Areas of Interest
- DNA binding and bending proteins
- Role of DksA in cellular response to nutritional stress
- Role of Fis in E. coli
- Genes subject to Fis regulation
- Mechanisms of Fis regulation
Our current work involves the regulation of DksA in E. coli. Bacteria rely on numerous global gene regulators to rapidly control the activity of many of its genes in their attempt to protect themselves or benefit from a sudden change in their immediate environment. DksA, a fairly recently discovered bacterial gene regulator, plays an essential role in the regulation of the transcription of ribosomal RNA (necessary for the synthesis of proteins in the cell) and of numerous other genes involved in a variety of important cellular processes. DksA differs from most bacterial gene regulators in that it functions by binding directly to the RNA polymerase enzyme (the enzyme responsible for carrying out transcription) rather than to DNA. Little is known about how DksA itself is regulated. Therefore, this project focuses on attaining a detailed understanding of how Escherichia coli cells control the production of DksA in response to different growth conditions. Preliminary work indicated that the dksA gene is regulated at the level of transcription (i.e RNA synthesis). The regulation involves two transcription initiation sites (i.e. promoters), and several other transcription factors (including DksA itself). The dksA gene expression was also found to be controlled at the level of translation (i.e. protein synthesis), and this control required a specific portion of the dksA mRNA referred to as the 5’-untranslated region (5’-UTR). One aim of this project is to investigate how dksA is transcriptionally controlled under various different growth conditions. The dksA promoters, including a newly discovered promoter, which is most active under conditions of starvation, will be more precisely defined. The dksA regulatory effects by several suspected transcription factors will be investigated in detail. The relative transcription activity from all dksA promoters will be simultaneously measured while in their native chromosomal contexts during different growth conditions and in different bacterial strains lacking any of suspected transcriptional regulators. Another aim is to investigate how dksA gene expression is controlled at a post-transcriptional step (i.e. after the dksA mRNA has been made). The project will examine the hypothesis that changes in the rate of breakdown of dksA mRNA during different phases of cell growth contribute to the regulation of dksA expression. The relative DksA protein levels in various E. coli strains and several other bacterial species will be measured during different growth conditions. The effects of suspected dksA transcription regulators on the cellular levels of DksA protein will also be examined. The PI will probe the RNA structure in the 5’-UTR of the dksA mRNA and carefully examine its role in translation control. The project will also aim to detect, capture, and identify potential cellular factors that may associate with the 5’-UTR to affect translation control of DksA. Together, these experiments will provide a broad and extensive understanding of the cellular processes used to regulate this important global gene regulator in response to different bacterial growth conditions.
Our lab has had a longstanding interest in studying some of the functions of the DNA binding and bending protein Fis in E. coli,as well as understanding the mechanisms involved in its growth phase-specific regulatory pattern. Fis (Factor for Inversion Stimulation) is involved in several different biological processes such as stimulation of DNA inversion reactions mediated by the Hin, Gin, and Cin family of recombinases, stimulation of lambda phage DNA integration and excision from the bacterial chromosome, stimulation of transcription of ribosomal and tRNA operons and other genes, autoregulation and repression of several other genes, and modulation of DNA topology.
