Literature DB >> 28634071

The novel YAP target gene, SGK1, upregulates TAZ activity by blocking GSK3β-mediated TAZ destabilization.

Geon Yoo1, Tackhoon Kim2, Chaeuk Chung3, Deog-Su Hwang1, Dae-Sik Lim4.   

Abstract

YAP (Yes-associated protein) and TAZ (transcription activator with PDZ binding motif) are important in tissue regeneration and cancer development, highlighting the importance of discovering partners that regulate their oncogenicity. SGK1 (serum/glucocorticoid regulated kinase 1), initially identified as a homolog of Akt in phosphoinositide 3-kinase signaling, acts as a serine/threonine protein kinase in multiple oncogenic pathways. However, possible links between SGK1 and Hippo-YAP/TAZ signaling remain unexplored. Here, we reveal that SGK1 is a potential positive feedback regulator of YAP and TAZ, showing that the TEAD-YAP/TAZ complex directly activates SGK1 transcription by binding to the distal enhancer of SGK1, and SGK1, in turn, stabilizes YAP/TAZ. Moreover, we demonstrate that expression of YAP/TAZ target genes is positively regulated by SGK1. Mechanistically, SGK1 inhibits ubiquitin-mediated degradation of TAZ by inhibiting GSK3β activity. These findings expand our understanding of YAP/TAZ regulation to include the novel downstream target of YAP, SGK1.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Hippo pathway; SGK1; TAZ; YAP

Mesh:

Substances:

Year:  2017        PMID: 28634071     DOI: 10.1016/j.bbrc.2017.06.092

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  6 in total

1.  Serum- and Glucocorticoid-induced Kinase Sgk1 Directly Promotes the Differentiation of Colorectal Cancer Cells and Restrains Metastasis.

Authors:  Lennard Y W Lee; Connor Woolley; Thomas Starkey; Sujata Biswas; Tia Mirshahi; Chiara Bardella; Stefania Segditsas; Shazia Irshad; Ian Tomlinson
Journal:  Clin Cancer Res       Date:  2018-10-15       Impact factor: 12.531

Review 2.  Hippo-Yap/Taz signaling: Complex network interactions and impact in epithelial cell behavior.

Authors:  Benjamin J van Soldt; Wellington V Cardoso
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2019-12-11

3.  IFN-γ-response mediator GBP-1 represses human cell proliferation by inhibiting the Hippo signaling transcription factor TEAD.

Authors:  Bea Unterer; Veit Wiesmann; Mekala Gunasekaran; Heinrich Sticht; Clara Tenkerian; Jürgen Behrens; Marina Leone; Felix B Engel; Nathalie Britzen-Laurent; Elisabeth Naschberger; Thomas Wittenberg; Michael Stürzl
Journal:  Biochem J       Date:  2018-09-25       Impact factor: 3.857

4.  Characterization of the Src-regulated kinome identifies SGK1 as a key mediator of Src-induced transformation.

Authors:  Xiuquan Ma; Luxi Zhang; Jiangning Song; Elizabeth Nguyen; Rachel S Lee; Samuel J Rodgers; Fuyi Li; Cheng Huang; Ralf B Schittenhelm; Howard Chan; Chanly Chheang; Jianmin Wu; Kristin K Brown; Christina A Mitchell; Kaylene J Simpson; Roger J Daly
Journal:  Nat Commun       Date:  2019-01-17       Impact factor: 14.919

5.  Yes-activated protein promotes primary resistance of BRAF V600E mutant metastatic colorectal cancer cells to mitogen-activated protein kinase pathway inhibitors.

Authors:  Meng Su; Lei Zhan; Yong Zhang; Jingdong Zhang
Journal:  J Gastrointest Oncol       Date:  2021-06

6.  The interaction of TEA domain transcription factor 4 (TEAD4) and Yes-associated protein 1 (YAP1) promoted the malignant process mediated by serum/glucocorticoid regulated kinase 1 (SGK1).

Authors:  Songlin He; Hanlu Zhang; Zongwei Xiao; Sandeep Bhushan; Ke Gao; Wenping Wang
Journal:  Bioengineered       Date:  2021-12       Impact factor: 3.269

  6 in total

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