The ski protein family is required for MeCP2-mediated transcriptional repression

被引:157
作者
Kokura, K
Kaul, SC
Wadhwa, R
Nomura, T
Khan, MM
Shinagawa, T
Yasukawa, T
Colmenares, C
Ishii, S
机构
[1] RIKEN, Tsukuba Inst, Mol Genet Lab, Tsukuba, Ibaraki 3050074, Japan
[2] Japan Sci & Technol Corp, CREST Project, Tsukuba, Ibaraki 3050074, Japan
[3] Agcy Ind Sci & Technol, Natl Inst Biosci & Human Technol, Tsukuba, Ibaraki 3050046, Japan
[4] Chugai Res Inst Mol Med, Niihari, Ibaraki 300101, Japan
[5] Cleveland Clin Fdn, Lerner Res Inst, Dept Canc Biol, Cleveland, OH 44195 USA
关键词
D O I
10.1074/jbc.M105747200
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
DNA methylation is essential for development in the mouse and plays an important role in inactivation of the X chromosome and genomic imprinting. MeCP2 is the founder member of a family of methyl-CpG-binding proteins. MeCP2 directly binds to the co-repressor mSin3, which interacts with class I histone deacetylase, recruiting them to methyl-CpG regions to suppress transcription. Here, we report that MeCP2 directly binds to two co-repressors, c-Ski and N-CoR, in addition to mSin3A, and that the c-Ski, which is encoded by the c-ski proto-onocogene, is required for MeCP2-mediated transcriptional repression. The two regions of c-Ski, including the C-terminal coiled-coil region, interact with the transcriptional repression domain in the center of the MeCP2 molecule. The immunostaining signals for c-Ski and MeCP2 overlap in the nuclear heterochromatin region, suggesting the co-localization of the two proteins. The degree of transcriptional repression mediated by a Gal4-MeCP2 fusion protein was abrogated by overexpression of the putative dominant negative form of c-Ski. Furthermore, injection of antibodies against c-Ski and Sno almost completely abolished the transcriptional repression mediated by the Gal4-MeCP2 fusion protein. These results suggest that the ski gene family is involved in methyl CpG-mediated transcriptional repression.
引用
收藏
页码:34115 / 34121
页数:7
相关论文
共 49 条
[41]   Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex [J].
Nan, XS ;
Ng, HH ;
Johnson, CA ;
Laherty, CD ;
Turner, BM ;
Eisenman, RN ;
Bird, A .
NATURE, 1998, 393 (6683) :386-389
[42]   ISOLATION OF HUMAN CDNA CLONES OF SKI AND THE SKI-RELATED GENE, SNO [J].
NOMURA, N ;
SASAMOTO, S ;
ISHII, S ;
DATE, T ;
MATSUI, M ;
ISHIZAKI, R .
NUCLEIC ACIDS RESEARCH, 1989, 17 (14) :5489-5500
[43]   Ski is a component of the histone deacetylase complex required for transcriptional repression by Mad and thyroid hormone receptor [J].
Nomura, T ;
Khan, MM ;
Kaul, SC ;
Dong, HD ;
Wadhwa, R ;
Colmenares, C ;
Kohno, I ;
Ishii, S .
GENES & DEVELOPMENT, 1999, 13 (04) :412-423
[44]   Solution structure of the methyl-CpG binding domain of human MBD1 in complex with methylated DNA [J].
Ohki, I ;
Shimotake, N ;
Fujita, N ;
Jee, JG ;
Ikegami, T ;
Nakao, M ;
Shirakawa, M .
CELL, 2001, 105 (04) :487-497
[45]   RAPID DETECTION OF OCTAMER BINDING-PROTEINS WITH MINI-EXTRACTS, PREPARED FROM A SMALL NUMBER OF CELLS [J].
SCHREIBER, E ;
MATTHIAS, P ;
MULLER, MM ;
SCHAFFNER, W .
NUCLEIC ACIDS RESEARCH, 1989, 17 (15) :6419-6419
[46]   Interaction of the Ski oncoprotein with Smad3 regulates TGF-β signaling [J].
Sun, Y ;
Liu, XD ;
Eaton, EN ;
Lane, WS ;
Lodish, HF ;
Weinberg, RA .
MOLECULAR CELL, 1999, 4 (04) :499-509
[47]   Viral ski inhibits retinoblastoma protein (Rb)-mediated transcriptional repression in a dominant negative fashion [J].
Tokitou, F ;
Nomura, T ;
Khan, MM ;
Kaul, SC ;
Wadhwa, R ;
Yasukawa, T ;
Kohno, I ;
Ishii, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (08) :4485-4488
[48]   Ski acts as a co-repressor with Smad2 and Smad3 to regulate the response to type β transforming growth factor [J].
Xu, WD ;
Angelis, K ;
Danielpour, D ;
Haddad, MM ;
Bischof, O ;
Campisi, J ;
Stavnezer, E ;
Medrano, EE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (11) :5924-5929
[49]   Histone deacetylases and SAP18, a novel polypeptide, are components of a human Sin3 complex [J].
Zhang, Y ;
Iratni, R ;
ErdjumentBromage, H ;
Tempst, P ;
Reinberg, D .
CELL, 1997, 89 (03) :357-364