Fis is subject to a complex set of transcriptional control mechanisms. Together, they allow adequate Fis expression levels in response to sudden changes in the nutritional environment. Upon a nutitional upshift, Fis protein and mRNA levels rapidly increase, reaching a peak within the time that is required for the cells to shift to a faster growth rate, and then decreases to very low or undetectable levels during late logarithmic growth and early stationary phases. Understanding the molecular mecahnism(s) responsible for this peculiar growth phase-dependent regulation pattern is a subject of investigation in our lab. Fis is also subject to negative trasncriptional control in response to conditions of starvation, otherwise known as stringent control. We have shown that stringent control and growth phase-dependent regulation require different and separable molecular mechanisms. Between the two, levels of Fis mRNA become tightly coupled to the nutritional environment. Two additional mecahnisms of transcriptional control include stimulation by the integration host factor (IHF) and transcriptional repression by Fis. The IHF protein binds to a site centered at about 116 bp upstream of the fispromoter transcriptional start site to stimulate transcription three to four-fold. The transcription stimulation occurs in a helical phasing-dependent manner, suggesting that its action may require an interaction with the promoter-bound RNA polymerase. Negative regulation by Fis requires at least two Fis binding sites that flank the fiscore promoter region. Because neither the stringent control, IHF stimulation, or the Fis auteoregulation are required for the growth-phase-dependent regulation observed for Fis, and because the fiscore promoter region is sufficient to generate its growth phase regulation pattern, we have focused on the fiscore promoter region to more closely investigate the molecular details surrounding this process. Thus far, we have been able to link the growth phase dependent control with the use of a poor match to the -35 and -10 sigma 70 promoter consensus sequences, combined with the use of CTP as the primary transcription initiation nucleotide.
To learn more about the role of Fis in E. coli,we became interested in identifying new genes that are subject to Fis regulation. We have performed 2-dimensional gel electrophoresis and observed that there are a number of proteins (>25) that are more highly expressed in the presence of Fis and another set of proteins that are repressed in the presence of Fis. So far we have been able to identify 9 of them by partial microsequencing. We have also performed DNA microarray analysis and have uncovered many more genes that appear ot be subject to Fis regulation, directly or indirectly. Current research efforts are focusing on Fis as a global gene regulator.
We are also interested in understanding how a Fis dimer specifically interacts with DNA and other proteinsto carry out its functions. Genetic and Biochemical studies have shown that Fis contains at least two functional regions. A carboxy-terminal region (amino acids 74-94) contains a helix-turn-helix DNA binding motif and is required for proper DNA binding and bending. Another region closer to the amino terminus (amino acids 17 to 44) is required for the ability of Fis to stimulate Hin-mediated DNA inversion, but is not required for other functions such as DNA binding, DNA bending, stimulation of lambda DNA excision, and autoregulation.
- Shao, Y., L. S. Feldman-Cohen, and R. Osuna. 2008. Biochemical identification of base and phosphate contacts between Fis and a high-affinity DNA binding site. J. Mol. Biol. 380: 327-339.[abstract]
- Shao, Y., L. S. Feldman-Cohen, and R. Osuna. 2008. Functional characterization of the Escherichia coli Fis-DNA binding sequence. J. Mol. Biol. 376:771-785. [abstract]
- Bradley, M. D., M. B. Beach, A. P. Jason de Koning, T. S. Pratt, and R. Osuna. Effect of Fis on Escherichia coli gene expression during different growth stages. 2007. Microbiology 153:2922-2940. [abstract]
- Mallik, P., B. J. Paul, S. T. Rutherford, R. L. Gourse, and R. Osuna. 2006. DksA is required for growth phase-dependent regulation, growth-rate control, and stringent control of fis expression in Escherichia coli. J. Bacteriol. 188:5775-5782. [abstract]
