The long term interest of this laboratory lies in understanding the control of gene activity. In depth studies of bacteria and their viruses have long revealed the importance of specific interactions between segments of the chromosome and controlling proteins in governing whether a given gene is expressed. For some time we have develop our efforts to studying the mechanism of gene regulation in the L-arabinose system E. coli. This system has provided us with the first example of positive gene control, and the genetic and biochemical analyses that followed have revealed an intricate pattern of regulation, involving both positive and negative mechanisms. Advances in molecular techniques in gene manipulations, combined with our familiarity with this system, have brought considerable insight into the biochemical events that govern gene activity. The proposed research addresses the molecular interactions between regulatory proteins and DNA, and the mechanisms involved in transcriptional activation. We have utilized methodologies whereby specific regulatory proteins may be added to purified target sites in vitro, and their interactions monitored by a variety of physical, biochemical, and biologic methods. We plan to pursue the study of the mechanism of transcriptional activation at the ara operon promoter by the regulatory proteins AraC and CAP, to compare their modes of action and to test their interdependence. We will also carry out genetic and biochemical dissections of the regulatory protein AraC and its target sites on the DNA. Our goal is to arrive at a better understanding of the molecular mechanisms involved.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM014652-21A1
Application #
3268674
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1978-01-01
Project End
1992-06-30
Budget Start
1988-07-01
Budget End
1989-06-30
Support Year
21
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of California Santa Barbara
Department
Type
Schools of Arts and Sciences
DUNS #
City
Santa Barbara
State
CA
Country
United States
Zip Code
93106
Menon, K P; Lee, N L (1990) Activation of ara operons by a truncated AraC protein does not require inducer. Proc Natl Acad Sci U S A 87:3708-12
Francklyn, C S; Lee, N (1988) AraC proteins with altered DNA sequence specificity which activate a mutant promoter in Escherichia coli. J Biol Chem 263:4400-7
Hamilton, E P; Lee, N (1988) Three binding sites for AraC protein are required for autoregulation of araC in Escherichia coli. Proc Natl Acad Sci U S A 85:1749-53
Lee, N; Francklyn, C; Hamilton, E P (1987) Arabinose-induced binding of AraC protein to araI2 activates the araBAD operon promoter. Proc Natl Acad Sci U S A 84:8814-8
Lichenstein, H S; Hamilton, E P; Lee, N (1987) Repression and catabolite gene activation in the araBAD operon. J Bacteriol 169:811-22
Lee, N; Gielow, W; Martin, R et al. (1986) The organization of the araBAD operon of Escherichia coli. Gene 47:231-44