Rozprawy doktorskie na temat „Plant genome mapping”
Utwórz poprawne odniesienie w stylach APA, MLA, Chicago, Harvard i wielu innych
Sprawdź 50 najlepszych rozpraw doktorskich naukowych na temat „Plant genome mapping”.
Przycisk „Dodaj do bibliografii” jest dostępny obok każdej pracy w bibliografii. Użyj go – a my automatycznie utworzymy odniesienie bibliograficzne do wybranej pracy w stylu cytowania, którego potrzebujesz: APA, MLA, Harvard, Chicago, Vancouver itp.
Możesz również pobrać pełny tekst publikacji naukowej w formacie „.pdf” i przeczytać adnotację do pracy online, jeśli odpowiednie parametry są dostępne w metadanych.
Przeglądaj rozprawy doktorskie z różnych dziedzin i twórz odpowiednie bibliografie.
Fisk, Dianna G. "CRP1 : founding member of a novel protein family that functions in organellar gene expression /". view abstract of download file of text, 2000. http://wwwlib.umi.com/cr/uoregon/fullcit?p9987422.
Pełny tekst źródłaIslam, Mohammad Sayedul. "Genetic mapping of rooting in rice : exploiting a high throughput phenotyping in plants". Thesis, University of Aberdeen, 2016. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=229720.
Pełny tekst źródłaSmith, Gavin James. "A molecular systematic study of the xylariales (ascomycota)". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2003. http://hub.hku.hk/bib/B30110841.
Pełny tekst źródłaSong, Weining. "Genome studies of cereals /". Title page, contents and summary only, 1992. http://web4.library.adelaide.edu.au/theses/09PH/09phs6984.pdf.
Pełny tekst źródłaLonergan, Paul Francis. "Genetic characterisation and QTL mapping of zinc nutrition in barley (Hordeum vulgare)". Title page, contents and abstract only, 2001. http://web4.library.adelaide.edu.au/theses/09PH/09phl847.pdf.
Pełny tekst źródłaDimkpa, Stanley Obumneke Nyebuhi. "Genome wide association mapping and assessment of allelic variation in strigolactone synthesis genes involved in rice plant parasite interactions". Thesis, University of Aberdeen, 2014. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=220456.
Pełny tekst źródłaDonald, Tamzin. "Organisation and expression of plant B chromosomes /". Title page, table of contents and abstract only, 1999. http://web4.library.adelaide.edu.au/theses/09PH/09phd6758.pdf.
Pełny tekst źródłaHanson, Christopher Jon. "Exploration of the Gossypium raimondii Genome Using Bionano Genomics Physical Mapping Technology". BYU ScholarsArchive, 2018. https://scholarsarchive.byu.edu/etd/6854.
Pełny tekst źródłaJean, Martine. "Genetic mapping of restorer genes for cytoplasmic male sterility in Brassica napus using DNA markers". Thesis, McGill University, 1995. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=40147.
Pełny tekst źródłaSurber, Lisa Marie McKinley. "Is there a genetic basis for forage quality of barley for beef cattle?" Diss., Montana State University, 2006. http://etd.lib.montana.edu/etd/2006/surber/SurberL0806.pdf.
Pełny tekst źródłaXing, Liqun 1962. "Marker density, marker distribution and QTL-by-environment interaction in QTL mapping". Thesis, McGill University, 1999. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=36734.
Pełny tekst źródłaSchneerman, Martha June Cook Weber David F. "Identification of quantitative trait loci (QTLs) of corn oil in Zea mays L". Normal, Ill. Illinois State University, 1996. http://wwwlib.umi.com/cr/ilstu/fullcit?p9720812.
Pełny tekst źródłaTitle from title page screen, viewed May 31, 2006. Dissertation Committee: David F. Weber (chair), Alan J. Katz, Marjorie A. Jones, Radheshyam K. Jayaswal, Jefferey A. Dole. Includes bibliographical references (leaves 96-108) and abstract. Also available in print.
Campeol, Nadia. "Detection of markers in a low-density region of the barley (Hordeum vulgare L.) genome and their effects on the mapping of quantitative traits". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape10/PQDD_0002/MQ44137.pdf.
Pełny tekst źródłaPollock, Stephanie. "A study of genetic diversity and genome organization of Brassica napus using EST (expressed sequence tags) of Arabidopsis and SSR (simple sequence repeat) markers of B. napus /". Thesis, McGill University, 2001. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=33023.
