David W Galbraith

David W Galbraith

Professor, Plant Science
Professor, Biomedical Engineering
Professor, BIO5 Institute
Primary Department
Department Affiliations
Contact
(520) 621-9153

Work Summary

I examine the molecular functions of the different cells found in the tissues and organs of plants and animals and how they combine these functions to optimize the health and vigor of the organism.

Research Interest

David Galbraith obtained undergraduate and graduate degrees in Biochemistry from the University of Cambridge, and postdoctoral training as a NATO Fellow at Stanford University. His first academic appointment was at the University of Nebraska Lincoln, and he became Professor of Plant Sciences at the University of Arizona in 1989. His research has focused on the development of instrumentation and methods for the analysis of biological cells, organs, and systems. He is internationally recognized as a pioneer in the development and use of flow cytometry and sorting in plants, developing widely-used methods for the analysis of genome size and cell cycle status, and for the production of somatic hybrids. He also was among the first to develop methods for the analysis of gene expression within specific cell types, using markers based on Fluorescent Protein expression for flow sorting these cells, and microarray platforms for analysis of their transcriptional activities and protein complements. Current interests include applications of highly parallel platforms for transcript and protein profiling of minimal sample sizes, and for analysis of genetic and epigenetic mechanisms that regulate gene expression during normal development and in diseased states, specifically pancreatic cancer. He is also funded to study factors involved in the regulation of bud dormancy in Vitis vinifera, and has interests in biodiversity and improvement of third-world agriculture. He has published more than 180 scholarly research articles, holds several patents, was elected a Fellow of the American Association for Advancement of Science in 2002, and serves on the editorial board of Cytometry Part A. He is widely sought as a speaker, having presented over 360 seminars in academic, industrial and conference settings. He was elected Secretary of the International Society for Advancement of Cytometry in 2016. Keywords: Plant and Animal Cellular Engineering; Biological Instrumentation; Flow Cytometry and Sorting

Publications

Jay, E., Harkins, K. R., Galbraith, D. W., & Bohnert, H. J. (1990). Developmentally regulated systemic endopolyploidy in succulents with small genomes. Science, 250(4977), 99-101.

Abstract:

Nuclei from Mesembryanthemum crystallinum (ice plant) exhibit multiple levels of ploidy in every tissue as revealed by flow microfluorometric analysis of isolated nuclei stained with mithramycin. Multiples of the haploid nuclear genome complement (1C) corresponding to 2C, 4C, 8C, 16C, 32C, and 64C were observed. The distribution of nuclei among the different ploidy levels is tissue-specific and in leaves is characteristic of the stage of development. This type of genome organization has been identified in eight other succulent CAM (crassulacean acid metabolism) plant species with small genomes. Multiploidy may be a common property of this type of plant.

Miyazaki, S., Fredricksen, M., Hollis, K. C., Poroyko, V., Shepley, D., Galbraith, D. W., Long, S. P., & Bohnert, H. J. (2004). Transcript expression profiles of Arabidopsis thaliana grown under controlled conditions and open-air elevated concentrations of CO 2 and of O 3. Field Crops Research, 90(1), 47-59.

Abstract:

Microarrays have significantly enhanced our ability to track transcripts and changes in gene expression under different conditions and environments. In order to find determinants of plant performance influenced by atmospheric changes, we tracked transcript profiles in Arabidopsis thaliana (L.) Heynh. grown in a field within SoyFACE. This facility (http://www.soyface.uiuc.edu/ index.htm) consists of a series of open-air rings within which either [CO 2] or [O 3] are elevated above current atmospheric concentrations by 1.5× and 1.2×, respectively. A microarray platform including ∼26,000 DNA elements was used to monitor transcript abundance and changes due to exposure to elevated [CO 2] and [O 3]. Transcripts from plants in growth chambers were further compared with material from plants grown in Free Air Concentration Enrichment (FACE) rings under ambient conditions. Most changes in gene expression were observed between growth chamber and ambient field conditions. Two to four times the number of transcripts were either up- or down-regulated between controlled versus field ambient conditions compared with high versus low [CO 2] or [O 3] contrasts. The differences showed a preponderance of regulated transcripts in categories such as chaperones and general defense reactions, altered (secondary) metabolic functions, redox control, energy provision, protein turnover, signaling and transcription. We discuss the results obtained in a model non-crop plant for their possible relevance in studies with crop species. © 2004 Elsevier B.V. All rights reserved.

Bak, S., Tax, F. E., Feldmann, K. A., Galbraith, D. W., & Feyereisen, R. (2001). CYP83B1, a cytochrome P450 at the metabolic branch paint in auxin and indole glucosinolate biosynthesis in Arabidopsis. PLANT CELL, 13(1), 101-111.
Zhang, X., Zhang, L., Dong, F. C., Gao, J. F., Galbraith, D. W., & Song, C. P. (2001). Hydrogen peroxide is involved in abscisic acid-induced stomatal closure in Vicia faba. PLANT PHYSIOLOGY, 126(4), 1438-1448.
Harkins, K. R., & Galbraith, D. W. (1987). Factors governing the flow cytometric analysis and sorting of large biological particles. Cytometry, 8(1), 60-70.