Yin-yang 1 and glucocorticoid receptor participate in the Stat5-mediated growth hormone response of the serine protease inhibitor 2.1 gene

被引:27
作者
Bergad, PL
Towle, HC
Berry, SA
机构
[1] Univ Minnesota, Dept Pediat, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Biochem Mol Biol & Biophys, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Inst Human Genet, Minneapolis, MN 55455 USA
关键词
D O I
10.1074/jbc.275.11.8114
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
A growth hormone-inducible nuclear factor complex (GHINF), affinity-purified using the growth hormone response element (GHRE) from the promoter of rat serine protease inhibitor 2.1, was found to contain Stat5a and -5b, as well as additional components. The ubiquitous transcription factor yin-yang 1 (YY1) is present in GHINF.An antibody to YY1 inhibited the formation of the GHINF GHRE complex in an electrophoretic mobility shift assay. Furthermore, Stat5 was co-immunoprecipitated from rat hepatic nuclear extracts with antibodies to YY1. An examination of the GHRE shows that, in addition to two gamma-activated sites, it contains a putative YY1 binding site between the two gamma-activated sites, overlapping them both. Mutation of this putative YY1 site results in a decrease of GHINF GHRE complex formation in an electrophoretic mobility shift assay and a corresponding decrease in growth hormone (GH) response in functional assays. The glucocorticoid receptor was also present in GHINF, and StatB co-immunoprecipitates with glucocorticoid receptor in hepatic nuclear extracts from rats treated with GH, GH activation of serine protease inhibitor 2.1 requires the unique sequence of the GHRE encompassing the recognition sites of several transcription factors, and the interaction of these factors enhances the assembly of the transcription complex.
引用
收藏
页码:8114 / 8120
页数:7
相关论文
共 47 条
[1]   Characterization of the transcriptional regulator YY1 - The bipartite transactivation domain is independent of interaction with the TATA box-binding protein, transcription factor IIB, TAF(II)55, or cAMP-responsive element-binding protein (CBP)-binding protein [J].
Austen, M ;
Luscher, B ;
LuscherFirzlaff, JM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (03) :1709-1717
[2]  
BASU A, 1993, J BIOL CHEM, V268, P4188
[3]   CHARACTERIZATION OF HUCRBP (YY1, NF-E1, DELTA) - A TRANSCRIPTION FACTOR THAT BINDS THE REGULATORY REGIONS OF MANY VIRAL AND CELLULAR GENES [J].
BECKER, KG ;
JEDLICKA, P ;
TEMPLETON, NS ;
LIOTTA, L ;
OZATO, K .
GENE, 1994, 150 (02) :259-266
[4]   GROWTH-HORMONE INDUCTION OF HEPATIC SERINE-PROTEASE INHIBITOR-2.1 TRANSCRIPTION IS MEDIATED BY A STAT5-RELATED FACTOR-BINDING SYNERGISTICALLY TO 2 GAMMA-ACTIVATED SITES [J].
BERGAD, PL ;
SHIH, HM ;
TOWLE, HC ;
SCHWARZENBERG, SJ ;
BERRY, SA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (42) :24903-24910
[5]   ONTOGENY OF GROWTH-HORMONE (GH)-RESPONSIVE HEPATIC GENE-PRODUCTS - LACK OF CORRELATION WITH HEPATIC GH RECEPTOR CONTENT [J].
BERRY, SA ;
MANTHEI, RD ;
SEELIG, S .
ENDOCRINOLOGY, 1986, 119 (05) :2290-2296
[6]   BINDING OF A GROWTH HORMONE-INDUCIBLE NUCLEAR FACTOR IS MEDIATED BY TYROSINE PHOSPHORYLATION [J].
BERRY, SA ;
BERGAD, PL ;
WHALEY, CD ;
TOWLE, HC .
MOLECULAR ENDOCRINOLOGY, 1994, 8 (12) :1714-1719
[7]   ACTIVATION OF ACUTE-PHASE RESPONSE FACTOR (APRF)/STAT3 TRANSCRIPTION FACTOR BY GROWTH-HORMONE [J].
CAMPBELL, GS ;
MEYER, DJ ;
RAZ, R ;
LEVY, DE ;
SCHWARTZ, J ;
CARTERSU, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (08) :3974-3979
[8]   Characterization of Stat5a and Stat5b homodimers and heterodimers and their association with the glucocortiocoid receptor in mammary cells [J].
Cella, N ;
Groner, B ;
Hynes, NE .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (04) :1783-1792
[9]   STATs and gene regulation [J].
Darnell, JE .
SCIENCE, 1997, 277 (5332) :1630-1635
[10]   GROWTH-HORMONE AND ERYTHROPOIETIN DIFFERENTIALLY ACTIVATE DNA-BINDING PROTEINS BY TYROSINE PHOSPHORYLATION [J].
FINBLOOM, DS ;
PETRICOIN, EF ;
HACKETT, RH ;
DAVID, M ;
FELDMAN, GM ;
IGARASHI, K ;
FIBACH, E ;
WEBER, MJ ;
THORNER, MO ;
SILVA, CM ;
LARNER, AC .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (03) :2113-2118