Pełny tekst źródłaHraber, Peter T. "Discovering molecular mechanisms of mututalism with computational approaches to endosymbiosis /". Color figures, full content, and supplementary materials are available online, 2001.
Znajdź pełny tekst źródła"July, 2001." Includes bibliographical references (leaves 112-121). Color figures, full content, and supplementary materials are available online via www.santafe.edu/p̃th/dss.
Wargachuk, Richard Burns. "Fine mapping and functional analysis of the radish Rfo nuclear restorer locus". Thesis, McGill University, 2004. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=81454.
Pełny tekst źródłaSadeghzadeh, Behzad. "Mapping of chromosome regions associated with seed zinc accumulation in barley". University of Western Australia. School of Earth and Geographical Sciences, 2008. http://theses.library.uwa.edu.au/adt-WU2008.0204.
Pełny tekst źródłaVeereshlingam, Harita. "Characterization of Infection Arrest Mutants of Medicago Truncatula and Genetic Mapping of Their Respective Genes". Thesis, University of North Texas, 2005. https://digital.library.unt.edu/ark:/67531/metadc5567/.
Pełny tekst źródłaWilson, Dale 1972. "Early-flowering mutants of a late-flowering ecotype of Arabidopsis thaliana". Monash University, Dept. of Biological Sciences, 2001. http://arrow.monash.edu.au/hdl/1959.1/8976.
Pełny tekst źródłaGeddy, Rachel Gwyneth. "Location and expression of genes related to the cytoplasmic male sterility system of Brassica napus". Thesis, McGill University, 2006. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=100608.
Pełny tekst źródłaRestoration of fertility in Brassica napus nap and pol CMS is associated with nuclearly encoded genes Rfn and Rfp, respectively. These restorers are very closely linked to one another, and may be allelic. Further efforts to isolate Rfp have narrowed the genomic region to approximately 105 kb of a syntenic region in Arabidopsis thaliana. Cosmid clones isolated from a library of Brassica rapa genomic DNA introgressed with Rfp have been successfully sorted into contigs through the application of the amplified fragment length polymorphism technique. The region to which Rfp is mapped is syntenic to a region of Arabidopsis DNA that is a duplication of a second location at the 23 megabase region of chromosome 1 of that genome. This region contains pentatricopeptide (PPR) motif-encoding genes that are highly related to other restorers of fertility of other species. By inference, Rfp from Brassica napus may encode PPR motifs. The PPR genes related to these previously characterized restorers of fertility are often found alongside the restorer genes existing as mini-clusters of several PPR-encoding genes. This is likely caused by selective pressure acting on PPR-encoding genes that resulted in diversification and multiplication of these genes. In addition, the PPR genes of this duplicated region are not syntenically located, whereas the non-PPR-encoding genes maintain their syntenic locations. The same is true for orthologous comparisons between Arabidopsis and other plant species. PPR genes are therefore malleable and capable of alteration in response to changing environmental pressures, such as the evolution of sterility inducing genes.
Boyko, Oleksandr, i University of Lethbridge Faculty of Arts and Science. "The versatile role of homologous recombination in plant cell : repair of DNA damage, stress-directed genome evolution and foreign DNA integration". Thesis, Lethbridge, Alta. : University of Lethbridge, Faculty of Arts and Science, 2008, 2008. http://hdl.handle.net/10133/724.
Pełny tekst źródłaxxi, 246 leaves : ill. ; 29 cm. --
Nualsri, Charassri. "Inheritance of rhizome expression in birdsfoot trefoil (Lotus corniculatus l.) /". free to MU campus, to others for purchase, 1996. http://wwwlib.umi.com/cr/mo/fullcit?p9717176.
Pełny tekst źródłaHayes, Alec J. "Characterization of the soybean genome in regions surrounding two loci for resistance to soybean mosaic virus". Diss., Virginia Tech, 1998. http://hdl.handle.net/10919/11275.
Pełny tekst źródłaPh. D.
Karps, Jennifer Michelle. "Regeneration Patterns and Facilitation Following Blowdown in a Self- Replacing Lodgepole Pine (Pinus contorta) Stand in Central Oregon". PDXScholar, 2006. https://pdxscholar.library.pdx.edu/open_access_etds/1482.
