Browsing by Subject "apomixis"
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Item An analysis of alternative forms of plant reproduction using Gossypium barbadense and Arabidopsis thaliana(2009-05-15) Biddle, Kelly DeniseApomixis holds vast potential for improving agriculture worldwide. It would make plant breeding faster, allow for fixation of hybrid genotypes, and help genetically isolate transgenic crops. However, efforts to introduce apomixis into agriculturally important crops, through either plant breeding or molecular genetics, have failed to produce any new apomictic varieties. This could possibly be remedied if researchers better understood the genetics of apomixis, including the underlying genes, their regulation, and the cellular pathways they control. My work increased our knowledge of these processes by using a mixture of novel methods and underutilized resources. In this study I pursued a two-pronged approach that involved both traditional and reverse molecular genetic techniques. I analyzed the Semigamy mutation from Pima Cotton (Gossypium barbadense), which produces large numbers of haploid and chimeric offspring. Although interesting and potentially useful, little is known about this gene, its expression, regulation, and localization, or the cellular processes in which it is involved. This knowledge advanced our understanding of both this part of apomixis and plant reproduction in general. I was able to determine that the Semigamy mutation is recessive to the wild-type and is incompletely expressed even in the homozygous state. Second, I attempted to recreate the various steps of apomixis in the model species Arabidopsis thaliana using the host of tools made available by its fully sequenced genome. Mutants in various organisms, including microbes, plants, and animals, have phenotypes resembling various components of apomixis, and the sequences of most of the genes involved are available in public databases. I identified homologous Arabidopsis genes by comparing these sequences against the entire Arabidopsis genome. Mutants carrying altered versions of these genes were then studied and characterized using various techniques to see if they had any effect on plant reproduction. This method had not been used to study apomixis before this study and revealed several new reproductive Arabidopsis mutations, specifically those in genes homologous to the S. cerevisiae ste12 and rec8 genes. These results will advance the study of apomixis and potentially enable researchers to one day apply it to agriculturally important crop species.Item Molecular tools for marker-assisted breeding of buffelgrass(Texas A&M University, 2005-11-01) Jessup, Russell WilliamThe increasing availability of molecular tools is facilitating marker-assisted selection (MAS) in plant improvement programs. The objectives of this research were to: 1) populate the framework buffelgrass genome map with additional molecular markers, 2) develop polymerase chain reaction (PCR)-based markers from selected, informative restriction fragment length polymorphism (RFLP) markers on the buffelgrass genome map, and 3) increase marker resolution near the locus conferring apomixis (PApo1). Buffelgrass [Pennisetum ciliare (L.) Link syn. Cenchrus ciliaris L.] (2n=4x=36), a highly polymorphic, apomictic, perennial forage grass, is well-suited for genetic linkage analyses. One hundred and seventy one probes from an apomictic, spikelet-specific, complementary deoxyribonucleic acid (cDNA) library and 70 expressed sequence tag simple sequence repeats (EST-SSRs) from apomictic pistil cDNAs were evaluated and added to the framework buffelgrass genome map. The improved linkage map contains 851 markers from 11 grass species and covers approximately 80-85% of the buffelgrass genome. Two RFLPs from the buffelgrass genome map were converted to PCR-based markers for both the identification of hybrids and quantification of sexual versus apomictic reproduction. A gel-free, high-throughput technique was developed to analyze these markers directly in 96-well plates. Five additional markers were placed onto the buffelgrass linkage group with the PApo1 apomixis locus through comparative mapping of candidate orthologs from the sorghum genome map and bulked-segregant analysis of amplified-fragment-lengthpolymorphisms (BSA-AFLP). Increasing the mapping population size did not increase map resolution in the PApo1 region. Association mapping revealed that the recombination suppression near PApo1 is moderate and would complicate comparative map-based cloning efforts of the orthologous region in sorghum.