B-cell lymphoma gene 6: Insights into mechanisms of functional regulation
Krupski-Downs, Melissa A.
MetadataShow full item record
BCL6 is a sequence specific transcription repressor required for germinal center (GC) formation. In normal B cells, BCL6 exerts its regulatory role through repression of genes associated with B cell activation, response to DNA damage, cell-cycle regulation and plasma cell differentiation. Deregulated expression of BCL6 is found in many GC-derived Diffuse Large B cell Lymphomas (DLBCLs). Mouse models engineered to recapitulate BCL6 deregulation in DLBCL have confirmed a causative role for BCL6 in the pathogenesis of these tumors. This study examines BCL6 protein functional modulation caused by its interacting partners, post-translational modification and inactivating mutations. First, resulting from the identification of the HAT protein Tip60 as a BCL6 interacting partner, we examined Tip60-dependent acetylation of BCL6. Ultimately no evidence for this was obtained, however our results suggest a potential role for Tip60 in BCL6 protein stabilization in a HAT-independent manner in Type III DLBCLs. Next we studied BCL6 post-translational modification by the small ubiquitin-like modifier, SUMO. BCL6 contains a number of putative sumoylation sites. Using in vitro and in vivo sumoylation assays, we were able to demonstrate that BCL6 can, in fact, be sumoylated and that BCL6 sumoylation appears to involve multiple substrate lysine sites. Our last study centered on the identification of novel BCL6 coding region mutations. Lymphoma-associated BCL6 deregulation is believed to occur only at the transcriptional level so that lymphoma B cells still express a wild type BCL6 protein. Here we report the identification and characterization of a novel coding region mutation in the zinc finger domain of BCL6 in a DLBCL cell line. The mutation, C579R, disrupts a cysteine residue required for the structural integrity of the third ZF leading to compromised DNA binding and therefore impaired transcriptional repression capacity. In vivo growth/survival assays demonstrate that B cells over-expressing this mutant have an advantage over their WT expressing counterparts. Our data suggest a tumor suppressive activity of BCL6 which can be targeted by spontaneous mutation during lymphomagenesis. In support of this, we also report in this study, the identification of BCL6 mutations in additional DLBCL cell lines and in primary samples from DLBCL patients.