Pełny tekst źródłaMorris, Viktoriya. "Map-based cloning of the NIP gene in model legume Medicago truncatula". Thesis, University of North Texas, 2007. https://digital.library.unt.edu/ark:/67531/metadc3638/.
Pełny tekst źródłaSharp, Aaron Robert. "Improving Cotton Agronomics with Diverse Genomic Technologies". BYU ScholarsArchive, 2016. https://scholarsarchive.byu.edu/etd/5845.
Pełny tekst źródłaHerzig, Paul [Verfasser], Klaus [Gutachter] Pillen i Jens [Gutachter] Léon. "Genome-wide association studies in a wild barley nested association mapping (NAM) population to reveal the genetic architecture of plant development and quality traits / Paul Herzig ; Gutachter: Klaus Pillen, Jens Léon". Halle (Saale) : Universitäts- und Landesbibliothek Sachsen-Anhalt, 2021. http://d-nb.info/1238074561/34.
Pełny tekst źródłaHowie, John Allan. "Adult plant resistance to fungal pathogens of wheat". Thesis, Open University, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.388302.
Pełny tekst źródłaBassi, Filippo Maria. "Radiation Hybrid Fine Mapping of Two Fertility-Related Genes: Marking the Path to Wheat Hybrids". Diss., North Dakota State University, 2012. https://hdl.handle.net/10365/26535.
Pełny tekst źródłaKuraparthy, Vasu. "Genomic targeting and mapping of agronomically important genes in wheat". Diss., Manhattan, Kan. : Kansas State University, 2007. http://hdl.handle.net/2097/311.
Pełny tekst źródłaBickel, Cory Lyn. "Identification of Genomic Regions Involved in Stress Responsiveness in Flax by Genetic Mapping". Case Western Reserve University School of Graduate Studies / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=case1301676557.
Pełny tekst źródłaBalimponya, Elias George. "Application of Genomic Selection and Association Mapping to Breeding for Resistance to Rice Blast and Bacterial Blight of Rice (Oryza sativa L.)". The Ohio State University, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=osu1449138999.
Pełny tekst źródłaGagliardi, Paulo Roberto. "Análise estrutural e comparativa do genoma de Leifsonia xyli subsp. xyli". Universidade de São Paulo, 2003. http://www.teses.usp.br/teses/disponiveis/11/11135/tde-20102003-165028/.
Pełny tekst źródłaLeifsonia xyli subsp. xyli (Davis et al.; 1984; Evtushenko et al.; 2000) is the causal agent of one of the most economically important disease of sugarcane worldwide, i.e, ratoon stunting disease (Gillaspie Jr. & Davis, 1992; Davis et al.; 1994). The main objective of this study was to confirm the assembly of the genome of L. xyli subsp. xyli obtained after shotgun sequencing by the Agronomic and Enviromental Genomes group of the ONSA/FAPESP network. The identity of the strain was confirmed by amplification and sequencing of the 23S rRNA region as well as by microaglutination serological tests with specific antiserum. Besides this, scanning electron microscopic analysis was used to assess the purity of the strain culture. The size of the genome of L. xyli subsp. xyli was estimated based on restriction analysis after digestion of genomic DNA with SpeI and XbaI followed by pulsed-field gel electrophoresis. The estimates of 2,530 kb and 2,540 kb, respectively for SpeI and XbaI, are in agreement with the one obtained by whole genome sequencing (2,596 kb). In addition, the number of repeated sequences and ribossomal genes predicted by thesequencing project was confirmed by hybridization experiments with the appropriate probes. Genomic comparisons of L. xyli subsp. xyli, L. xyli subsp. cynodontis and two Clavibacter species comprised a second objective of this study. Comparisons were based on RFLP analysis after hybridization of digested genomic DNA using mobile genetic elements present in the genome of L. xyli subsp. xyli as probes. The estimates of number of copies of these elements in the genome of L. xyli subsp. xyli obtained by this approach agreed with the ones obtained by sequencing if RFLP fragments smaller than 9 kb are considered. Data from larger fragments were not obtained since they were not adequately resolved by electrophoresis. Finally, RFLP and rep-PCR comparisons unveiled differences between L. xyli subsp. xyli and L. xyli subsp. cynodontis as well as between these and Clavibacter. No differences were found between strain CTC B07 of L. xyli subsp. xyli and an Australian strain.
