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在发育和疾病中,YAP1通过mRNA剪接异构体进行离散信号传导模式的证据。

Evidence for discrete modes of YAP1 signaling via mRNA splice isoforms in development and diseases.

作者信息

Vrbský Jan, Vinarský Vladimir, Perestrelo Ana Rubina, De La Cruz Jorge Oliver, Martino Fabiana, Pompeiano Antonio, Izzi Valerio, Hlinomaz Ota, Rotrekl Vladimir, Sudol Marius, Pagliari Stefania, Forte Giancarlo

机构信息

International Clinical Research Center (ICRC), St Anne's University Hospital, CZ-65691 Brno, Czech Republic.

International Clinical Research Center (ICRC), St Anne's University Hospital, CZ-65691 Brno, Czech Republic; Competence Center for Mechanobiology in Regenerative Medicine, INTERREG ATCZ133, CZ-62500 Brno, Czech Republic.

出版信息

Genomics. 2021 May;113(3):1349-1365. doi: 10.1016/j.ygeno.2021.03.009. Epub 2021 Mar 11.

Abstract

Yes-associated protein 1 (YAP1) is a transcriptional co-activator downstream of Hippo pathway. The pathway exerts crucial roles in organogenesis and its dysregulation is associated with the spreading of different cancer types. YAP1 gene encodes for multiple protein isoforms, whose specific functions are not well defined. We demonstrate the splicing of isoform-specific mRNAs is controlled in a stage- and tissue-specific fashion. We designed expression vectors encoding for the most-represented isoforms of YAP1 with either one or two WW domains and studied their specific signaling activities in YAP1 knock-out cell lines. YAP1 isoforms display both common and unique functions and activate distinct transcriptional programs, as the result of their unique protein interactomes. By generating TEAD-based transcriptional reporter cell lines, we demonstrate individual YAP1 isoforms display unique effects on cell proliferation and differentiation. Finally, we illustrate the complexity of the regulation of Hippo-YAP1 effector in physiological and in pathological conditions of the heart.

摘要

Yes相关蛋白1(YAP1)是Hippo信号通路下游的一种转录共激活因子。该信号通路在器官发生过程中发挥关键作用,其失调与多种癌症类型的扩散有关。YAP1基因编码多种蛋白质异构体,其具体功能尚未明确界定。我们证明,异构体特异性mRNA的剪接是以阶段和组织特异性方式受到调控的。我们设计了表达载体,编码具有一个或两个WW结构域的YAP1最具代表性的异构体,并研究了它们在YAP1基因敲除细胞系中的特定信号传导活性。由于其独特的蛋白质相互作用组,YAP1异构体表现出共同和独特的功能,并激活不同的转录程序。通过构建基于TEAD的转录报告细胞系,我们证明单个YAP1异构体对细胞增殖和分化具有独特影响。最后,我们阐述了在心脏生理和病理条件下Hippo-YAP1效应器调控的复杂性。

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