个人简介

1987 Ph.D. University of Utah

研究领域

Molecular Biology and Biochemistry

The Segall lab has recently focused on 3 general research topics: the mechanism of site-specific recombination, the identification and characterization of DNA repair inhibitors, and the diversity and lifestyle of bacteriophages. Towards these goals, we employ a variety of tools including biochemistry, genetics, genomics, bioinformatics, various imaging methods, and structural biology. The mechanism of site-specific recombination mediated by the Integrase (Int) protein of bacteriophage l. Site-specific recombination reactions are wide-spread in nature, and perform many functions in cells including control of gene expression, the separation of dimeric bacterial chromosomes to allow their proper segregation to daughter cells, and control of copy number in plasmids and phages. Many temperate bacteriophages use site-specific recombination to integrate their genomes into host cell chromosomes and to excise them prior to resuming the lytic life cycle. In addition, several of these enzymes have been developed as very useful tools for both prokaryotic and eukaryotic genetics. We have used the phage lambda site-specific recombinase Integrase (Int) as a model system to understand the mechanism of protein machines that rearrange DNA. Four Int molecules, helped by accessory proteins, synapse 2 DNA recombination target sites and perform two rounds of DNA cleavage, exchange and ligation to generate and then to resolve a special DNA intermediate known as a Holliday junction. Int cleaves DNA by a type I topoisomerase mechanism, and like DNA topoisomerases, requires no high energy cofactors. The reaction is very efficient and at the same time highly reversible, which has made the trapping of reaction intermediates very difficult. Our goal is to find the determinants of directionality and efficiency in the Int-mediated recombination reactions. This understanding, in addition to its fundamental insights into how molecular machines work, should allow us to develop even better tools for gene targeting and for generating programmed mutations in any biological system. We have used combinatorial chemistry to find inhibitors that block recombination at different steps. We are currently using these inhibitors to probe the geometry and regulatory features of recombination. Development and characterization of DNA repair inhibitors. While characterizing the inhibitors of site-specific recombination described above, we discovered that they are structure-selective ligands that bind to central and conserved intermediates of DNA repair, preferentially Holliday junctions and to a lesser replication fork-like structures. The inhibitors block the resolution or branch migration of Holliday junctions by several structurally and mechanistically distinct enzymes, including RecG and RuvABC. We are using X-ray crystallography studies to understand the interactions of the inhibitors with the Holliday junction substrate. Since these inhibitors differ in structure from all other known ligands of Holliday junctions, their structure will provide new insights applicable to the design of more specific and higher affinity ligands. Genetic analysis is confirming that these inhibitors interfere with DNA repair, and that DNA repair is a viable novel target of antibiotics. During our studies of these inhibitors we discovered another major source of DNA damage, envelope stress. We are pursuing new studies on how damaging the bacterial membrane leads to DNA damage, what type of damage is generated, and what genes and regulatory pathways are called into play to fix this damage. A number of antibiotics appear to have this effect, and our studies are exploring the mechanism of these “side activities” that may augment the killing action of this class of drugs. Diversity of marine bacteriophages. Bacteriophages are the most abundant biological entity, and profoundly affect the dynamics of microbial populations. They influence carbon cycling in the oceans, shuttle genetic information between bacteria and contribute to the evolution of new bacterial pathogens, and act as a selection force in microbial evolution. Together with Forest Rohwer’s lab, we have explored the diversity of bacterial viruses and their life styles in marine environments. Our current interests in this area are to use computational and bioinformatics tools to develop ways of identifying the potential function and evolutionary relationships of the large fraction of genetic information, much of it encoded by bacteriophages, for which there is no current known function.