Laurent, Benoit. "Base génétique et potentiel d’évolution de la pathogénicité de Fusarium graminearum, bio-agresseur fongique des céréales". Thesis, Bordeaux, 2016. http://www.theses.fr/2016BORD0317/document.
Pełny tekst źródłaF. graminearum is one of the main causal agents of the fusarium head-blight (FHB), a cereal disease leading to head necrosis, in addition to grain and food/feed contamination by stable and toxic metabolites. Recent observations refer to an increase of pathogenicity, questioning efficiency and durability of current management practices. In order to anticipate this evolution, we must bring a deeper characterization of the currently existing diversity. Six new genomes of F. graminearum were sequenced, and 243,000 genetic variations have been identified and characterized. Seventy seven percent of the total number of the variants was located within 32% of the genome, delineating highly polymorphic islands. These islands are enriched with probable effectors linked to Fusarium’s pathogenicity. The construction and the genotyping on 1,300 molecular markers of a recombinant population have enabled the development of the first high-density genetic map of the species. The remarkable correlation between polymorphism and recombination rate highlighted the 'two-speed' genome organization of this pathogen. Finally, the integration of these data through a quantitative genetic approach allowed the discovery of one quantitative trait locus, likely to affect the gene FgVeA, and responsible for 90% of the observed variation of aggressiveness and mycotoxin production. These results are discussed in the light of F. graminearum’s adaptive potential and evolution
Gilmore, Scott R. "Genetic mapping of plant transpiration efficiency". Phd thesis, 2005. http://hdl.handle.net/1885/149993.
Pełny tekst źródłaJaccoud, Damian Francois. "Diversity arrays technology (DArT) in a model plant and animal". Phd thesis, 2006. http://hdl.handle.net/1885/150431.
Pełny tekst źródłaDonald, Tamzin. "Organisation and expression of plant B chromosomes / by Tamzin Donald". Thesis, 1999. http://hdl.handle.net/2440/19416.
Pełny tekst źródłaBibliography: leaves 217-233.
xix, 233 leaves : ill. (some col.) ; 30 cm.
The rDNA work presented aimed to determine if B chromosome sequences of Brachycome dichromosomatica were transcriptionally active.
Thesis (Ph.D.)--University of Adelaide, Dept. of Genetics, 1999
Oziel, Adeline M. "Mapping of quantitative trait loci for malting quality in a winter X spring barley (Hordeum vulgare, L.) cross". Thesis, 1993. http://hdl.handle.net/1957/35753.
Pełny tekst źródłaGraduation date: 1994
"Genome sequence of shiitake mushroom Lentinula edodes and comparative mushroom genomics with platform construction". Thesis, 2011. http://library.cuhk.edu.hk/record=b6075378.
Pełny tekst źródłaThesis (Ph.D.)--Chinese University of Hong Kong, 2011.
Includes bibliographical references (leaves 124-146).
Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web.
Abstract also in Chinese.
"Generation and sequencing of cDNA matching SAGE tags for gene identification in Lentinula edodes". 2005. http://library.cuhk.edu.hk/record=b5896450.
Pełny tekst źródłaThesis (M.Phil.)--Chinese University of Hong Kong, 2005.
Includes bibliographical references (leaves 166-172).
Abstracts in English and Chinese.
