Fayth K. Yoshimura, PhD
Professor
6257 Scott Hall
(313) 577-1571
fyoshi@med.wayne.edu
Fayth K. Yoshimura, Ph.D., is Associate Professor of Immunology and Microbiology. She received her Ph.D. from Yale University in 1972. She was a post-doctoral fellow at the Massachusetts Institute of Technology and Research Assistant and Associate Professor at the University of Washington prior to coming to Wayne State University in 1995.

Dr. Yoshimura's research interests include the study of tumorigenesis by murine retroviruses, and porcine retroviruses and their potential pathogenesis in xenotransplantation. To elucidate the mechanism by which murine retroviruses cause T cell tumors, her laboratory has focused on the regulation of transcription of cellular oncogenes by retroviral sequences. She has identified binding sites for transcription factors in the long terminal repeat region of the virus that regulate transcription in a T cell-specific manner. Some of these sites have been shown to be important for tumorigenesis by these viruses. Her research includes studies of the ability of oncogenic murine retroviruses to induce apoptosis of thymic lymphocytes. The methodology involved in her laboratory includes DNA footprinting, gel mobility shift assays, site-directed mutagenesis, transfection of mammalian cells, reporter gene assays, flow cytometry, and assays for apoptosis. Questions her laboratory is currently pursuing include the 1). Identification of proteins that bind to transcriptional regulatory sites; 2). Isolation of these proteins and cloning of the genes that encode them; 3). Determination of how these proteins interact with promoter sequences to regulate transcription; 4). Identification of the cell type in the thymus that is involved in tumorigenesis and apoptosis.

Her work with porcine retroviruses includes the identification of viruses which are able to infect human cells and tissues. Questions that are currently being pursued in this area of research include: 1). Whether various pig tissues and organs either already in use or being considered for human transplantation express retroviruses; 2). Which human tissues and organs are infectable by these retroviruses; 3). How can viral replication in human tissues be prevented.

Selected Publications
Baxa D.M., Luo X., Yoshimura F.K. Genistein induces apoptosis in T lymphoma cells via mitochondrial damage. Nutr. Cancer., 51:93-101, 2005. Medline
Nanua S., Yoshimura F.K. Mink epithelial cell killing by pathogenic murine leukemia viruses involves endoplasmic reticulum stress. J. Virol., 78:12071-12074, 2004. Medline
Nanua S, Yoshimura FK. Differential cell killing by lymphomagenic murine leukemia viruses occurs independently of p53 activation and mitochondrial damage. J. Virol., 78:5088-96, 2004. Medline
Baxa DM, Yoshimura FK. Genistein reduces NF-kappa B in T lymphoma cells via a caspase-mediated cleavage of I kappa B alpha. Biochem. Pharmacol., 66:1009-1018, 2003. Medline
Wilson CA, Laeeq S, Ritzhaupt A, Colon-Moran W, Yoshimura FK. Sequence analysis of porcine endogenous retrovirus long terminal repeats and identification of transcriptional regulatory regions. J. Virol., 77:142-149, 2003. Medline
Yoshimura, F. K., T. Wang, and S. Nanua. 2001. Mink cell focus-forming murine leukemia virus killing of mink cells involves apoptosis and superinfection. J. Virol., 75:6007-6015. Medline
Yoshimura, F.K. and T. Wang. 2001. Role of the LTR region between the enhancer and promoter in mink cell focus-forming murine leukemia virus pathogenesis. Virology, 283:121-131. Medline
Yoshimura, F.K., T. Wang, F. Yu, H-R Kim, and J. Turner. 2000. Mink cell focus-forming murine leukemia virus infection induces apoptosis of thymic lymphocytes. J. Virol. 74:8119-8126. Medline
Yoshimura, F. K., T. Wang, and M. Cankovic. 1999. Sequences between the enhancer and promoter in the long terminal repeat affect murine leukemia virus pathogenicity and replication in the thymus. J. Virol. 73:4890-4898. Medline
Chen, H. and F.K. Yoshimura. 1998. Spacing between the enhancer and promoter of the long terminal repeat of a murine retrovirus is required for transcriptional activation in T cells. J. Gen. Virol. 79:1101-1104. Medline
Yoshimura, F. K., M. Cankovic, R. Smeltz, and S. Ibrahim. 1997. Identification of nucleotide sequences that regulate transcription of the MCF13 murine leukemia virus long terminal repeat in activated T cells. J. Virol. 71:2572-2576. Medline
Yoshimura, F.K., K. Diem, G. H. Learn, Jr., S. Riddell, and L. Corey. 1996. Intrapatient sequence variation of the gag gene of human immunodeficiency virus type 1 plasma virions. J. Virol. 70:8879-8887. Medline
Yoshimura, F. K. and K. Diem. 1995. Characterization of nuclear protein binding to a site in the long terminal repeat of a murine leukemia virus:comparison with the NFAT complex. J. Virol. 69:994-1000. Medline

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