Identification of a Novel Role of ZMIZ2 Protein in Regulating the Activity of the Wnt/β-Catenin Signaling Pathway

被引:20
|
作者
Lee, Suk Hyung
Zhu, Chunfang
Peng, Yue
Johnson, Daniel T.
Lehmann, Lynn
Sun, Zijie [1 ,2 ]
机构
[1] Stanford Univ, Sch Med, Dept Urol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
关键词
-Catenin; Cell Signaling; Protein-Protein Interactions; Transcription Regulation; Wnt Signaling; PIAS-like Proteins; Wnt Ligand; ZMIZ2; PIAS-LIKE PROTEIN; RECEPTOR-MEDIATED TRANSCRIPTION; PROSTATE-CANCER CELLS; P53; TUMOR-SUPPRESSOR; BETA-CATENIN; ANDROGEN RECEPTOR; COLON-CARCINOMA; WNT; COMPLEX; EXPRESSION;
D O I
10.1074/jbc.M113.529727
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
Background: ZMIZ2 is a transcriptional coactivator, but its biological role has not been fully investigated. Results: We demonstrate a promotional role of ZMIZ2 in -catenin-mediated transcription and cell growth using a variety of biologically relevant in vitro and in vivo approaches. Conclusion: ZMIZ2 is a coactivator of the Wnt/-catenin signaling pathway. Significance: This study explores a novel mechanism for PIAS-like proteins in regulating Wnt signaling pathways. ZMIZ2, also named ZIMP7, is a protein inhibitor of activated STAT (PIAS)-like protein and a transcriptional coactivator. In this study, we investigated the interaction between ZMIZ2 and -catenin, a key regulator of the Wnt signaling pathway. We demonstrated that the expression of exogenous ZMIZ2 augments TCF (T cell factor) and -catenin-mediated transcription. In contrast, shRNA knockdown of ZMIZ2 expression specifically represses the enhancement of TCF/-catenin-mediated transcription by ZMIZ2. Using Wnt3a-conditioned medium, we demonstrated that ZMIZ2 can enhance Wnt ligand-induced TCF/-catenin-mediated transcription. We also showed a promotional role of ZMIZ2 in enhancing -catenin downstream target gene expression in human cells and in Zmiz2 null (Zmiz2(-/-)) mouse embryonic fibroblasts (MEFs). The regulatory role of Zmiz2 in Wnt-induced TCF/-catenin-mediated transcription can be restored in Zmiz2(-/-) MEFs that were infected with adenoviral expression vectors for Zmiz2. Moreover, enhancement of Zmiz2 on TCF/-catenin-mediated transcription was further demonstrated in Zmiz2 knockout and Axin2 reporter compound mice. Furthermore, the protein-protein interaction between ZMIZ2 and -catenin was identified by co-immunoprecipitation and in vitro protein pulldown assays. We also observed recruitment of endogenous ZMIZ2 onto the promoter region of the Axin 2 gene, a -catenin downstream target promoter, in a Wnt ligand-inducible manner. Finally, a promotional role of ZMIZ2 on cell growth was demonstrated in human cell lines and Zmiz2 knockout MEFs. Our findings demonstrate a novel interaction between ZMIZ2 and -catenin and elucidate a novel mechanism for PIAS-like proteins in regulating Wnt signaling pathways.
引用
收藏
页码:35913 / 35924
页数:12
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