近期论文

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Seguritan, V., Alves, N., Jr., Arnoult, M., Raymond, A., Lorimer, D., Burgin, A.B., Jr., Salamon, P., Segall, A. M. (2012) Artificial Neural Networks Trained To Detect Viral and Phage Structural Proteins. PLoS Comput Biol 8(8): e1002657. doi: 10.1371/journal.pcbi.1002657. [Download PDF] Orchard S., Rostron J., and Segall A., 2011. Enterobactin synthesis and uptake mutants are hypersensitive to an antimicrobial peptide that limits the availability of iron in addition to blocking Holliday junction. Microbiology. 2011 Nov 17. [Download PDF ] Rideout M., Boldt J., Vahi-Ferguson G., Salamon P., Nefzi A., Ostresh J., Giulianotti M., Pinilla C., Segall A., 2011. Potent antimicrobial small molecules screened as inhibitors of tyrosine recombinases and Holliday junction-resolving enzymes. Mol Divers. 2011 Nov ; 15(4): 989-1005. [Download PDF ] Lino M., Kus J., Tran S., Naqvi Z., Binnington B., Goodman S., Segall A., and Foster D., 2011. A novel antimicrobial peptide significantly enhances acid-induced killing of Shiga toxin-producing Escherichia coli O157 and non-O157 serotypes. Microbiology. 2011 Jun ; 157(Pt 6): 1768-75. Ranjit D., Rideout M., Boldt J., Nefzi A., Ostresh J., Pinilla C., Segall A., 2010. Small molecule functional analogs of peptides that inhibit λ site-specific recombination and bind Holliday junctions. Bioorganic & Medicinal Chemistry Letters 20 (2010) 4531–4534. [Download PDF ] Su L., Wilner D., Segall A., 2010. An Antimicrobial Peptide That Targets DNA Repair Intermediates In Vitro Inhibits Salmonella Growth within Murine Macrophages. Antimicrob. Agents Chemother. 54(5):1888. [Download PDF ] Tsuji, S., I. Naili, N. Authement, V. Hernandez, B. Hancock, M. Giacalone, A. Segall and S. Maloy. 2010. An efficient thermo-inducible bacterial suicide system: Application for elimination of viable parental bacteria from minicells. Bioprocess International. Mobberley J., Authement N., Segall A., Edwards R., Slepecky R., and Paul J., 2009. Lysogeny and Sporulation in Bacillus Isolates from the Gulf of Mexico. Appl. Environ. Microbiol. 2010, 76(3):829. [Download PDF ] Vanhooff V., Normand C., Galloy1 C., Segall A., and Hallet B., 2009. Control of directionality in the DNA strand-exchange reaction catalysed by the tyrosine recombinase TnpI. Nucleic Acids Research;38(6):2044–2056. [Download PDF ] Fujimoto, D.F., Sterba, K., Segall, A., Maleki, S.J., Higginbotham, R.H., Smeltzer, M., Hurlburt, B.K. 2009. Staphylococcus aureus SarA is a Regulatory Protein Responsive to Redox and pH that Can Support Bacteriophage Lambda Integrase Mediated Excision/Recombination. Molecular Microbiology. 74(6):1445-58. [Download PDF ] Gunderson CW, Boldt JL, Authement RN, Segall AM, 2009. Peptide wrwycr inhibits the excision of several prophages and traps holliday junctions inside bacteria. J Bacteriol. Apr;191(7):2169-76. [Download PDF] Kepple KV, Patel N, Salamon P, Segall AM, 2008. Interactions between branched DNAs and peptide inhibitors of DNA repair. Nucleic Acids Res. Sep;36(16):5319-34. [Download PDF] Garcia-Russell N, Orchard SS, Segall AM, 2007. Probing nucleoid structure in bacteria using phage lambda integrase-mediated chromosome rearrangements. Methods Enzymol. 421:209-26. [Download PDF] Boldt Jeffrey L., Kepple Kevin V., Cassell Geoffrey D. and Segall Anca M., 2007. Spermidine biases the resolution of Holliday junctions by phage lambda integrase. Nucleic Acids Res. 35(3):716-27. [Download PDF] Fujimoto David F., Pinilla Clemencia, and Segall Anca M., 2006. New peptide inhibitors of type IB topoisomerases: similarities and differences vis-a-vis inhibitors of tyrosine recombinases. J. Mol. Biol. 363: 891-907. [Download PDF ] Gunderson Carl and Segall Anca, 2006. DNA repair, a novel antibacterial target: Holliday junction-trapping peptides induce DNA damage and chromosome segregation defects. Mol. Micro. 59 (4), 1129-1148. [Download PDF] Kepple Kevin V., Boldt Jeffrey L., and Segall Anca M., 2005. Holliday junction-binding peptides inhibit distinct junction-processing enzymes. PNAS 102 (19): 6867-6872. [Download PDF] Ghosh Kaushik, Lau Chi Kong, Guo Feng, Segall Anca M., Van Duyne Gregory D., 2005. Peptide trapping of the Holliday junction intermediate in Cre-Lox site-specific recombination. J Biol Chem. Mar 4;280(9):8290-9. [Download PDF] Lovett Susan T., Segall Anca M., 2004. New views of the bacterial chromosome - Symposium on Bacterial Chromosomes. EMBO reports 5:860-864. [Download PDF] Garcia-Russell, Harmon Timothy G., Le Tien Q., Amaladas Nelusha H., Mathewson Richard D., Segall Anca M., 2004. Unequal access of chromosomal regions to each other in Salmonella: probing chromosome structure with phage integrase-mediated long range rearrangements. Mol. Micro. 52: 329-344. [Download PDF] [Erratum]