p67 isoform of mouse disabled 2 protein acts as a transcriptional activator during the differentiation of F9 cells

被引:21
作者
Cho, SY [1 ]
Jeon, JW [1 ]
Lee, SH [1 ]
Park, SS [1 ]
机构
[1] Korea Univ, Grad Sch Biotechnol, Seoul 136701, South Korea
关键词
mDab2 interacting protein; proline-rich domain; retinoic acid; transactivation;
D O I
10.1042/0264-6021:3520645
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
The mouse disabled 2 (mDab2) gene is a mouse homologue of the Drosophila disabled gene and is alternatively spliced to form two isoforms, p96 and p67. Although p96 has been known to regulate the Ras-Sos G-protein signal transduction pathway by interacting with Grb2, little is known about the biological function of p67, Recent studies have shown that the expression of mDab2 is markedly up-regulated during the retinoic acid (RA)-induced differentiation of F9 cells, suggesting another role for mDab2 in cell differentiation [Cho, Lee and Park (1999) Mol. Cells 9, 179-184), In the present study, we first elucidated the biological function of p67 isoform of mDab2 and identified its binding partner. Unlike p96, p67 largely resides in RA-treated F9 cell nuclei. In this system, p67 interacts with mouse androgen-receptor interacting protein 3, termed the mDab2 interacting protein, which acts as a transcriptional co-regulator. By using a fusion protein with a heterologous DNA-binding domain (GAL4), we showed that p67 had an intrinsic transcriptional activation function. These results suggest that mDab2 p67 may function as a transcriptional co-factor for certain complexes of transcriptional regulatory elements involved in the-RA-induced differentiation of F9 cells.
引用
收藏
页码:645 / 650
页数:6
相关论文
共 27 条
[1]   Disabled-2 inactivation is an early step in ovarian tumorigenicity [J].
Fazili, Z ;
Sun, WP ;
Mittelstaedt, S ;
Cohen, C ;
Xu, XX .
ONCOGENE, 1999, 18 (20) :3104-3113
[2]   MULTIPLE GENES ENCODE NUCLEAR FACTOR-1-LIKE PROTEINS THAT BIND TO THE PROMOTER FOR 3-HYDROXY-3-METHYLGLUTARYL-COENZYME-A REDUCTASE [J].
GIL, G ;
SMITH, JR ;
GOLDSTEIN, JL ;
SLAUGHTER, CA ;
ORTH, K ;
BROWN, MS ;
OSBORNE, TF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (23) :8963-8967
[3]  
Gorman C., 1985, DNA CLONING PRACTICA, V1, P143
[4]   RECOMBINANT GENOMES WHICH EXPRESS CHLORAMPHENICOL ACETYLTRANSFERASE IN MAMMALIAN-CELLS [J].
GORMAN, CM ;
MOFFAT, LF ;
HOWARD, BH .
MOLECULAR AND CELLULAR BIOLOGY, 1982, 2 (09) :1044-1051
[5]   THE CHICKEN PROGESTERONE-RECEPTOR - SEQUENCE, EXPRESSION AND FUNCTIONAL-ANALYSIS [J].
GRONEMEYER, H ;
TURCOTTE, B ;
QUIRINSTRICKER, C ;
BOCQUEL, MT ;
MEYER, ME ;
KROZOWSKI, Z ;
JELTSCH, JM ;
LEROUGE, T ;
GARNIER, JM ;
CHAMBON, P .
EMBO JOURNAL, 1987, 6 (13) :3985-3994
[6]   EUKARYOTIC PROTEINS EXPRESSED IN ESCHERICHIA-COLI - AN IMPROVED THROMBIN CLEAVAGE AND PURIFICATION PROCEDURE OF FUSION PROTEINS WITH GLUTATHIONE-S-TRANSFERASE [J].
GUAN, KL ;
DIXON, JE .
ANALYTICAL BIOCHEMISTRY, 1991, 192 (02) :262-267
[7]   CDI1, A HUMAN G1-PHASE AND S-PHASE PROTEIN PHOSPHATASE THAT ASSOCIATES WITH CDK2 [J].
GYURIS, J ;
GOLEMIS, E ;
CHERTKOV, H ;
BRENT, R .
CELL, 1993, 75 (04) :791-803
[8]   CELL-INTERACTIONS MODULATE EMBRYONAL CARCINOMA CELL-DIFFERENTIATION INTO PARIETAL OR VISCERAL ENDODERM [J].
HOGAN, BLM ;
TAYLOR, A ;
ADAMSON, E .
NATURE, 1981, 291 (5812) :235-237
[9]   Mouse disabled (mDab1): A Src binding protein implicated in neuronal development [J].
Howell, BW ;
Gertler, FB ;
Cooper, JA .
EMBO JOURNAL, 1997, 16 (01) :121-132
[10]  
Howell BW, 1999, MOL CELL BIOL, V19, P5179