Abstract --- p.iii
Acknowledgments --- p.vi
Abbreviations --- p.vii
Table of Contents --- p.viii
Table of Figures --- p.xiii
Table of Tables --- p.xviii
Chapter Chapter 1. --- Literature Reviews
Chapter 1.1 --- Functional Genomics and Its Developments --- p.1
Chapter 1.1.1 --- Introduction --- p.1
Chapter 1.1.2 --- "Transcriptomics, Proteomics and Metabolomics" --- p.1
Chapter 1.1.3 --- Gene-perturbing Strategies --- p.3
Chapter 1.1.4 --- Applications of Functional Genomics --- p.4
Chapter 1.2 --- Serial Analysis of Gene Expression (SAGE) and Generation of Longer cDNA Fragments from SAGE tags for Gene Identification (GLGI) --- p.6
Chapter 1.2.1 --- Introduction --- p.6
Chapter 1.2.2 --- Principles and Methods of SAGE --- p.6
Chapter 1.2.3 --- Data Analysis --- Bioinformatics --- p.9
Chapter 1.2.4 --- Applications of SAGE --- p.9
Chapter 1.2.5 --- Modifications of SAGE --- p.10
Chapter 1.2.6 --- Principles and Methods of GLGI --- p.11
Chapter 1.2.7 --- Applications and Improvements of GLGI --- p.14
Chapter 1.3 --- Transformation --- p.15
Chapter 1.3.1 --- Introduction --- p.15
Chapter 1.3.2 --- Different Methods of Transformation --- p.15
Chapter 1.3.2.1 --- General Transformation Strategy --- p.15
Chapter 1.3.2.2 --- Polyethylene Glycol (PEG)-mediated Transformation --- p.16
Chapter 1.3.2.3 --- Restriction Enzyme Mediated Integration (REMI) --- p.16
Chapter 1.3.2.4 --- Electroporation --- p.17
Chapter 1.3.2.5 --- Particle Bombardment --- p.17
Chapter 1.3.3 --- The Future Needs of Transformation --- p.18
Chapter 1.4 --- RNA Silencing --- p.20
Chapter 1.4.1 --- Introduction --- p.20
Chapter 1.4.2 --- Major Components and Principles of RNAi --- p.21
Chapter 1.4.3 --- Applications of RNA Silencing --- p.23
Chapter 1.5 --- The Target Organism Lentinula edodes --- p.25
Chapter 1.5.1 --- Introduction --- p.25
Chapter 1.5.2 --- The Life Cycle of L. edodes --- p.26
Chapter 1.5.3 --- Biochemical and Molecular Studies on L. edodes --- p.27
Chapter 1.5.4 --- Prospectus --- p.29
Chapter Chapter 2. --- Development of Methods for Studying Gene Function in Lentinula edodes
Chapter 2.1 --- Introduction --- p.30
Chapter 2.2 --- Materials and Methods --- p.32
Chapter 2.2.1 --- Cultivation of Lentinula edodes --- p.32
Chapter 2.2.2 --- Proplast Release and Regeneration --- p.32
Chapter 2.2.3 --- Preparation of Plasmid DNA --- p.33
Chapter 2.2.4 --- Selectable Marker …Bialaphos --- p.35
Chapter 2.2.5 --- Transformation --- p.35
Chapter 2.2.5.1 --- Electroporation --- p.35
Chapter 2.2.5.2 --- PEG-mediated Transformation --- p.36
Chapter 2.3 --- Results --- p.37
Chapter 2.3.1 --- Cultivation of Lentinula edodes --- p.37
Chapter 2.3.2 --- Proplast Release and Regeneration --- p.37
Chapter 2.3.3 --- Preparation of Plasmid DNA --- p.43
Chapter 2.3.4 --- Selectable Marker--- Bialaphos --- p.43
Chapter 2.3.5 --- Transformation --- p.46
Chapter 2.3.5.1 --- Electroporation --- p.46
Chapter 2.3.5.2 --- PEG-mediated Transformation --- p.46
Chapter 2.4 --- Discussions and Conclusions --- p.57
Chapter Chapter 3. --- Identification of Interested Genes in Expression Profile of SAGE using GLGI Method.
