Posttranscriptional regulation of chicken ccn2 gene expression by nucleophosmin/B23 during chondrocyte differentiation

被引:24
作者
Mukudai, Yoshiki [2 ]
Kubota, Satoshi [1 ]
Kawaki, Harumi [1 ]
Kondo, Seiji [1 ]
Eguchi, Takanori [1 ]
Sumiyoshi, Kumi [1 ]
Ohgawara, Toshihiro [1 ,3 ]
Shimo, Tsuyoshi [3 ]
Takigawa, Masaharu [1 ,2 ]
机构
[1] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Biochem & Mol Dent, Okayama 7008525, Japan
[2] Okayama Univ, Sch Dent, Biodental Res Ctr, Okayama 7008525, Japan
[3] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Oral & Maxillofacial Surg & Biopathol Sci, Okayama 7008525, Japan
关键词
D O I
10.1128/MCB.00495-08
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
CCN2/CTGF is a multifunctional factor that plays a crucial role in the growth and differentiation of chondrocytes. The chicken ccn2 gene is regulated not only at the transcriptional level but also by the interaction between a posttranscriptional element in the 3' untranslated region (3'-UTR) and a cofactor. In the present study, we identified a nucleophosmin (NPM) (also called B23) as this cofactor. Binding of NPM to the element was confirmed, and subsequent analysis revealed a significant correlation between the decrease in cytosolic NPM and the increased stability of the ccn2 mRNA during chondrocyte differentiation in vivo. Furthermore, recombinant chicken NPM enhanced the degradation of chimeric RNAs containing the posttranscriptional cis elements in a chicken embryonic fibroblast extract in vitro. It is noteworthy that the RNA destabilization effect by NPM was far more prominent in the cytosolic extract of chondrocytes than in that of fibroblasts, representing a chondrocyte-specific action of NPM. Stimulation by growth factors to promote differentiation changed the subcellular distribution of NPM in chondrocytes, which followed the expected patterns from the resultant change in the ccn2 mRNA stability. Therefore, the present study reveals a novel aspect of NPM as a key player in the posttranscriptional regulation of ccn2 mRNA during the differentiation of chondrocytes.
引用
收藏
页码:6134 / 6147
页数:14
相关论文
共 79 条
[21]   THE RIBONUCLEASE-ACTIVITY OF NUCLEOLAR PROTEIN B23 [J].
HERRERA, JE ;
SAVKUR, R ;
OLSON, MOJ .
NUCLEIC ACIDS RESEARCH, 1995, 23 (19) :3974-3979
[22]   Mapping the functional domains of nucleolar protein B23 [J].
Hingorani, K ;
Szebeni, A ;
Olson, MOJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (32) :24451-24457
[23]   REGULATION OF CONNECTIVE-TISSUE GROWTH-FACTOR GENE-EXPRESSION IN HUMAN SKIN FIBROBLASTS AND DURING WOUND REPAIR [J].
IGARASHI, A ;
OKOCHI, H ;
BRADHAM, DM ;
GROTENDORST, GR .
MOLECULAR BIOLOGY OF THE CELL, 1993, 4 (06) :637-645
[24]  
INOUYE CJ, 1994, J BIOL CHEM, V269, P6506
[25]   PROVIRAL REARRANGEMENTS AND OVEREXPRESSION OF A NEW CELLULAR GENE (NOV) IN MYELOBLASTOSIS-ASSOCIATED VIRUS TYPE-1-INDUCED NEPHROBLASTOMAS [J].
JOLIOT, V ;
MARTINERIE, C ;
DAMBRINE, G ;
PLASSIART, G ;
BRISAC, M ;
CROCHET, J ;
PERBAL, B .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (01) :10-21
[26]   TERMINAL DIFFERENTIATION AND CALCIFICATION IN RABBIT CHONDROCYTE CULTURES GROWN IN CENTRIFUGE TUBES - REGULATION BY TRANSFORMING GROWTH FACTOR-BETA AND SERUM FACTORS [J].
KATO, Y ;
IWAMOTO, M ;
KOIKE, T ;
SUZUKI, F ;
TAKANO, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (24) :9552-9556
[27]   Platelet derived growth factor stimulates chondrocyte proliferation but prevents endochondral maturation [J].
Kieswetter, K ;
Schwartz, Z ;
Alderete, M ;
Dean, DD ;
Boyan, BD .
ENDOCRINE, 1997, 6 (03) :257-264
[28]   GROWTH-REGULATION IN SCLERODERMA FIBROBLASTS - INCREASED RESPONSE TO TRANSFORMING GROWTH-FACTOR-BETA-1 [J].
KIKUCHI, K ;
KADONO, T ;
IHN, H ;
SATO, S ;
IGARASHI, A ;
NAKAGAWA, H ;
TAMAKI, K ;
TAKEHARA, K .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1995, 105 (01) :128-132
[29]   Cyr61 and Fisp12 are both ECM-associated signaling molecules: Activities, metabolism, and localization during development [J].
Kireeva, ML ;
Latinkic, BV ;
Kolesnikova, TV ;
Chen, CC ;
Yang, GP ;
Abler, AS ;
Lau, LF .
EXPERIMENTAL CELL RESEARCH, 1997, 233 (01) :63-77
[30]   Characterization of a mouse ctgf 3′-UTR segment that mediates repressive regulation of gene expression [J].
Kondo, S ;
Kubota, S ;
Eguchi, T ;
Hattori, T ;
Nakanishi, T ;
Sugahara, T ;
Takigawa, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 278 (01) :119-124