Signaling disrupts mSin3A binding to the Mad1-like Sin3-interacting domain of TIEG2, an Sp1-like repressor

被引:48
作者
Ellenrieder, V
Zhang, JS
Kaczynski, J
Urrutia, R [1 ]
机构
[1] Mayo Clin & Mayo Fdn, Gastroenterol Res Unit, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Tumor Biol Program, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
[4] Univ Ulm, Dept Internal Med, D-7900 Ulm, Germany
关键词
EGF; mSin3A; repression; SID; TIEG2;
D O I
10.1093/emboj/21.10.2451
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 Sin3-interacting domain (SID) originally described in Mad proteins is necessary for both transcriptional repression and growth suppression by these transcription factors. We recently reported that a structurally and functionally related Mad1-like SID is also present in five Sp1-like repressor proteins (TIEG1, TIEG2, BTEB1, BTEB3 and BTEB4), demonstrating that SID-mSin3A interactions have a wider functional impact on transcriptional repression. SID-mSin3A interaction is necessary for the anti-proliferative function of Mad, TIEG and BTEB proteins. It remains to be established, however, whether the SID-mSin3A interaction is constitutive or regulated. Here, we describe that the Mad1-like SID domain of the Sp1-like repressor TIEG2 is inhibited by the epidermal growth factor (EGF)-Ras-MEK1-ERK2 signaling pathway, via phosphorylation of four serine/threonine sites adjacent to the SID. This phenomenon disrupts the SID-mSin3A interaction and thereby inhibits TIEG2's repression activity. Thus, these results show for the first time that the repression of a SID-containing protein is regulated by signaling rather than functioning in a constitutive manner, extending our understanding of how the function of SID-containing repressors may be controlled.
引用
收藏
页码:2451 / 2460
页数:10
相关论文
共 26 条
[1]   Mad1 function is regulated through elements within the carboxy terminus [J].
Barrera-Hernandez, G ;
Cultraro, CM ;
Pianetti, S ;
Segal, S .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (12) :4253-4264
[2]   CASEIN KINASE-II INHIBITS THE DNA-BINDING ACTIVITY OF MAX HOMODIMERS BUT NOT MYC MAX HETERODIMERS [J].
BERBERICH, SJ ;
COLE, MD .
GENES & DEVELOPMENT, 1992, 6 (02) :166-176
[3]   Sp1 and kruppel-like factor family of transcription factors in cell growth regulation and cancer [J].
Black, AR ;
Black, JD ;
Azizkhan-Clifford, J .
JOURNAL OF CELLULAR PHYSIOLOGY, 2001, 188 (02) :143-160
[4]  
BOUSSET K, 1993, ONCOGENE, V8, P3211
[5]   Solution structure of the interacting domains of the Mad-Sin3 complex: Implications for recruitment of a chromatin-modifying complex [J].
Brubaker, K ;
Cowley, SM ;
Huang, K ;
Loo, L ;
Yochum, GS ;
Ayer, DE ;
Eisenman, RN ;
Radhakrishnan, I .
CELL, 2000, 103 (04) :655-665
[6]   Groucho/TLE family proteins and transcriptional repression [J].
Chen, GQ ;
Courey, AJ .
GENE, 2000, 249 (1-2) :1-16
[7]   Three conserved transcriptional repressor domains are a defining feature of the TIEG subfamily of Sp1-like zinc finger proteins [J].
Cook, T ;
Gebelein, B ;
Belal, M ;
Mesa, K ;
Urrutia, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (41) :29500-29504
[8]   TIEG proteins join the Smads as TGF-β-regulated transcription factors that control pancreatic cell growth [J].
Cook, T ;
Urrutia, R .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2000, 278 (04) :G513-G521
[9]   Molecular cloning and characterization of TIEG2 reveals a new subfamily of transforming growth factor-β-inducible Sp1-like zinc finger-encoding genes involved in the regulation of cell growth [J].
Cook, T ;
Gebelein, B ;
Mesa, K ;
Mladek, A ;
Urrutia, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (40) :25929-25936
[10]   Regulation of nuclear localization during signaling [J].
Cyert, MS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (24) :20805-20808