Tsc-22 enhances TGF-ß signaling by associating with Smad4 and induces erythroid cell differentiation

被引:46
作者
Choi, SJ
Moon, JH
Ahn, YW
Ahn, JH
Kim, DU
Han, TH [1 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Dept Mol Cell Biol, SBRI, Suwon 440746, South Korea
[2] Sungkyunkwan Univ, Sch Med, Ctr Mol Med, SBRI, Suwon 440746, South Korea
[3] Catholic Univ Korea, Catholic Hematopoiet Stem Cell Transplantat Ctr, Seoul 150713, South Korea
关键词
tsc-22; TGD-ss; Smad4; K562;
D O I
10.1007/s11010-005-3456-7
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tsc-22 was isolated as a TGF-beta-inducible gene by differential screening of the mouse osteoblastic cell cDNA library [J Biol Chem 267 (1992) 10219]. tsc-22 mRNA is expressed in almost all organs of mice and humans and its expression is induced in a variety of cell lines by many different factors including TGF-beta, phorbol ester, serum, and progestin. tsc-22 encodes a 18-kd protein that contains a leucine zipper motif and a Tsc-box. The leucine zipper motif of the Tsc-22 protein does not have a basic DNA binding motif and when the protein was fused to a heterologous DNA binding domain, it showed various transcription-modulating activities ranging from activation to repression [J Biol Chem 274 (1999) 27439, Biochem Biophys Res Commun 278 (2000) 659]. Although these results suggest that the Tsc-22 protein functions as a transcriptional regulator recruiting various coactivators or repressors, its mechanism is not known. In this study, we examined whether Tsc-22 modulates the TGF-beta-dependant signaling pathway and found that Tsc-22 binds to and modulate the transcriptional activity of Smad3 and Smad4. Its effect on cellular differentiation was also examined.
引用
收藏
页码:23 / 28
页数:6
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