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Salvador protein is a tumor suppressor effector of RASSF1A with hippo pathway-independent functions.

The RASSF1A tumor suppressor binds and activates proapoptotic MST kinases. The Salvador adaptor protein couples MST kinases to the LATS kinases to form the hippo pathway. Upon activation by RASSF1A, LATS1 phosphorylates the transcriptional regulator YAP, which binds to p73 and activates its proapoptotic effects. However, although serving as an adaptor for MST and LATS, Salvador can also bind RASSF1A. The functional role of the RASSF1A/Salvador interaction is unclear. Although Salvador is a novel tumor suppressor in Drosophila and mice, its role in human systems remains largely unknown. Here we show that Salvador promotes apoptosis in human cells and that Salvador inactivation deregulates the cell cycle and enhances the transformed phenotype. Moreover, we show that although the salvador gene is seldom mutated or epigenetically inactivated in human cancers, it is frequently down-regulated posttranscriptionally. Surprisingly, we also find that although RASSF1A requires the presence of Salvador for full apoptotic activity and to activate p73, this effect does not require a direct interaction of RASSF1A with MST kinases or the activation of the hippo pathway. Thus, we confirm a role for Salvador as a human tumor suppressor and RASSF1A effector and show that Salvador allows RASSF1A to modulate p73 independently of the hippo pathway.

Pubmed ID: 21489991

Authors

  • Donninger H
  • Allen N
  • Henson A
  • Pogue J
  • Williams A
  • Gordon L
  • Kassler S
  • Dunwell T
  • Latif F
  • Clark GJ

Journal

The Journal of biological chemistry

Publication Data

May 27, 2011

Associated Grants

  • Agency: NCRR NIH HHS, Id: RR18733
  • Agency: Cancer Research UK, Id:
  • Agency: Intramural NIH HHS, Id:

Mesh Terms

  • Animals
  • Apoptosis
  • Cell Cycle
  • Cell Cycle Proteins
  • Cell Line, Tumor
  • DNA-Binding Proteins
  • Drosophila melanogaster
  • HEK293 Cells
  • Humans
  • Mice
  • Nuclear Proteins
  • Phosphorylation
  • Protein Binding
  • Protein-Serine-Threonine Kinases
  • Signal Transduction
  • Transcription Factors
  • Tumor Suppressor Proteins