Repression of p15(INK4b) expression by Myc through association with Miz-1

Citation
P. Staller et al., Repression of p15(INK4b) expression by Myc through association with Miz-1, NAT CELL BI, 3(4), 2001, pp. 392-399
Citations number
47
Categorie Soggetti
Cell & Developmental Biology
Journal title
NATURE CELL BIOLOGY
ISSN journal
14657392 → ACNP
Volume
3
Issue
4
Year of publication
2001
Pages
392 - 399
Database
ISI
SICI code
1465-7392(200104)3:4<392:ROPEBM>2.0.ZU;2-9
Abstract
Deregulated expression of c-myc can induce cell proliferation in establishe d cell lines and in primary mouse embryonic fibroblasts (MEFs), through a c ombination of both transcriptional activation and repression by Myc. Here w e show that a Myc-associated transcription factor, Miz-1, arrests cells in G1 phase and inhibits cyclin D-associated kinase activity. Miz-1 upregulate s expression of the cyclin-dependent kinases (CDK) inhibitor p15(INK4b) by binding to the initiator element of the p15(INK4b) promoter. Myc and Max fo rm a complex with Miz-1 at the p15 initiator and inhibit transcriptional ac tivation by Miz-1. Expression of Myc in primary cells inhibits the accumula tion of p15(INK4b) that is associated with cellular senescence; conversely deletion of c-myc in an established cell line activates p15(INK4b) expressi on. Alleles of c-myc that are unable to bind to Miz-1 fail to inhibit accum ulation of p15(INK4b) messenger RNA in primary cells and are, as a conseque nce, deficient in immortalization.