Tead2 expression levels control the subcellular distribution of Yap and Taz, zyxin expression and epithelial-mesenchymal transition

被引:138
作者
Diepenbruck, Maren [1 ]
Waldmeier, Lorenz [1 ]
Ivanek, Robert [1 ]
Berninger, Philipp [2 ,3 ]
Arnold, Phil [2 ,3 ]
van Nimwegen, Erik [2 ,3 ]
Christofori, Gerhard [1 ]
机构
[1] Univ Basel, Dept Biomed, CH-4058 Basel, Switzerland
[2] Univ Basel, Biozentrum, CH-4056 Basel, Switzerland
[3] Swiss Inst Bioinformat, CH-4056 Basel, Switzerland
基金
瑞士国家科学基金会; 欧盟第七框架计划;
关键词
Breast cancer; EMT; metastasis; Taz; Tead; Yap; Zyxin; TRANSCRIPTION FACTORS; CELL-PROLIFERATION; ORGAN SIZE; CANCER; PATHWAY; ENHANCER; EMT; GROWTH; FAMILY; DIFFERENTIATION;
D O I
10.1242/jcs.139865
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The cellular changes during an epithelial-mesenchymal transition (EMT) largely rely on global changes in gene expression orchestrated by transcription factors. Tead transcription factors and their transcriptional co-activators Yap and Taz have been previously implicated in promoting an EMT; however, their direct transcriptional target genes and their functional role during EMT have remained elusive. We have uncovered a previously unanticipated role of the transcription factor Tead2 during EMT. During EMT in mammary gland epithelial cells and breast cancer cells, levels of Tead2 increase in the nucleus of cells, thereby directing a predominant nuclear localization of its co-factors Yap and Taz via the formation of Tead2-Yap-Taz complexes. Genome-wide chromatin immunoprecipitation and next generation sequencing in combination with gene expression profiling revealed the transcriptional targets of Tead2 during EMT. Among these, zyxin contributes to the migratory and invasive phenotype evoked by Tead2. The results demonstrate that Tead transcription factors are crucial regulators of the cellular distribution of Yap and Taz, and together they control the expression of genes critical for EMT and metastasis.
引用
收藏
页码:1523 / 1536
页数:14
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