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本文引用的文献

1
Structural basis of YAP recognition by TEAD4 in the hippo pathway.YAP 通过 TEAD4 在 Hippo 通路中识别的结构基础。
Genes Dev. 2010 Feb 1;24(3):290-300. doi: 10.1101/gad.1865310.
2
Structural insights into the YAP and TEAD complex.YAP 和 TEAD 复合物的结构见解。
Genes Dev. 2010 Feb 1;24(3):235-40. doi: 10.1101/gad.1865810.
3
A coordinated phosphorylation by Lats and CK1 regulates YAP stability through SCF(beta-TRCP).Lats 和 CK1 的协调磷酸化通过 SCF(beta-TRCP) 调节 YAP 的稳定性。
Genes Dev. 2010 Jan 1;24(1):72-85. doi: 10.1101/gad.1843810.
4
Suppression of induced pluripotent stem cell generation by the p53-p21 pathway.p53-p21 通路对诱导多能干细胞生成的抑制作用。
Nature. 2009 Aug 27;460(7259):1132-5. doi: 10.1038/nature08235. Epub 2009 Aug 9.
5
Linking the p53 tumour suppressor pathway to somatic cell reprogramming.将p53肿瘤抑制通路与体细胞重编程联系起来。
Nature. 2009 Aug 27;460(7259):1140-4. doi: 10.1038/nature08311. Epub 2009 Aug 9.
6
Yes-associated protein is an independent prognostic marker in hepatocellular carcinoma.Yes相关蛋白是肝细胞癌中的一个独立预后标志物。
Cancer. 2009 Oct 1;115(19):4576-85. doi: 10.1002/cncr.24495.
7
The Hippo signaling pathway components Lats and Yap pattern Tead4 activity to distinguish mouse trophectoderm from inner cell mass.河马信号通路的组成部分Lats和Yap调控Tead4的活性,以区分小鼠滋养外胚层和内细胞团。
Dev Cell. 2009 Mar;16(3):398-410. doi: 10.1016/j.devcel.2009.02.003.
8
Both TEAD-binding and WW domains are required for the growth stimulation and oncogenic transformation activity of yes-associated protein.Yes相关蛋白的生长刺激和致癌转化活性需要TEAD结合域和WW结构域。
Cancer Res. 2009 Feb 1;69(3):1089-98. doi: 10.1158/0008-5472.CAN-08-2997. Epub 2009 Jan 13.
9
Prdm proto-oncogene transcription factor family expression and interaction with the Notch-Hes pathway in mouse neurogenesis.Prdm原癌基因转录因子家族在小鼠神经发生中的表达及其与Notch-Hes信号通路的相互作用。
PLoS One. 2008;3(12):e3859. doi: 10.1371/journal.pone.0003859. Epub 2008 Dec 3.
10
YAP regulates neural progenitor cell number via the TEA domain transcription factor.YAP通过TEA结构域转录因子调节神经祖细胞数量。
Genes Dev. 2008 Dec 1;22(23):3320-34. doi: 10.1101/gad.1726608. Epub 2008 Nov 17.

YAP 转录共激活因子在调节干细胞自我更新和分化中的作用。

The role of YAP transcription coactivator in regulating stem cell self-renewal and differentiation.

机构信息

Moores Cancer Center, University of California at San Diego, La Jolla, California 92093, USA.

出版信息

Genes Dev. 2010 Jun 1;24(11):1106-18. doi: 10.1101/gad.1903310.

DOI:10.1101/gad.1903310
PMID:20516196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2878649/
Abstract

Yes-associated protein (YAP) is a potent transcription coactivator acting via binding to the TEAD transcription factor, and plays a critical role in organ size regulation. YAP is phosphorylated and inhibited by the Lats kinase, a key component of the Hippo tumor suppressor pathway. Elevated YAP protein levels and gene amplification have been implicated in human cancer. In this study, we report that YAP is inactivated during embryonic stem (ES) cell differentiation, as indicated by decreased protein levels and increased phosphorylation. Consistently, YAP is elevated during induced pluripotent stem (iPS) cell reprogramming. YAP knockdown leads to a loss of ES cell pluripotency, while ectopic expression of YAP prevents ES cell differentiation in vitro and maintains stem cell phenotypes even under differentiation conditions. Moreover, YAP binds directly to promoters of a large number of genes known to be important for stem cells and stimulates their expression. Our observations establish a critical role of YAP in maintaining stem cell pluripotency.

摘要

Yes 相关蛋白 (YAP) 是一种有效的转录共激活因子,通过与 TEAD 转录因子结合发挥作用,在器官大小调节中发挥关键作用。YAP 被 Lats 激酶磷酸化和抑制,Lats 激酶是 Hippo 肿瘤抑制途径的关键组成部分。YAP 蛋白水平升高和基因扩增与人类癌症有关。在这项研究中,我们报告说 YAP 在胚胎干细胞 (ES) 细胞分化过程中失活,表现为蛋白水平降低和磷酸化增加。一致地,YAP 在诱导多能干细胞 (iPS) 细胞重编程过程中升高。YAP 敲低导致 ES 细胞多能性丧失,而 YAP 的异位表达可防止 ES 细胞体外分化,并在分化条件下维持干细胞表型。此外,YAP 直接与大量已知对干细胞重要的基因的启动子结合,并刺激其表达。我们的观察结果确立了 YAP 在维持干细胞多能性中的关键作用。