- Meinhold, D., M. Beach, Y. Shao, R. Osuna, and W. Colón. 2006. The location of an engineered inter-subunit disulfide bond in FIS affects the denaturation pathway and cooperativity. Biochemistry 45:9767-9777. [abstract]
- Feldman-Cohen, L. S., Y. Shao, D. Meinhold. C. Miller, W. Colón, and R. Osuna. 2006. Common and variable contributions of Fis residues to high-affinity binding at different DNA sequences. J. Bacteriol. 188:2081-2095. [abstract]
- Walker, K. A., P. Mallik, T. S. Pratt, and R. Osuna. 2004. The Escherichia coli fis promoter is regulated by changes in the levels of its transcription initiation nucleotide CTP. J. Biol. Chem. 279:50818-50828. [abstract]
- Mallik, P., T. S. Pratt, M. B. Beach, M. D. Bradley, J. Undamatla, and R. Osuna. 2004. Growth phase-dependent regulation and stringent control of fis are conserved processes in enteric bacteria and involve a single promoter ( fis P) in Escherichia coli . J. Bacteriol. 186:122- 135. [abstract]
- Boswell, S., J. Matthew, M. Beach, R. Osuna, and W. Colón. 2004. Variable contributions of tyrosine residues to the structural and spectroscopic properties of the factor for inversion stimulation. Biochemistry 43:2964-2977. [abstract]
- Walker, K.A., and R. Osuna. 2002. Factors affecting start site selection at the Escherichia coli fispromoter. J. Bacteriol. 184:4783-4791. [abstract]
- Hobart, S.A., W. Meinfold, R. Osuna, and W. Colon. 2002. From two-state to three-state: effect of P61A mutation on the dynamics and stability of the factor for inversion stimulation results in na altered equilibrium denaturation mechanism. Biochemistry 41:13744-13754. [abstract]
- Hobart, S.A., S. Ilin, D.F. Moriarty, R. Osuna, and W. Colon. 2002. Equilibrium denaturation studies of the Escherichia coli factor for inversion stimulation: implications for in vivo function. Protein Science 11:1671-1680. [abstract]
- Walker, K.A., C.L. Atkins, and R. Osuna. 1999. Functional determinants of the Escherichia coli fispromoter: roles of -35, -10, and transcription initiation regions in the response to stringent control and growth phase-dependent regulation. J. Bacteriol. 181:1269-1280. [abstract]
- Beach, M.B., and R. Osuna. 1998. Identification and characterization of the fis operon in enteric bacteria. J. Bacteriol. 180:5932-5946. [abstract]
- Pratt, T.S., T. Steiner , L.S. Feldman, K.A. Walker, and R. Osuna. 1997. Deletion analysis of the fispromoter region in Escherichia coli: antagonistic effects of integration host factor and Fis. J. Bacteriol. 179:6367-6377 [abstract]
- Osuna, R., D. Lineau, K. T. Hughes, and R. C. Johnson. 1995. Sequence, regulation, and functions of fis in Salmonella typhimurium. J. Bacteriol. 177: 2021-2032. [abstract]
- Gosink, K. K., W. Ross, S. Leirmo, R. Osuna, S. E. Finkel, R. C. Johnson, and R. L. Gourse. 1993. DNA binding and bending are necessary but not sufficient for Fis-dependent activation of rrnB P1. J. Bacteriol. 175:1580-1589. [abstract]
- Ball, C. A., R. Osuna, K. C. Ferguson, and R. C. Johnson. 1992. Dramatic changes in Fis levels upon nutrient upshift in Escherichia coli. J. Bacteriol. 174:8043-8056. [abstract]
- Osuna, R., S. E. Finkel, and R. C. Johnson. 1991. Identification of two functional regions in Fis: the N-terminus is required to promote Hin-mediated DNA inversion but not lambda excision. EMBO J.10:1593-1603. [abstract]
- Osuna, R., B. K. Janes, and R. A. Bender. 1994. Roles of Catabolite Activator Protein sites centered at -81.5 and -41.5 in the activation of the Klebsiella aerogenes histidine utilization operon hutUH. J. Bacteriol. 176:5513-5524. [abstract]
- Osuna, R., A. Schwacha, and R. A. Bender. 1994. Identification of the hutUH operator (hutUO) from Klebsiella aerogenes by DNA deletion analysis. J. Bacteriol. 176:5525-5529. [abstract]
- Osuna, R. and R. A. Bender. 1991. Klebsiella aerogenes catabolite gene activator protein and the gene encoding it (crp). J. Bacteriol. 173:6626-663. [abstract]
- Osuna, R., S. A. Boylan, and R. A. Bender. 1991. In vitro transcription of the histidine utilization (hutUH) operon from Klebsiella aerogenes. J. Bacteriol. 173:116-123. [abstract]
- Morales, M.H., R. Osuna, and E. Sanchez. 1991. Vitellogenesis in Anolis pulchellus: induction of VTG-like protein in liver explants from male and immature lizards. J. Exp. Zool. 260:50-8. [abstract]