TY - JOUR
T1 - MCAF mediates MBD1-dependent transcriptional repression
AU - Fujita, Naoyuki
AU - Watanabe, Sugiko
AU - Ichimura, Takaya
AU - Ohkuma, Yoshiaki
AU - Chiba, Tsutomu
AU - Saya, Hideyuki
AU - Nakao, Mitsuyoshi
PY - 2003/4
Y1 - 2003/4
N2 - DNA methylation is involved in a variety of genome functions, including gene control and chromatin dynamics. MBD1 is a transcriptional regulator through the cooperation of a methyl-CpG binding domain, cysteine-rich CXXC domains, and a transcriptional repression domain. A yeast two-hybrid screen was performed to investigate the role of MBD1 in methylation-based transcriptional repression. We report a mediator, MBD1-containing chromatin-associated factor (MCAF), that interacts with the transcriptional repression domain of MBD1. MCAF harbors two conserved domains that allow it to interact with MBD1 and enhancer-like transactivator Sp1. MCAF possesses a coactivator-like activity, and it seems to facilitate Sp1-mediated transcription. In contrast, the MBD1-MCAF complex blocks transcription through affecting Sp1 on methylated promoter regions. These data provide a mechanistic basis for direct inhibition of gene expression via methylation-dependent and histone deacetylation-resistant processes.
AB - DNA methylation is involved in a variety of genome functions, including gene control and chromatin dynamics. MBD1 is a transcriptional regulator through the cooperation of a methyl-CpG binding domain, cysteine-rich CXXC domains, and a transcriptional repression domain. A yeast two-hybrid screen was performed to investigate the role of MBD1 in methylation-based transcriptional repression. We report a mediator, MBD1-containing chromatin-associated factor (MCAF), that interacts with the transcriptional repression domain of MBD1. MCAF harbors two conserved domains that allow it to interact with MBD1 and enhancer-like transactivator Sp1. MCAF possesses a coactivator-like activity, and it seems to facilitate Sp1-mediated transcription. In contrast, the MBD1-MCAF complex blocks transcription through affecting Sp1 on methylated promoter regions. These data provide a mechanistic basis for direct inhibition of gene expression via methylation-dependent and histone deacetylation-resistant processes.
UR - http://www.scopus.com/inward/record.url?scp=0037385288&partnerID=8YFLogxK
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U2 - 10.1128/MCB.23.8.2834-2843.2003
DO - 10.1128/MCB.23.8.2834-2843.2003
M3 - Article
C2 - 12665582
AN - SCOPUS:0037385288
SN - 0270-7306
VL - 23
SP - 2834
EP - 2843
JO - Molecular and cellular biology
JF - Molecular and cellular biology
IS - 8
ER -