TY - JOUR
T1 - Microspherule protein 1, Mi-2β, and RET finger protein associate in the nucleolus and up-regulate ribosomal gene transcription
AU - Shimono, Keiko
AU - Shimono, Yohei
AU - Shimokata, Kaoru
AU - Ishiguro, Naoki
AU - Takahashi, Masahide
PY - 2005/11/25
Y1 - 2005/11/25
N2 - The nucleolus is the site of ribosomal DNA (rDNA) transcription and ribosome production. In exploring the role of nucleolar protein MCRS1 (microspherule protein1)/MSP58 (58-kDa microspherule protein), we found that Mi-2β, a component of a nucleosome remodeling and deacetylase (NuRD) complex, RET finger protein (RFP), and upstream binding factor (UBF) were associated with MCRS1. Yeast two-hybrid assays revealed that MCRS1 bound to the ATPase/helicase region of Mi-2β and the coiled-coil region of RFP. Interestingly, confocal microscopic analyses revealed the co-localization of MCRS1, Mi-2β, RFP, and the rRNA transcription factor UBF in the nucleoli. We also found that MCRS1, Mi-2β, and RFP were associated with rDNA using a chromatin immunoprecipitation assay. Finally, we showed that MCRS1, Mi-2β, and RFP up-regulated transcriptional activity of the rDNA promoter and that ribosomal RNA transcription was repressed when MCRS1, Mi-2β, and RFP expression was reduced using siRNA. These results indicated that Mi-2β and RFP, known to be involved in transcriptional repression in the nucleus, co-localize with MCRS1 in the nucleolus and appear to activate the rRNA transcription.
AB - The nucleolus is the site of ribosomal DNA (rDNA) transcription and ribosome production. In exploring the role of nucleolar protein MCRS1 (microspherule protein1)/MSP58 (58-kDa microspherule protein), we found that Mi-2β, a component of a nucleosome remodeling and deacetylase (NuRD) complex, RET finger protein (RFP), and upstream binding factor (UBF) were associated with MCRS1. Yeast two-hybrid assays revealed that MCRS1 bound to the ATPase/helicase region of Mi-2β and the coiled-coil region of RFP. Interestingly, confocal microscopic analyses revealed the co-localization of MCRS1, Mi-2β, RFP, and the rRNA transcription factor UBF in the nucleoli. We also found that MCRS1, Mi-2β, and RFP were associated with rDNA using a chromatin immunoprecipitation assay. Finally, we showed that MCRS1, Mi-2β, and RFP up-regulated transcriptional activity of the rDNA promoter and that ribosomal RNA transcription was repressed when MCRS1, Mi-2β, and RFP expression was reduced using siRNA. These results indicated that Mi-2β and RFP, known to be involved in transcriptional repression in the nucleus, co-localize with MCRS1 in the nucleolus and appear to activate the rRNA transcription.
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U2 - 10.1074/jbc.M507356200
DO - 10.1074/jbc.M507356200
M3 - Article
C2 - 16186106
AN - SCOPUS:28244475343
SN - 0021-9258
VL - 280
SP - 39436
EP - 39447
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 47
ER -