The overall goal of this proposal is to gain insight into the relationships among DNA structure, trans-acting factors, protein- nucleic acid interactions, and the regulation of gene transcription in plants. The experiments involve the maize alcohol dehydrogenase genes. Adhl and Adh2 exhibit differential tissue specificity, yet anaerobiosis mediates the coordinate transcriptional expression of both Adh genes. This provides a unique opportunity to evaluate the roles played by trans-acting factors and protein-nucleic acid interactions in the activation of two closely related genes, and to compare and contrast the developmental and environmental activation of gene transcription. The main focus of this rather straightforward proposal is the in vitro characterization and purification of the trans-acting protein factors that affect the regulation of the Adh genes. While this general area of research has been actively pursued in animal systems, plant trans-acting factors are only now beginning to be investigated. What makes this proposal particularly feasible and appropriate is that we already know (at least some of) the factors involved in Adh regulation. From our in vivo footprinting studies we know the binding sites of at least four regulatory factors, and we know their dimethyl sulfate footprint signatures. Therefore we know precisely the factors we are searching to purify and are not simply looking for proteins that (just) bind to Adh DNA.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM040061-04
Application #
3297360
Study Section
Molecular Cytology Study Section (CTY)
Project Start
1989-01-01
Project End
1993-12-31
Budget Start
1992-01-01
Budget End
1992-12-31
Support Year
4
Fiscal Year
1992
Total Cost
Indirect Cost
Name
University of Florida
Department
Type
Schools of Arts and Sciences
DUNS #
073130411
City
Gainesville
State
FL
Country
United States
Zip Code
32611
Paul, A L; Ferl, R J (1999) Higher-order chromatin structure: looping long molecules. Plant Mol Biol 41:713-20
Paul, A L; Ferl, R J (1998) In vivo footprinting in Arabidopsis. Methods Mol Biol 82:417-29
Paul, A L; Ferl, R J (1998) Permeabilized Arabidopsis protoplasts provide new insight into the chromatin structure of plant alcohol dehydrogenase genes. Dev Genet 22:7-16
Paul, A L; Ferl, R J (1998) Higher order chromatin structures in maize and Arabidopsis. Plant Cell 10:1349-59
Wu, K; Rooney, M F; Ferl, R J (1997) The Arabidopsis 14-3-3 multigene family. Plant Physiol 114:1421-31
Lu, G; Paul, A L; McCarty, D R et al. (1996) Transcription factor veracity: is GBF3 responsible for ABA-regulated expression of Arabidopsis Adh? Plant Cell 8:847-57
Rooney, M F; Ferl, R J (1995) Sequences of three Arabidopsis general regulatory factor genes encoding GF14 (14-3-3) proteins. Plant Physiol 107:283-4
Laughner, B; Lawrence, S D; Ferl, R J (1995) Two cDNA clones encoding 14-3-3 homologs from tomato fruit. Biochim Biophys Acta 1263:67-70
Ferl, R J; Lu, G; Bowen, B W (1994) Evolutionary implications of the family of 14-3-3 brain protein homologs in Arabidopsis thaliana. Genetica 92:129-38
de Vetten, N C; Ferl, R J (1994) Two genes encoding GF14 (14-3-3) proteins in Zea mays. Structure, expression, and potential regulation by the G-box binding complex. Plant Physiol 106:1593-604

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