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TEAD/TEF transcription factors utilize the activation domain of YAP65, a Src/Yes-associated protein localized in the cytoplasm

机译:TEAD / TEF转录因子利用YAP65的激活域,YAP65是一种位于细胞质中的Src / Yes相关蛋白

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摘要

Mammals express four highly conserved TEAD/TEF transcription factors that bind the same DNA sequence, but serve different functions during development. TEAD-2/TEF-4 protein purified from mouse cells was associated predominantly with a novel TEAD-binding domain at the amino terminus of YAP65, a powerful transcriptional coactivator. YAP65 interacted specifically with the carboxyl terminus of all four TEAD proteins. Both this interaction and sequence-specific DNA binding by TEAD were required for transcriptional activation in mouse cells. Expression of YAP in lymphocytic cells that normally do not support TEAD-dependent transcription (e.g., MPC11) resulted in up to 300-fold induction of TEAD activity. Conversely, TEAD overexpression squelched YAP activity. Therefore, the carboxy-terminal acidic activation domain in YAP is the transcriptional activation domain for TEAD transcription factors. However, whereas TEAD was concentrated in the nucleus, excess YAP65 accumulated in the cytoplasm as a complex with the cytoplasmic localization protein, 14-3-3. Because TEAD-dependent transcription was limited by YAP65, and YAP65 also binds Src/Yes protein tyrosine kinases, we propose that YAP65 regulates TEAD-dependent transcription in response to mitogenic signals.
机译:哺乳动物表达了四个高度保守的TEAD / TEF转录因子,它们结合相同的DNA序列,但在发育过程中发挥不同的功能。从小鼠细胞中纯化的TEAD-2 / TEF-4蛋白主要与YAP65(一种功能强大的转录共激活因子)的氨基末端的新型TEAD结合结构域相关。 YAP65与所有四个TEAD蛋白的羧基末端特异性相互作用。 TEAD的这种相互作用和序列特异性DNA结合都是小鼠细胞转录激活所必需的。 YAP在通常不支持TEAD依赖性转录的淋巴细胞(例如MPC11)中的表达可导致多达300倍的TEAD活性诱导。相反,TEAD过度表达抑制了YAP活动。因此,YAP中的羧基末端酸性激活域是TEAD转录因子的转录激活域。但是,尽管TEAD集中在细胞核中,但过量的YAP65却与细胞质定位蛋白14-3-3形成复合物。由于TEAD依赖的转录受到YAP65的限制,并且YAP65也结合Src / Yes蛋白酪氨酸激酶,因此我们建议YAP65调节有丝分裂信号对TEAD的依赖转录。

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