Brian Condie
Associate Professor
Ph.D. (1989) University of California, Berkeley
Phone: 706-542-1431
Email: bcondie@uga.edu
Dr. Condie is a member of Developmental Biology at UGA

Research Interests
A major goal of the research in my lab is define the genetic pathways that regulate fetal thymus development in mice.  Normal thymus development is necessary for the production of normal T cells - the key components of cellular adaptive immunity in mammals.  We are focused on defining the pathways that regulate the differentiation of thymic epithelial cells (TECs) from the pharyngeal endoderm.  TECs provide the  microenvironment that is required for normal T cell production from lymphoid progenitor cells.  Although TECs play a critical role in normal T cell production there is relatively little known about their normal development.  To address this gap in knowledge my lab has recently identified several candidate transcription factors that are involved in TEC differentiation and genetic studies of these factors in mice are underway.  The genes we are identifying are candidates for loci involved in causing T cell immunodeficiencies or dysfunction.  They will also be important for future studies of thymus aging and regeneration.

I also have a strong interest in developing new genetic research tools that are based on site-specific recombination.  Site-specific recombinases are used to generate tissue specific genetic modifications in mice and other systems.  I am focused on developing new approaches for tissue or cell type restricted activation of site-specific recombinases in developing and adult mice as well as in cultured stem cells.

  • Guo, T., K. Mandai, B.G. Condie, R.S. Wickramasinghe, M.R. Capecchi and D.D. Ginty. 2010. An evolving NGF-Hoxd1 signaling pathway mediates development of divergent neural circuits in vertebrates. Nature Neuroscience in press.
  • Manley, N.R. and B.G. Condie. 2010. Transcriptional regulation of thymus organogenesis and thymic epithelial cell differentiation. Progress in Molecular Biology and Translational Science 92C: 103-120.
  • Chen, L., P. Zhao, L. Wells, C.T. Amemiya, B.G. Condie and Manley, N.R. 2010. Mouse and zebrafish Hoxa3 orthologs have non-equivalent in vivo protein function. PNAS 107: 10555-10560.
  • Oh, W.-J., J.J. Westmoreland, R. Summers and B.G. Condie. 2010. Cleft palate and body wall defects are caused by CNS dysfunction in Gad1 and Viaat knockout mice. PLoS One 5: e9758.
  • Urbanski, W.M. and B.G. Condie. 2009. Textpresso Site-Specific Recombinases: a text-mining server for the recombinase literature including Cre mice and conditional alleles. Genesis 47: 842-846.
  • Lee J.M., J. Tiong, D.M. Maddox, B.G. Condie and S. Wray. 2008. Temporal migration of GnRH-1 neurones is modified in GAD67 knockout mouse. J. Neuroendocrinology 20: 93-103.
  • Gordon, J., B. Hughes, D.-M. Su, S. Xiao, S.P. Navarre, B.G. Condie and N.R. Manley. 2007. Specific expression of lacZ and Cre recombinase in fetal thymic epithelial cells by multiplex gene targeting at the Foxn1 locus. BMC Developmental Biology 7: 69.
  • Noggle, S.A., D. Weiler and B.G. Condie. 2006. NOTCH signaling is inactive but inducible in human embryonic stem cells. Stem Cells 24: 1646-1653.
  • Oh, W.-J., S.A. Noggle, D.M. Maddox and B.G. Condie. 2005. The mouse Viaat/Vgat gene: expression during embryogenesis, analysis of its core promoter in neural stem cells and a reconsideration of its alternate splicing. Gene 351: 39-49.
  • Bieberich, E., J. Silva, G. Wang, K. Krishnamurthy and B.G. Condie. 2004. Selective apoptosis of pluripotent mouse and human stem cells by novel ceramide analogs prevents teratoma formation and enriches for neural precursors in ES-cell derived neural transplants. J. Cell Biology 167: 723-734.
  • "A new site specific recombinase for mammalian genome engineering," NIH
  • "Foxn1 and Molecular Mechanism of Thymic Involution," NIH