Chapter 3.1 --- Introduction --- p.61
Chapter 3.1.1 --- Results of SAGE Analysis --- p.61
Chapter 3.1.2 --- Use of GLGI Method for Extension of SAGE Tags --- p.63
Chapter 3.1.3 --- 5´ة Extension of GLGI (5'GLGI) --- p.65
Chapter 3.1.3.1 --- Introduction --- p.65
Chapter 3.1.3.2 --- "Overall strategy of 5, GLGI Method" --- p.67
Chapter 3.1.3.3 --- Two-Steps PCR Method --- p.69
Chapter 3.2 --- Generation of Longer cDNA Fragments from SAGE tags for Gene Identification (GLGI) --- p.71
Chapter 3.2.1 --- Materials and Methods (GLGI Analysis) --- p.71
Chapter 3.2.1.1 --- Total RNA Extraction --- p.71
Chapter 3.2.1.2 --- Messenger RNA (mRNA) Extraction --- p.72
Chapter 3.2.1.3 --- Preparation of 3´ة cDNA for GLGI --- p.73
Chapter 3.2.1.4 --- NIaIII digestion of double strand cDNA --- p.74
Chapter 3.2.1.5 --- PCR amplification of the 3'-cDNAs (Optional) --- p.77
Chapter 3.2.1.6 --- GLGI Amplification of The Target Template --- p.80
Chapter 3.2.1.7 --- DNA Cloning (Optional) --- p.82
Chapter 3.2.1.8 --- Sequencing of GLGI PCR products --- p.85
Chapter 3.2.2 --- 5' Materials and Methods (5' GLGI Analysis) --- p.86
Chapter 3.2.2.1 --- Preparation of unique antisense primers --- p.86
Chapter 3.2.2.2 --- 5' extension of GLGI products --- p.87
Chapter 3.2.2.3 --- DNA Cloning (Optional) --- p.89
Chapter 3.2.2.4 --- Sequencing of 5' GLGI PCR products --- p.89
Chapter 3.2.3 --- Results (GLGI Analysis) --- p.90
Chapter 3.2.3.1 --- Total RNA Extraction --- p.90
Chapter 3.2.3.2 --- Messenger RNA Extraction --- p.90
Chapter 3.2.3.3 --- Preparation of 3' cDNA for GLGI --- p.90
Chapter 3.2.3.4 --- NIaIII digestion of double strand cDNA --- p.94
Chapter 3.2.3.5 --- GLGI Amplification of The Target Template --- p.94
Chapter 3.2.3.6 --- Sequencing of GLGI PCR products --- p.103
Chapter 3.2.4 --- Results (5' GLGI Analysis) --- p.111
Chapter 3.2.4.1 --- 5' extension of GLGI products --- p.111
Chapter 3.2.4.2 --- Sequencing of 5´ة GLGI PCR products --- p.116
Chapter 3.3 --- Discussions and Conclusions --- p.126
Chapter 3.3.1 --- GLGI amplification of the target template --- p.126
Chapter 3.3.2 --- 5' extension of GLGI products --- p.129
Chapter 3.3.3 --- Two-Steps PCR Method --- p.130
Chapter 3.3.4 --- Sequencing results of GLGI method and 5' GLGI method --- p.131
Chapter Chapter 4. --- Identification of Unknown EST Using PCR Method With cDNA Library
Chapter 4.1 --- Introduction --- p.134
Chapter 4.2 --- Materials and Methods --- p.134
Chapter 4.2.1 --- Extension of 5' end of EST sequence by PCR method --- p.134
Chapter 4.2.2 --- Purification of PCR products --- p.136
Chapter 4.2.3 --- Sequencing of Extended EST products --- p.136
Chapter 4.3 --- Results --- p.137
Chapter 4.3.1 --- Extension of 5' end of EST sequence by PCR method --- p.137
Chapter 4.3.2 --- Sequencing of Extended EST products --- p.137
Chapter 4.4 --- Discussions and Conclusions --- p.147
Chapter Chapter 5. --- General Discussions --- p.151
Appendix I --- p.156
Reference --- p.166
Zurek, Paul Roman. "Quantitative Trait Locus Mapping Reveals Regions of the Maize Genome Controlling Root System Architecture". Diss., 2014. http://hdl.handle.net/10161/9399.
Pełny tekst źródłaRoot system architecture (RSA) is the spatial distribution of roots of individual plants. As part of a collaborative effort I adapted a gellan gum based system for imaging and phenotyping of root systems in maize. This system was first used to perform a survey of 26 distinct maize varieties of the Nested Association Mapping (NAM) population. The analysis of these data showed a large amount of variation between different RSA, in particular demonstrating tradeoffs between architectures favoring sparse, but far reaching, root networks versus those favoring small but dense root networks. To study this further I imaged and phenotyped the B73 (compact) x Ki3 (exploratory) mapping population. These data were used to map 102 quantitative trait loci (QTL). A large portion of these QTL had large, ranging from 5.48% to 23.8%. Majority of these QTLs were grouped into 9 clusters across the genome, with each cluster favoring either the compact of exploratory RSA. In summary, our study demonstrates the power of the gellan based system to locate loci controlling root system architecture of maize, by combining rapid and highly detailed imaging techniques with semi-automated computation phenotyping.
Dissertation
Mumm, Anina. "Promoter analysis of members of a plant defense-related LRR-RLK gene cluster in Arabidopsis thaliana". Thesis, 2014. http://hdl.handle.net/10210/11414.
