Karl J. Franek, PhD

 Contacts | Site Index

Search GGC Website

 

864-388-1044 (voice)

864-388-1808 (fax)

kfranek@ggc.org

Staff Scientist

  • B.Sc. (Biology, Honors) University of Windsor, Canada, 1984
  • B.Ed (Biology, Chemistry) Queen’s University, Canada, 1990
  • M.Sc. (Biology) University of Windsor, Windsor, Ontario, Canada
  • Ph.D. (Microbiology and Immunology), Louisiana State University Health Sciences Center, 1998
  • Postdoctoral Fellow, Department of Microbiology and Immunology, LSU Health Sciences Center, 1998-1999
  • Postdoctoral Fellow/Research Associate, Department of Biological Sciences, Clemson University and the Oncology Research Institute, Greenville Hospital System, 1999-2004
  • Staff Scientist, Center for Molecular Studies, JC Self Research Institute of Human Genetics, Greenwood Genetic Center, October 2004- present
Dr. Franek’s research focuses on the functional aspects of the genes associated with X-linked Mental Retardation (XLMR) and Split Hand/Foot Malformation (SHFM). His studies apply molecular and cellular methods to elucidate the role of these genes in cellular functions such as cell-to-cell adhesion, migration, cell signaling and gene regulation.

These investigations of XLMR genes will shed light on their role in the cause of various phenotypic characteristics in XLMR patients. A better understanding of the function of these genes at the cellular level may lead to potential therapeutic strategies directed to the treatment of XLMR. Dr. Franek’s group carries out functional studies of XLMR genes in primary and cultured neuronal cells, and examines the effects of mutations in these genes on neural development during differentiation in mouse embryonic stem cells.

Dr. Franek is currently studying the function of several genes with mutations in patients with various forms of XLMR including:

  • XAP5
  • Renin receptor (Atp6ap2) (X-linked MR with Epilepsy; XLMRE)
  • Fgd1, a Rho/Rac guanine nucleotide exchange factor containing the zinc finger FYVE that is associated with faciogenital dysplasia (Aarskog-Scott Syndrome)
  • Dlg3 (Discs, large homolog 3)/SAP102 (synapse-associated protein 102) involved in XLMR.
  • The monocarboxylate transporter MCT8 (SLC16A2), a specific transporter of thyroid hormone that has been implicated in Allan-Herndon-Dudley Syndrome (AHDS).

Dr. Franek also works in association with other members of the Research Institute, as well as members of the Diagnostic Laboratories at GGC, in the design of molecular and cellular studies of gene function.

In addition, in collaboration with Dr. Lesly A. Temesvari of Clemson University, Dr. Franek employs the myxomycete Dictyostelium discoideum (cellular slime mold) as a model system to identify potential new roles for the function of XLMR genes and their homologs during the developmental life cycle of Dictyostelium.

Selected Publications:

  • North MJ, Cotter DA, Franek KJ. Dictyostelium discoideum spore germination: Increases in proteinase activity are not directly coupled to the emergence of myxamoebae. Journal of General Microbiology 136:835-840, 1990.
  • North MJ, Franek KJ, Cotter DA. Differential secretion of Dictyostelium proteinases. Journal of General Microbiology 136:827-833, 1990.
  • North MJ, Cotter DA, Franek KJ. Cysteine proteinase changes during microcyst formation and germination in Polysphondylium pallidum. Current Microbiology 22:59-63, 1991.
  • North MJ, Cotter DA, Franek KJ. Cysteine proteinase changes during macrocyst formation in Dictyostelium mucoroides. FEMS Letters 72:153-158, 1991.
  • Bush J, Franek K, Cardelli J. Cloning and characterization of seven novel Dictyostelium discoideum rac-related genes belonging to the rho family of GTPases. Gene 136:61-68, 1993.
  • Bush J, Franek K, Daniels J, Spiegelman G, Weeks G, Cardelli J. Cloning and characterization of five novel Dictyostelium discoideum rab-related genes. Gene 136:55-60, 1993.
  • Franek KJ, Wolcott RM, Chervenak R. Reliable method for the simultaneous detection of cytoplasmic and surface CD3 expression by murine lymphoid cells. Cytometry 17:224-236, 1994.
  • Lybarger L, Dempsey D, Franek KJ, Chervenak R. Rapid generation and flow cytometric analysis of stable GFP-expressing cells. Cytometry 25:211-220, 1996.
  • Franek KJ, Chervenak R. Progenitor cell seeding of the thymus: a wide window of opportunity. Current Trends in Immunology 1:29-39, 1998.
  • Franek KJ, Chervenak R. Simultaneous detection of cytoplasmic and surface expression of CD3 proteins by flow cytometry. In: Protocols in T cell Development and Activation, Methods in Molecular Biology Series, Humana Press, K.P. Kearse, ed., vol. 134, pp. 103-116, 2000.
  • Li J, Holmes LM, Franek KJ, Sticca RP, Wagner TE, Wei Y. Murine tyrosinase expressed by a T7 vector in bone marrow-derived dendritic progenitors effectively prevents and eradicates melanoma tumors in mice. Cancer Gene Therapy 7(11):1448-55, 2000.
  • Li J, Holmes LM, Franek KJ, Burgin KE, Wagner TE, Wei Y. Purified hybrid cells from dendritic cell and tumor cell fusions are superior activators of antitumor immunity. Cancer Immunol Immunother 50:456-462, 2001.
  • Beck MT, Chen NY, Franek KJ, Chen WY. Prolactin Antagonist Endostatin Fusion Protein as Targeted Dual Functional Therapeutic Agent for Breast Cancer. Cancer Research 63:3598-3604, 2003.
  • Li J, Franek KJ, Patterson AL, Holmes LM, Burgin KE, Ji J, Yu X, Wagner TE, Wei Y. Targeting foreign major histocompatibility complex (MHC) molecules to tumors by tumor cell-specific single chain antibody (scFv). Int. J. Oncology 23:1329-1332, 2003.
  • Franek KJ, Zhou Z, Zhang W-D, Chen WY. In vitro studies of baicalin alone or in combination with Salvia miltiorrhiza as a potential anti breast cancer agent. Int J Oncol 26(1):217-24, 2005.

 

 

Clinical Services | Diagnostic Services | Education Division | Research | Faculty | Biotechnology | South Carolina Birth Defects Foundation

Home | Contacts | Directions/Maps | Site Index

 

Greenwood Genetic Center

101 Gregor Mendel Circle, Greenwood, SC  29646

864-941-8100; 888-GGC-GENE (442-4363)

webmaster@ggc.org