共 45 条
ORC1 interacts with c-Myc to inhibit E-box-dependent transcription by abrogating c-Myc-SNF5/INI1 interaction
被引:35
作者:
Takayama, M
Taira, T
Tamai, K
Iguchi-Ariga, AMM
Ariga, H
[1
]
机构:
[1] Hokkaido Univ, Grad Sch Pharmaceut Sci, Kita Ku, Sapporo, Hokkaido 060, Japan
[2] Hokkaido Univ, Coll Med Technol, Kita Ku, Sapporo, Hokkaido 060, Japan
[3] MBL Co Ltd, Ina Labs, Ina, Saitama 396, Japan
[4] Japan Sci & Technol Corp, CREST, Kawaguchi, Saitama 3320012, Japan
关键词:
D O I:
10.1046/j.1365-2443.2000.00338.x
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Background: The c-myc oncogene product (c-Myc) is a transcription factor that forms a complex with Max and recognizes the E-box sequence. c-Myc plays key functions in cell proliferation, differentiation and apoptosis. As for its activity towards cell proliferation, it is generally thought that c-Myc transactivates the E-box-containing genes that encode proteins essential to cell-cycle progression. Despite the characterization of candidate genes regulated by c-Myc in culture cells, these have still not been firmly recognized as real target genes for c-Myc. Results: We found that c-Myc directly bound to the N-terminal region of origin recognition complex-1 (ORC1), a region that is responsible for gene silencing, in a state of complex containing other ORC subunits and Max in vivo and in vitro. Furthermore, ORC1 inhibited E-box-dependent transcription activity of c-Myc by competitive binding to the C-terminal region of c-Myc with SNF5, a component of chromatin remodelling complex SNF/Swi1. Conclusions: These results suggest that ORC1 suppresses the transcription activity of c-Myc by its recruitment into an inactive form of chromatin during some stage of the cell cycle.
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页码:481 / 490
页数:10
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