabit a wider environmental deployment range. For example, E. urophylla x E. grandis hybrids combines disease resistance of E. urophylla with fast growth and desirable wood properties of E. grandis. However, to use such a strategy in eucalypt breeding firstly requires a high-quality reference genome (preferably phased) with which additional de novo assembled genomes can be compared. The aim of this study was to assemble high-quality haplotype phased genomes for Eucalyptus urophylla and E. grandis. Using Nanopore sequencing data generated for an E. urophylla x E. grandis F1 hybrid and a trio-binning approach, we successfully assembled 544.51 Mb of the E. urophylla haplogenome (contig N50 of 1.93 Mb) and 566.75 Mb of the E. grandis haplogenome (contig N50 of 2.42 Mb) with a BUSCO completion score of 98.8%. Using high-density SNP genetic linkage maps of both parents, more than 88% of the haplogenome contigs could be anchored to one of the eleven chromosomes (scaffold N50 of 42.45 Mb and 43.82 Mb for the E. urophylla and E. grandis haplogenome assemblies, respectively). We also provide the first genome-wide comparison between the E. urophylla and E. grandis using the Synteny and Rearrangement Identifier (SyRI) to identify SVs, leading to the discovery of 48,729 SVs between the two haplogenomes. This study is the first step towards implementing haplotype-informed molecular breeding of Eucalyptus tree species.en_ZA
dc.description.availabilityUnrestricteden_ZA
dc.description.degreeMSc (Genetics)en_ZA
dc.description.departmentGeneticsen_ZA
dc.description.sponsorshipThe National Research Foundation of South Africa, the South African Department of Science and Innovation, the Technology Innovation Agency and Technology and Human Resources for Industry Programmeen_ZA
dc.identifier.citationLötter et al., 2021, Haplotype-resolved genome assembly of an F1 hybrid of Eucalyptus urophylla x E. grandis, MSc thesis, University of Pretoria, Pretoria http://hdl.handle.net/2263/83845en_ZA
dc.identifier.otherA2022en_ZA
dc.identifier.urihttp://hdl.handle.net/2263/83845
dc.language.isoenen_ZA
dc.publisherUniversity of Pretoria
dc.rights© 2022 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.subjectGeneticsen_ZA
dc.subjectUCTD
dc.titleHaplotype-resolved genome assembly of an F1 hybrid of Eucalyptus urophylla x E. grandisen_ZA
dc.typeDissertationen_ZA

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