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MRTF增强TEAD-YAP转录活性,导致转移。

MRTF potentiates TEAD-YAP transcriptional activity causing metastasis.

作者信息

Kim Tackhoon, Hwang Daehee, Lee Dahye, Kim Jeong-Hwan, Kim Seon-Young, Lim Dae-Sik

机构信息

National Creative Research Initiatives Center for Cell Division and Differentiation, Department of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Korea

National Creative Research Initiatives Center for Cell Division and Differentiation, Department of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Korea.

出版信息

EMBO J. 2017 Feb 15;36(4):520-535. doi: 10.15252/embj.201695137. Epub 2016 Dec 27.

Abstract

Yes-associated protein (YAP) and myocardin-related transcription factor (MRTF) play similar roles and exhibit significant crosstalk in directing transcriptional responses to chemical and physical extracellular cues. The mechanism underlying this crosstalk, however, remains unclear. Here, we show MRTF family proteins bind YAP via a conserved PPXY motif that interacts with the YAP WW domain. This interaction allows MRTF to recruit NcoA3 to the TEAD-YAP transcriptional complex and potentiate its transcriptional activity. We show this interaction of MRTF and YAP is critical for LPA-induced cancer cell invasion and breast cancer metastasis to the lung We also demonstrate the significance of MRTF-YAP binding in regulation of YAP activity upon acute actin cytoskeletal damage. Acute actin disruption induces nucleo-cytoplasmic shuttling of MRTF, and this process underlies the LATS-independent regulation of YAP activity. Our results provide clear evidence of crosstalk between MRTF and YAP independent of the LATS kinases that normally act upstream of YAP signaling. Our results also suggest a mechanism by which extracellular stimuli can coordinate physiological events downstream of YAP.

摘要

Yes相关蛋白(YAP)和心肌相关转录因子(MRTF)在指导对化学和物理细胞外信号的转录反应中发挥相似作用并表现出显著的相互作用。然而,这种相互作用背后的机制仍不清楚。在这里,我们表明MRTF家族蛋白通过与YAP WW结构域相互作用的保守PPXY基序结合YAP。这种相互作用使MRTF能够将NcoA3募集到TEAD-YAP转录复合物并增强其转录活性。我们表明MRTF与YAP的这种相互作用对于溶血磷脂酸(LPA)诱导的癌细胞侵袭以及乳腺癌转移至肺部至关重要。我们还证明了MRTF-YAP结合在急性肌动蛋白细胞骨架损伤后对YAP活性调节中的重要性。急性肌动蛋白破坏诱导MRTF的核质穿梭,并且这个过程是YAP活性不依赖于大肿瘤抑制激酶1(LATS)的调节基础。我们的结果提供了MRTF和YAP之间相互作用的明确证据,该相互作用独立于通常在YAP信号上游起作用的LATS激酶。我们的结果还提出了一种细胞外刺激可以协调YAP下游生理事件的机制。

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