Director, Rat Resource and Research Center (RRRC) (www.rrrc.us)
M.S. Microbiology – Rutgers University/University of Medicine & Dentistry of NJ
Ph.D, Rutgers University/University of Medicine & Dentistry of NJ
Postdoctoral Training: Molecular Genetics - Wadsworth Center, Albany, NY
Building Address: Room N131, 4011 Discovery Drive, Columbia, MO 65203 (Discovery Ridge Research Park)
Phone Number: 573-882-5504
Research Emphasis: Our laboratory takes a comparative medicine approach to studying human disorders by using a variety of animal models of disease. The current emphasis in the lab is on the study of polycystic kidney disease, hereditary deafness, and inflammatory bowel disease. Using both rodent and zebrafish models, we are interested in characterizing disease-causing genes and their protein products in order to elucidate the molecular pathways in which these genes/proteins participate. This knowledge will allow a better understanding of both normal and abnormal development and may ultimately lead to targeted therapeutics. Additionally, we are interested in the generation and characterization of new animal models. Our lab has been involved in efforts to characterize rat embryonic stem cells (ESCs), isolate new rat ESC lines, create and validate a novel rat and zebrafish cell ablation model system and use evolving technologies such as CRISPR/Cas9 to create new genetically engineered rat models. We are currently studying the role of microbiome on animal model phenotypes, including zebrafish models of stress and anxiety.
Teaching Responsibilities: Laboratory Animal Medicine (various courses), VPB 5579: Veterinary Genomics (Course Director), Bio Sc 4982/7982: Human Genetics (Course Director), LAB AN 9476: Grant and Manuscript Writing (Course Director).
Davis, D.J., Klug, J., Hankins, M., Doerr, H.M., Monticelli, S.R., Song, A., Hagan, C.E., Bryda, EC. Clove Oil Reduces Serum Cortisol Levels During Euthanasia and Increases Blood Collection Efficiency in Danio rerio. JAALAS 54:564-567 (2015).
Ericsson, A.C., Akter, S., Hanson, M.M., Busi, S.B., Parker, T.W., Schehr, R.J., Hankins, M.A., Ahner, C.E., Davis, J.W., Franklin, C.L., Amos-Landgraf, J.M., Bryda E.C. Differential Susceptibility to Colorectal Cancer due to Naturally Occurring Gut Microbiota. Oncotarget 6:33689-33704 (2015).
Taskiran, E.Z., Korkmaz, E., Gucer, S., Kosukcu, C., Kaymaz, F., Koyunlar, C., Bryda, E.C., Chaki, M., Lu, D., Vadnagara, K., Candan, C., Topaloglu, R., Schaefer, F., Attanasio, M., Bergmann, C., Ozaltin, F. Mutations in ANKS6 Cause a Nephronophthisis-Like Phenotype with ESRD. J Am Soc Nephrol. 25:1653-1661 (2014).
Bock, A.S., Leigh, N.D., Bryda, E.C. Effect of Gsk3 inhibitor CHIR99021 on aneuploidy levels in rat embryonic stem cells. In Vitro Cell Dev Biol Anim. 50:572–579 (2014).
Men, H. and Bryda, E.C. Derivation of a Germline Competent Transgenic Fischer 344 Embryonic Stem Cell Line. PLoS One 8:e56518 (2013).
Men, H., Bauer, B.A., Bryda, E.C. Germline Transmission of a Novel Rat Embryonic Stem Cell Line Derived From Transgenic Rats. Stem Cells and Development 21:2606-2612 (2012).
Bryda, E.C., Johnson, N.T., Ohlemiller, K.K., Besch-Williford, C.L., Moore, E., Bram, R.J. Conditional Deletion of Calcium-modulating Cyclophilin Ligand Causes Deafness in Mice. Mamm Genome 23:270-276 (2011).
Hillhouse A., Taylor J., Bryda E.C., Myles M. and Franklin C.F. Identification of quantitative trait loci on mouse Chromosome 3 and 17. Mamm Genome 22:544–555 (2011).
McElroy J.A., Bryda E.C., McKay, S.D., Schnabel R.D., Taylor J.F. Genetic Variation at a Metallothionein 2A Promoter Single Nucleotide Polymorphism in White and Black females. Journal of Toxicology and Environmental Health, Part A 73:1283-1287 (2010)
Bouvrette, D.J., Sittaramane, V., Heidel, J.R., Chandrasekhar, A., Bryda, E.C. Knockdown of Bicaudal C in Zebrafish (Danio rerio) Causes Cystic Kidneys: A Non-Mammalian Model of Polycystic Kidney Disease. Comparative Medicine 60:96-106 (2010).
Bryda, E.C. and Bauer, B.A. Chapter 20: A Restriction Enzyme-PCR-Based Technique to Determine Transgene Insertion Sites. In “Methods in Molecular Biology, Rat Genomics: Gene identification, Functional Genomics and Model Applications.” I. Anegon (ed). Humana Press, Totowa, NJ. Methods Mol Biol. 597:287-299 (2010).
Black, J., Dykes, A., Thatcher, S., Brown, D., Bryda, E.C., Wright, G.L. FRET Analysis of Actin/Myosin Interaction in Contracting Aortic Smooth Muscle. The Canadian Journal of Physiology and Pharmacology 87: 327-336 (2009).
Stagner, E.E., Bouvrette, D.J., Cheng, J., Bryda, E.C. The Polycystic Kidney Disease-related Proteins Bicc1 and SamCystin Interact. Biochemical and Biophysical Research Communications 383: 16-21 (2009).
Bryda, E.C. and Riley, L.K. Multiplex Microsatellite Markers Panels for Genetic Monitoring of Common Rat Strains. Journal of the American Association for Laboratory Animal Science 47: 37-41 (2008).
Bouvrette, D.J., Price, S.J., Bryda, E.C. The K Homology Domains of the Mouse Polycystic Kidney Disease-related Protein, Bicaudal-C (Bicc1) Mediate RNA Binding In Vitro. Nephron Experimental Nephrology 108:27-34 (2008).
Bryda, E.C., Pearson, M., Agca, Y., Bauer, B.A. Method for Detection and Identification of Multiple Chromosomal Integration Sites in Transgenic Animals Created with Lentivirus. Biotechniques 41:715-719 (2006).
Cogswell, C., Price, S. J., Hou, X., Guay-Woodford, L.M., Flaherty, L., Bryda, E. C. Positional cloning of the jcpk/bpk locus of the mouse. Mammalian Genome 14:242-249 (2003).
Bryda, E.C., Kim, H.J., Legare, M.E., Frankel, W., Noben-Trauth, K. High resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and waltzer (v). Genomics 73: 338-342 (2001).
Di Palma, F., Holme, R.H., Bryda, E.C., Belyantseva, I.A., Pellegrino, R., Kachar, B., Steel, K.P., Noben-Trauth, K. Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D. Nature Genetics 27: 103-107 (2001).
Bolz, H., von Brederlow, B., Ramirez, A., Bryda, E.C., Kutsche, K., Nothwang, H-G, Seeliger, M., Cabrera, M. d.C-S., Vila, M.C., Molina, O.P., Gal, A., Kubisch, C. Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D. Nature Genetics 27:108-112 (2001).