Professor, Biological Chemistry
B.S, M.S., Washington State University
Ph.D., University of California, Berkeley
Postdoctoral, Roche Institute of Molecular Biology
Our laboratory is interested in the regulation of transcription in mammalian cells. The differential regulation of each gene is essential for the appropriate growth and development of the organism. This task is accomplished through the coordinated function of multiple transcription regulatory proteins at each promoter. The selective regulation of gene expression requires that transcription factors are able to interact with each other in many different combinations, yet that their interactions are specific such that they can only occur at particular regulatory elements or in response to specific stimuli. Thus, the key to understanding transcription regulatory specificity is discovery of the mechanisms that control transcription factor interactions.
We focus on investigation of networks of protein interactions and studies of the architectures of nucleoprotein complexes. We have developed many new methods for the study of these areas that enable visualization of protein interactions in living cells and analysis of the structural organization and dynamics of transcription factor complexes in vitro. These approaches provide unique opportunities for us to investigate molecular processes in a physiological context. The goal of our studies is to understand how different combinations of proteins cooperate to produce distinct functional outcomes in different cell types and in response to different extracellular stimuli. In these studies, we focus on the functions of proto-oncogene transcription factors related to c-fos, c-jun, c-maf and c-myc in the regulation of developmental and immunomodulatory genes.
Our previous studies of transcription factor interactions have produced several discoveries that have fundamentally altered our understanding of transcription regulatory mechanisms. David Leonard developed the gel based fluorescence resonance energy transfer (gelFRET) assay, and found that Fos-Jun heterodimers bound to AP-1 sites in a preferred orientation. Vladimir Ramirez-Carrozzi found that electrostatic interactions with sequences flanking the AP-1 site controlled the orientation of Fos-Jun binding and determined the cooperativity of DNA binding and transcription activation with the nuclear factor of activated T cells (NFAT1). Chang-Deng Hu developed the bimolecular fluorescence complementation (BiFC) assay and demonstrated that Fos-Jun heterodimers form more efficiently than Fos-ATF2 or Jun-ATF2 heterodimers when all three proteins are expressed in the same cell. Asya Grinberg found that Myc and Mad family proteins compete with different efficiencies for dimerization with Max in cells, and that they can all interact with Smad family transcription factors. Nirmala Rajaram discovered that Maf and Sox family proteins cooperate to regulate crystallin gene expression, and that a mutation in Maf that causes cataract alters the subnuclear localization and transcriptional activity of the complex. Present laboratory members are continuing to make new discoveries that add to our understanding of transcription regulatory mechanisms.
Vincenz, C. and Kerppola, TK. Different polycomb group CBX family proteins associate with distinct regions of chromatin using non-homologous protein sequences. Proc. Natl. Acad. Sci. U.S.A., 105: 16572-16577 (2008) [DOI] [PDF]
Ikeda, H and Kerppola, TK. Lysosomal localization of ubiquitinated Jun requires multiple determinants in a lysine-27 linked polyubiquitin conjugate. Molecular Biology of the Cell, 19: 4588-4601 (2008) [DOI] [PDF]
Ren, X, Vincenz, C and Kerppola TK. Changes in the distributions and dynamics of polycomb repressive complexes during embryonic stem cell differentiation. Molecular and Cellular Biology 28: 2884-2895 (2008) [DOI] [PDF]
Fang, D. and Kerppola, T. K. Ubiquitin-mediated fluorescence complementation reveals that Jun ubiquitinated by Itch/AIP4 is localized to lysosomes. Proc. Natl. Acad. Sci. U.S.A. 101: 14782-14787 (2004) [Abstract] [Full text] [PDF]
Rajaram, N. and Kerppola, T. K. Synergistic transcription activation by Maf and Sox, and their subnuclear localization are disrupted by a mutation in Maf that causes cataract. Molecular and Cellular Biology 24: 5694-5709 (2004) [Abstract] [Full text] [PDF]
Grinberg, A. V., Hu, C-. D. and Kerppola, T. K. Visualization of Myc/Max/Mad family dimers and the competition for dimerization in living cells. Molecular and Cellular Biology 24: 4294â€“4308 (2004) [Abstract] [Full text] [PDF]
Hu, C-.D. and Kerppola, T.K. Simultaneous visualization of multiple protein interactions in living cells using multicolor fluorescence complementation analysis. Nature Biotechnology 21: 539-545 (2003) [Abstract] [Full text] [PDF]
Ramirez-Carrozzi, V. R. and Kerppola, T. K. Asymmetric recognition of nonconsensus AP-1 sites by Fos-Jun and Jun-Jun influences transcriptional cooperativity with NFAT1. Molecular and Cellular Biology. 23: 1737-1749 (2003) [Abstract] [Full text] [PDF]
Hu, C-.D., Chinenov, Y. and Kerppola, T.K. Visualization of interactions among bZIP and Rel family proteins in living cells using bimolecular fluorescence complementation. Molecular Cell 9: 789-798 (2002) [Abstract] [Full text] [PDF]