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Assistant Professor of Biological Sciences
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![]() Brassican napus allopolyploids (middle) are resynthesized by crossing rapid cycling, self-compatible doubled haploid lines of B. oleracea (left) and B.rapa (right) followed by colchicine treatment. The allopolyploids have novel phenotypes (e.g., hybrid vigor) in comparison to their diploid progenitors. The diploids are actually ancient polyploids, making Brassica a model system for studying layers of genome duplication. Research description Research in our lab broadly encompasses plant evolutionary biology—from phylogenetic studies in plant diversity to genome-wide analyses of gene expression. Current investigations are directed at molecular systematics and comparative genomics (phylogenomics), with a particular focus on the evolution and ecology of polyploid plants. Polyploidy, the process of genome doubling that gives rise to organisms with multiple sets of chromosomes is a major evolutionary force in both plants and animals. More than 70% of flowering plants have had at least one polyploid event in their lineage. Many important crop plants—such as alfalfa, cotton, potato, and wheat—are obvious polyploids while others—such as maize, soybean, and cabbage—retain the vestiges of ancient polyploid events. My leading conceptual questions pertain to the consequences of genome doubling, such as deciphering the mechanisms that give rise to novel morphological or ecological features found in polyploids. Understanding the pattern of how such novelty might arise requires an understanding of the evolutionary history of polyploid plants and their diploid relatives. We have two ongoing research projects that synthesize evolutionary and genomic approaches: Selected publicationsPires, J.C., and K.L. Hertweck. 2008. A renaissance of cytogenetics: studies in polyploidy and chromosomal evolution. Annals of Missouri Botanical Garden 95: 275-281. Gaeta, R.T., Pires, J.C., Iniguez-Luy, F., Leon, E., and T.C. Osborn. 2007. Genomic changes in resynthesized Brassica napus: The effect of genomic changes on gene expression and phenotypic variation. The Plant Cell 19: 3403-3417. Telgmann, A., Jasmari, A., Kinney, M.S., Pires, J.C., and C. Jung. 2007. Genetic and physical maps around the sex gene of the dioecious plant asparagus (Asparagus officinalis). Molecular Genetics and Genomics 278: 221-234. Pires J.C., I.J. Maureira, T.J. Givish, K.J. Sytsma, G. Petersen, O. Seberg, C. Asmussen, J.I. Davis, D.W. Stevenson, P.J. Rudall, M.F. Fay,and M.W. Chase. 2006. Phylogeny, genome size, and chromosome evolution of the Asparagales. Aliso 22: 287-304 Bogler, D.J., Pires, J.C. and Francisco-Ortega, J. 2006. Phylogeny of Agavaceae based on ndhF, rbcL, and ITS rDNA: Implications of molecular data for classification. Aliso 22: 313-328. Lukens, L.N., Pires, J.C., Leon, E., Vogelzang, R.D., Oslach, L. and Osborn, T.C. 2006. Patterns of sequence loss and cytosine methylation within a population of newly resynthesized Brassica napus. Plant Physiology, Vol. 140: 336-348. dePamphilis, C., deSalle, R., Doyle, J.J., Eisen, J.A., Gu, X., Harshman, J., Jansen, R.K., Kellogg, E.A., Koonin, E.V., Mishler, B.D., Philippe, H., Pires, J.C., Qiu, Y.L., Rhee, S.Y., Sjolander, K., Soltis, D.E., Soltis, P.S., Stevenson, D.W., Wall, K., Warnow, T., and C. Zmasek. 2006. Taking the first steps towards a standard for reporting on phylogenies: minimal information about a phylogenomic analysis (MIAPA). OMICS A Journal of Integrative Biology 10: 231-237. |
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| Biological Sciences | 105 Tucker Hall | Columbia, MO 65211-7400 | phone: 573-882-6659 | email: blairjo@missouri.edu © 2000 Curators of the University of Missouri | equal opportunity/ADA institution | last modified: 23-Nov-2009 | ||