Open AccessGfi-1 represses CDKN2B encoding p15 INK4B through interaction with Miz-1
Author(s) -
Suchitra Basu,
Qingquan Liu,
Yaling Qiu,
Daiming Fan
Publication year - 2009
Publication title -
proceedings of the national academy of sciences of the united states of america
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0804863106
Subject(s) - repressor , promoter , zinc finger , transcription factor , psychological repression , biology , transcription (linguistics) , gene knockdown , gene , carcinogenesis , microbiology and biotechnology , transcriptional regulation , genetics , gene expression , linguistics , philosophy
Gfi-1 is a nuclear zinc finger (ZF) transcriptional repressor that plays an important role in hematopoiesis and inner ear development, and has been implicated in lymphomagenesis. Gfi-1 represses transcription by directly binding to the consensus DNA sequence in the promoters of its target genes. We report here an alternative mechanism by which Gfi-1 repressesCDKN2B encoding p15INK4B . Gfi-1 does not directly bind toCDKN2B , but interacts with Miz-1 and, via Miz-1, is recruited to the core promoter ofCDKN2B . Miz-1 is a POZ-ZF transcription factor that has been shown to mediate transcriptional repression by c-Myc. Like c-Myc, upon recruitment to theCDKN2B promoter, Gfi-1 represses transcriptional activation ofCDKN2B by Miz-1 and in response to TGFβ. Consistent with its role in repressingCDKN2B transcription, knockdown of Gfi-1 in human leukemic cells or deficiency of Gfi-1 in mouse bone marrow cells results in augmented expression of p15INK4B . Notably, Gfi-1 and c-Myc are both recruited to theCDKN2B core promoter and act in collaboration to repressCDKN2B . Our data reveal a mechanism of transcriptional repression by Gfi-1 and may have important implications for understanding the roles of Gfi-1 in normal development and tumorigenesis.