[return to list
M.  Mitchell  Smith
Degree(s): Ph.D.
Graduate School: Johns Hopkins
Primary Appointment: Professor of Microbiology
Research Interests:
Functional Genomics of Histones, Chromatin, and Protein Acetylation Signaling in Cancer and the Cell Cycle

Email Address: mms7r@virginia.edu


Biomedical Sciences Graduate Program(s)
  • Microbiology, Immunology and Infectious Diseases
  • Biochemistry, Molecular Biology and Genetics

  • Research Description

    My laboratory is interested in the molecular genetics of eukaryotic chromosome structure and function, including the mechanisms of gene transcription, DNA replication, recombination, and chromosome segregation. Our research focuses on the genes that encode the histone proteins which comprise the protein subunits of the nucleosome, the primary building block of the eukaryotic chromosome. Thus, the histones are critical for chromosome structure and dynamics, and their function is required at key steps in the cell division cycle. Our experiments exploit the advanced molecular genetics of the simple eukaryote Saccharomyces cerevisiae, budding yeast. Yeast provides an experimental system that is advantageous for cell biology, biochemistry, and molecular genetic studies. A powerful collection of classical genetic and molecular techniques have been developed for yeast that permit the recombinant DNA cloning and manipulation of genes in vitro and the characterization of new mutants in vivo. Currently, we are focusing on four main research questions: The roles of the histone amino-terminal tail domains in chromatin structure and function, particularly in DNA replication and the maintenance of genome integrity. The roles of the nucleosome in regulating gene transcription, and how histone-histone interactions function in shaping the chromatin template. The roles of the histones in determining the structure and morphogenesis of the centromere of the chromosome. The roles of the "SNF/SWI" complex in remodeling chromatin for transcription, and its interaction with the adenovirus E1A oncoprotein.


    Selected Publications
  • Bird, A.W, Yu, D.Y., Pray-Grant, M.G., Qui, Q., Harmon, K.E., Megee, P.C.,Grant, P., Smith, M.M., and Christman, M.F. Histone H4 tail acetylation by Esa1p is required for DNA double strand break repair. Nature 419 411-415 (2002).
  • Glowczewski, L., P. Yang, T. Kalashnikova, M.S. Santisteban, and M.M. Smith. Histone-histone interactions and centromere function. Mol. Cell. Biol. 20 5700-5711 (2000).
  • Hsu, J.-Y., Z.-W. Sun, X. Li, M. Reuben, K. Tatchell, D.K. Bishop, J.M. Grushcow, C.J. Brame, J.A. Caldwell, D.F. Hunt, R. Lin, M.M. Smith, and C.D. Allis. Mitotic phosphorylation of histone H3 is governed by Ipl1/aurora kinase and Glc7/PP1 phosphatase in budding yeast and nematodes. Cell 102 279-291 (2000).
  • Santisteban, M.S., Kalashnikova, T., and Smith, M.M. Histone H2A.Z Regulates Transcription and Is Partially Redundant with Nucleosome Remodeling Complexes Cell 103 411-422 (2000).
  • PubMed Listings for this Faculty Member

  • Intranet Profile
    [To add/update Intranet profile information, read these instructions.]

    Contact Information
      Office Address: PO Box 800734, Jordan Hall, 7223, 
      Office Phone: +1 434-924-2669, +1 434-924-8163
      Fax Phone: +1 434-982-1071
      Home Phone: +1 434-974-6156

    Other Websites for this mentor:
    http://www.people.virginia.edu/%7Emms7r/

    (Find Out How to Update Your Faculty Profile)