Pełny tekst źródłaA 14-member, closely-spaced cluster of genes coding for leucine-rich repeat receptor-like kinases (LRR-RLKs) is located on chromosome 1 of Arabidopsis thaliana. Following on from previous microarray studies that found some of the members of this cluster to be upregulated in response to biotic stressors, including the bacterial elicitor flg22, the present study sought to confirm, using a luciferase-based protoplast assay, that flg22 does in fact induce the expression of the genes, and then to investigate the promoters of the genes. The promoters of At1g51790, At1g51850 and At1g51890 responded positively in this particular assay, and bioinformatic analyses determined that W-boxes are over-represented in the cloned regions. Mutational inactivation of individual W-boxes in the promoter of At1g51790 drastically reduced the flg22 response, except for the W-box closest to the start site, which seemed to increase both basal and flg22-inducible expression. In the promoter of At1g51850, mutational inactivation of either or both of its W-box dyads resulted in virtually no flg22 inducibility. The deletion of 6 W-boxes in the promoter of At1g51890, done via truncation, drastically reduced both its basal expression and its inducible response to flg22. These results provide evidence that W-box cis-elements are responsible for the upregulation of these LRR-RLKs in response to flg22. WRKYs -7, -11, -22,and -26 were found bioinformatically to have similar expression patterns to some of the genes in the cluster, and are thus good candidates to investigate as transcriptional regulators of the cluster in future studies.
Song, Weining 1958. "Genome studies of cereals". 1992. http://web4.library.adelaide.edu.au/theses/09PH/09phs6984.pdf.
Pełny tekst źródłaLonergan, Paul F. "Genetic characterisation and QTL mapping of zinc nutrition in barley (Hordeum vulgare) / Paul Francis Lonergan". 2001. http://hdl.handle.net/2440/21718.
Pełny tekst źródłax, 211 leaves : ill. ; 30 cm.
Title page, contents and abstract only. The complete thesis in print form is available from the University Library.
Maps major genes or quantitative trait loci associated with zinc nutrition in the vegetative and reproductive tissues of barley (Hordeum vulgare)
Thesis (Ph.D.)--University of Adelaide, Dept. of Plant Science, 2001
Lee, Young-Kwang. "Molecular and functional studies of low molecular weight glutenin subunits from A-genome diploid wheats". Phd thesis, 1997. http://hdl.handle.net/1885/145939.
Pełny tekst źródłaSong, Weining 1958. "Genome studies of cereals / by Song Weining". Thesis, 1992. http://hdl.handle.net/2440/21422.
Pełny tekst źródła114, [43] leaves, [30] leaves of plates : ill. ; 30 cm.
This thesis investigates genome analysis of wheat, rye and barley. The objective is to evaluate the feasibility of using polymerase chain reaction (PCR) as a tool for studying cereal genomes. Results are compared for PCR and RFLP (restriction fragment length polymorphism)
Thesis (Ph.D.)--University of Adelaide, Dept. of Plant Science, 1994
Araneda, Loreto P. "Comparative Genome Analysis between Agrostis stolonifera and Members of the Pooideae Subfamily Including Brachypodium distachyon". 2011. https://scholarworks.umass.edu/theses/661.
Pełny tekst źródłaMing, Reiguang. "Restriction fragment length polymorphism analysis of host-plant resistance to four maize pathogens". Thesis, 1995. http://hdl.handle.net/10125/9273.
Pełny tekst źródłaLong, Nigel R. "Characterisation and mapping of chromosome regions associated with improved growth and grain yield of barley on sandy soils of low fertility / by Nigel Richard Long". 2003. http://hdl.handle.net/2440/21993.
Pełny tekst źródłaIncludes bibliographical references (leaves 260-292)
v, 294 leaves : ill. (some col.), plates (col.), maps (col.) ; 30 cm.
Title page, contents and abstract only. The complete thesis in print form is available from the University Library.
Thesis (Ph.D.)--University of Adelaide, School of Agriculture and Wine, 2003
Long, Nigel R. "Characterisation and mapping of chromosome regions associated with improved growth and grain yield of barley on sandy soils of low fertility / by Nigel Richard Long". Thesis, 2003. http://hdl.handle.net/2440/21993.
Pełny tekst źródłaIncludes bibliographical references (leaves 260-292)
v, 294 leaves : ill. (some col.), plates (col.), maps (col.) ; 30 cm.
Thesis (Ph.D.)--University of Adelaide, School of Agriculture and Wine, 2003