Anna Glasgow Karls
Associate Professor of Microbiology
Ph.D. (1986) University of Wisconsin, Madison
Phone: 706-583-0822
Email: akarls@uga.edu

Research Interests
The research in my laboratory is on DNA rearrangements that regulate gene expression. We have identified a unique family of DNA recombinases, the Piv/MooV family that includes site-specific recombinases and transposases. We utilize genetic and biochemical approaches to determine recombination mechanisms for the Piv/MooV DNA recombinases. Our current work focuses on the two defining members of the Piv/MooV family. Piv, a site-specific recombinase, mediates inversion of a chromosomal segment that controls expression of virulence factors in the human eye pathogen, Moraxella lacunata. MooV, a DNA transposase, catalyzes reversible excision of the transposable element IS492, which regulates extracellular polysaccharide expression in the marine biofilm-forming bacterium, Pseudoalteromonas atlantica. Definition of the molecular mechanisms for DNA recombination mediated by the recombinases of the Piv/MooV family will significantly contribute to understanding the numerous uncharacterized DNA rearrangements that are involved in medically important processes, ranging from microbial pathogenesis to oncogenesis, and may provide new targets for development of therapeutics.
  • Skaar E.P., LeCuyer B., Lenich A.G., Lazio M.P., Perkins-Balding D., Seifert H.S. and A.C. Karls. 2005. Analysis of the Piv recombinase-related gene family of Neisseria gonorrhoeae. Journal of Bacteriology 187: 1276-1286.
  • Buchner J.M., Robertson A.E., Poynter D.J., Denniston S.S. and A.C. Karls. 2005. Piv site-specific invertase requires a DEDD motif analogous to the catalytic center of the RuvC Holliday junction resolvases. Journal of Bacteriology 187: 3431-3437.
  • Tobiason D.M., Buchner J.M., Thiel W.H., Gernert K.M. and A.C. Karls. 2001. Conserved amino acid motifs from the novel Piv/MooV family of transposases and site-specific recombinases are required for catalysis of DNA inversion by Piv. Molecular Microbiology 39: 641-651.
  • Perkins-Balding D., Duval-Valentin G. and A.C. Glasgow. 1999. Excision of IS492 requires flanking target sequences and results in circle formation in Pseudoalteromonas atlantica. Journal of Bacteriology 181: 4937-4948.
  • Tobiason D.M., Lenich A.G. and A.C. Glasgow. 1999. Multiple DNA binding activities of the novel site-specific recombinase, Piv, from Moraxella lacunata. Journal of Biological Chemistry 274: 9698-9706.
  • Heinrich D.W. and A.C. Glasgow. 1997. Transcriptional regulation of type 4 pilin genes and the site-specific recombinase gene, Piv, in Moraxella lacunata and Moraxella bovis. Journal of Bacteriology 179: 7298-7305.
  • Perkins-Balding D., Dias D.P. and A.C. Glasgow. 1997. Location, degree, and direction of DNA bending associated with the Hin recombinational enhancer sequence and Fis-enhancer complex. Journal of Bacteriology 179: 4747-4753.
  • Lenich A.G. and A.C. Glasgow. 1994. Amino acid sequence homology between Piv, an essential protein in site-specific DNA inversion in Moraxella lacunata, and transposases of an unusual family of insertion elements. Journal of Bacteriology 176: 4160-4164.
  • Marrs C.F., Rozsa F.W., Hackel M., Stevens S.P. and A.C. Glasgow. 1990. Identification, cloning, and sequencing of Piv, a new gene involved in inverting the pilin genes of Moraxella lacunata. Journal of Bacteriology 172: 4370-4377.
  • Sluka J.P., Horvath S.J., Glasgow A.C., Simon M.I. and P.B. Dervan. 1990. Importance of minor-groove contacts for recognition of DNA by the binding domain of Hin recombinase. Biochemistry 29: 6551-6561.
  • Glasgow A.C., Miller J.L. and M.M. Howe. 1990. Bacteriophage Mu sites and functions involved in the inhibition of lambda::mini-Mu growth. Virology 177: 95-105.
  • Glasgow A.C., Bruist M.F. and M. I. Simon. 1989. DNA-binding properties of the Hin recombinase. Journal of Biological Chemistry 264: 10072-10082.
  • Johnson R.C., Glasgow A.C. and M. I. Simon. 1987. Spatial relationship of the Fis binding sites for Hin recombinational enhancer activity. Nature 329: 462-465.
  • Bruist M.F., Glasgow A.C., Johnson R.C., and M.I. Simon. 1987. Fis binding to the recombinational enhancer of the Hin DNA inversion system. Genes and Development 1: 762-772.
  • “Novel Mechanisms for DNA Inversion and Transposition”, NIH