Abstract
Parafibromin, the product of the HRPT2 (hyperparathyroidism-jaw tumor syndrome 2) tumor suppressor gene, is the human homologue of yeast Cdc73, part of the yeast RNA polymerase II/Paf1 complex known to be important for histone modification and connections to posttranscriptional events. By purifying cellular parafibromin and characterizing its associated proteins, we have identified a human counterpart to the yeast Paf1 complex including homologs of Leo1, Paf1, and Ctr9. Like the yeast complex, the parafibromin complex associates with the nonphosphorylated and Ser2 and Ser5 phosphorylated forms of the RNA polymerase II large subunit. Immunofluorescence experiments show that parafibromin is a nuclear protein. In addition, cotransfection data suggest that parafibromin can interact with a histone methyltransferase complex that methylates histone H3 on lysine 4. Some mutant forms of parafibromin lack association with hPaf1 complex members and with the histone methyltransferase complex, suggesting that disruption of these complexes may correlate with the oncogenic process.
ACKNOWLEDGMENTS
We thank E. McIntush at Bethyl Laboratories for antibody design, E. Kort and E. Hudson for immunofluorescence assay assistance, and J. W. Lee for the ASC-2 antibody. We are grateful to the Taplin Biological Institute for mass spectrometry analysis and Bethyl Laboratories for preparation of polyclonal antibodies. We also thank J. Jaehning and G. David for critical comments on the manuscript and helpful discussions.
This work was supported by a gift from Raymond and Beverly Sackler.