Opposing functions of ZEB proteins in the regulation of the TGFβ/BMP signaling pathway

被引:261
作者
Postigo, AA [1 ]
机构
[1] Washington Univ, Sch Med, Dept Internal Med, Div Mol Oncol, St Louis, MO 63110 USA
关键词
Smad proteins; TGF beta; BMP signaling; transcriptional regulation; ZEB-1; delta EF1; ZEB-2; SIP1;
D O I
10.1093/emboj/cdg225
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
Binding of TGFbeta/BMP factors to their receptors leads to translocation of Smad proteins to the nucleus where they activate transcription of target genes. The two-handed zinc finger proteins encoded by Zfhx1a and Zfhx1b, ZEB-1/deltaEF1 and ZEB-2/SIP1, respectively, regulate gene expression and differentiation programs in a number of tissues. Here I demonstrate that ZEB proteins are also crucial regulators of TGFbeta/BMP signaling with opposing effects on this pathway. Both ZEB proteins bind to Smads, but while ZEB-1/deltaEF1 synergizes with Smad proteins to activate transcription, promote osteoblastic differentiation and induce cell growth arrest, the highly related ZEB-2/SIP1 protein has the opposite effect. Finally, the ability of TGFbeta to mediate transcription of TGFbeta-dependent genes and induce growth arrest depends on the presence of endogenous ZEB-1/deltaEF1 protein.
引用
收藏
页码:2443 / 2452
页数:10
相关论文
共 67 条
[1]
Smads as transcriptional co-modulators [J].
Attisano, L ;
Wrana, JL .
CURRENT OPINION IN CELL BIOLOGY, 2000, 12 (02) :235-243
[2]
Positive and negative regulation of myogenic differentiation of C2C12 cells by isoforms of the multiple homeodomain zinc finger transcription factor ATBF1 [J].
Berry, FB ;
Miura, Y ;
Mihara, K ;
Kaspar, P ;
Sakata, N ;
Hashimoto-Tamaoki, T ;
Tamaoki, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (27) :25057-25065
[3]
Negative regulation of CD4 expression in T cells by the transcriptional repressor ZEB [J].
Brabletz, T ;
Jung, A ;
Hlubek, F ;
Löhberg, C ;
Meiler, J ;
Suchy, U ;
Kirchner, T .
INTERNATIONAL IMMUNOLOGY, 1999, 11 (10) :1701-1708
[4]
Broihier HT, 1998, DEVELOPMENT, V125, P655
[5]
Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease [J].
Cacheux, V ;
Dastot-Le Moal, F ;
Kääriäinen, H ;
Bondurand, N ;
Rintala, R ;
Boissier, B ;
Wilson, M ;
Mowat, D ;
Goossens, M .
HUMAN MOLECULAR GENETICS, 2001, 10 (14) :1503-1510
[6]
Chamberlain EM, 1999, MOL CELL BIOL, V19, P3600
[7]
Smad4 and FAST-1 in the assembly of activin-responsive factor [J].
Chen, X ;
Weisberg, E ;
Fridmacher, V ;
Watanabe, M ;
Naco, G ;
Whitman, M .
NATURE, 1997, 389 (6646) :85-89
[8]
CtBP, an unconventional transcriptional corepressor in development and oncogenesis [J].
Chinnadurai, G .
MOLECULAR CELL, 2002, 9 (02) :213-224
[9]
Christian JL, 1999, BIOESSAYS, V21, P382, DOI 10.1002/(SICI)1521-1878(199905)21:5<382::AID-BIES5>3.0.CO
[10]
2-V