NSPcl, a mainly nuclear localized protein of novel PcG family members, has a transcription repression activity related to its PKC phosphorylation site at S183

被引:25
作者
Gong, YH
Wang, X
Liu, J
Shi, L
Yin, B
Peng, XZ [1 ]
Qiang, BQ
Yuan, JG
机构
[1] Chinese Acad Med Sci, Inst Basic Med Sci, Natl Lab Med Mol Biol, Beijing 100005, Peoples R China
[2] Peking Union Med Coll, Natl Human Genome Ctr, Beijing 100005, Peoples R China
基金
中国国家自然科学基金;
关键词
PcG; RING finger; transcriptional repression; PKC phosphorylation;
D O I
10.1016/j.febslet.2004.11.056
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Nervous system polycomb 1 (NSPc1) shares high homology with vertebrate PcG proteins Mel-18 and Bmi-1. The mRNA of NSPc1 is highly expressed in the developmental nervous system [Mech. Dev. 102 (2001) 219-222]. However, the functional characterization of NSPc1 protein is not clear. In the present study, using Western blotting technique, we aimed to describe the distributions of NSPc1 protein in rat tissues and cell lines. The subcellular localization of NSPc1 was examined in HeLa and SH-SY5Ycell lines, and its transcriptional repression activity was examined in COS-7 cell line. We found that the NSPc1 protein was localized mainly in the nucleus. NSPc1 remarkably repressed the transcription. Most interestingly, both the C-terminal of NSPc1 and two phosphorylation sites in the C-terminal, especially the PKC phosphorylation site at S183, were important in mediating transcription repression. Taken together, results front our study suggest that NSPc1, as a typical PcG family member, has powerful transcriptional repression ability, which may be related to the PKC signaling pathway. (C) 2004 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:115 / 121
页数:7
相关论文
共 23 条
[1]
Akasaka T, 2001, DEVELOPMENT, V128, P1587
[2]
MBLR, a new RING finger protein resembling mammalian Polycomb gene products, is regulated by cell cycle-dependent phosphorylation [J].
Akasaka, T ;
Takahashi, N ;
Suzuki, M ;
Koseki, H ;
Bodmer, R ;
Koga, H .
GENES TO CELLS, 2002, 7 (08) :835-850
[3]
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]
DROSOPHILA GENES POSTERIOR SEX COMBS AND SUPPRESSOR 2 OF ZESTE ENCODE PROTEINS WITH HOMOLOGY TO THE MURINE BMI-1 ONCOGENE [J].
BRUNK, BP ;
MARTIN, EC ;
ADLER, PN .
NATURE, 1991, 353 (6342) :351-353
[5]
TRANSCRIPTIONAL REPRESSION BY DROSOPHILA AND MAMMALIAN POLYCOMB GROUP PROTEINS IN TRANSFECTED MAMMALIAN-CELLS [J].
BUNKER, CA ;
KINGSTON, RE .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (03) :1721-1732
[6]
Cohen KJ, 1996, MOL CELL BIOL, V16, P5527
[7]
A functional YY1 binding site is necessary and sufficient to activate Surf-1 promoter activity in response to serum growth factors [J].
Cole, EG ;
Gaston, K .
NUCLEIC ACIDS RESEARCH, 1997, 25 (18) :3705-3711
[8]
ACCURATE TRANSCRIPTION INITIATION BY RNA POLYMERASE-II IN A SOLUBLE EXTRACT FROM ISOLATED MAMMALIAN NUCLEI [J].
DIGNAM, JD ;
LEBOVITZ, RM ;
ROEDER, RG .
NUCLEIC ACIDS RESEARCH, 1983, 11 (05) :1475-1489
[9]
Ubiquitination: RING for destruction? [J].
Freemont, PS .
CURRENT BIOLOGY, 2000, 10 (02) :R84-R87
[10]
Dimerization of the Polycomb-group protein Mel-18 is regulated by PKC phosphorylation [J].
Fujisaki, S ;
Ninomiya, Y ;
Ishihara, H ;
Miyazaki, M ;
Kanno, R ;
Asahara, T ;
Kanno, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 300 (01) :135-140