1. Academic Validation
  2. MAP4K Interactome Reveals STRN4 as a Key STRIPAK Complex Component in Hippo Pathway Regulation

MAP4K Interactome Reveals STRN4 as a Key STRIPAK Complex Component in Hippo Pathway Regulation

  • Cell Rep. 2020 Jul 7;32(1):107860. doi: 10.1016/j.celrep.2020.107860.
Gayoung Seo 1 Han Han 1 Rebecca Elizabeth Vargas 1 Bing Yang 1 Xu Li 2 Wenqi Wang 3
Affiliations

Affiliations

  • 1 Department of Developmental and Cell Biology, University of California, Irvine, Irvine, CA 92697, USA.
  • 2 School of Life Sciences, Westlake University, Hangzhou, Zhejiang Province 310024, China. Electronic address: [email protected].
  • 3 Department of Developmental and Cell Biology, University of California, Irvine, Irvine, CA 92697, USA. Electronic address: [email protected].
Abstract

Mitogen-activated protein kinase kinase kinase kinases (MAP4Ks) constitute a mammalian STE20-like serine/threonine kinase subfamily. Recent studies provide substantial evidence for MAP4K family kinases in the Hippo pathway regulation, suggesting a broad role of MAP4Ks in human physiology and diseases. However, a comprehensive analysis of the regulators and effectors for this key kinase family has not been fully achieved. Using a proteomic approach, we define the protein-protein interaction network for human MAP4K family kinases and reveal diverse cellular signaling events involving this important kinase family. Through it, we identify a STRIPAK complex component, STRN4, as a generic binding partner for MAP4Ks and a key regulator of the Hippo pathway in endometrial Cancer development. Taken together, the results of our study not only generate a rich resource for further characterizing human MAP4K family kinases in numerous biological processes but also dissect the STRIPAK-mediated regulation of MAP4Ks in the Hippo pathway.

Keywords

Hippo pathway; MAP4K; STRIPAK; STRN4; YAP; endometrial cancer; proteomics.

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