The parafibromin tumor suppressor protein is part of a human Paf1 complex

被引:216
作者
Rozenblatt-Rosen, O
Hughes, CM
Nannepaga, SJ
Shanmugam, KS
Copeland, TD
Guszczynski, T
Resau, JH
Meyerson, M
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[2] Harvard Univ, Dept Pathol, Boston, MA USA
[3] NCI, Canc Res Ctr, Lab Prot Dynam & Signaling, Frederick, MD USA
[4] Van Andel Inst, Mol Microbiol Lab, Grand Rapids, MI USA
关键词
D O I
10.1128/MCB.25.2.612-620.2005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
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收藏
页码:612 / 620
页数:9
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