The eIF2a serine 51 phosphorylation-ATF4 arm promotes HIPPO signaling and cell death under oxidative stress

Kamindla Rajesh, Jothilatha Krishnamoorthy, Jyotsana Gupta, Urszula Kazimierczak, Andreas I. Papadakis, Zhilin Deng, Shuo Wang, Shinji Kuninaka, Antonis E. Koromilas

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

The HIPPO pathway is an evolutionary conserved regulator of organ size that controls both cell proliferation and death. This pathway has an important role in mediating cell death in response to oxidative stress through the inactivation of Yes-associated protein (YAP) and inhibition of anti-oxidant gene expression. Cells exposed to oxidative stress induce the phosphorylation of the alpha (a) subunit of the translation initiation factor eIF2 at serine 51 (eIF2αP), a modification that leads to the general inhibition of mRNA translation initiation. Under these conditions, increased eIF2αP facilitates the mRNA translation of activating transcription factor 4 (ATF4), which mediates either cell survival and adaptation or cell death under conditions of severe stress. Herein, we demonstrate a functional connection between the HIPPO and eIF2αP-ATF4 pathways under oxidative stress. We demonstrate that ATF4 promotes the stabilization of the large tumor suppressor 1 (LATS1), which inactivates YAP by phosphorylation. ATF4 inhibits the expression of NEDD4.2 and WWP1 mRNAs under pro-oxidant conditions, which encode ubiquitin ligases mediating the proteasomal degradation of LATS1. Increased LATS1 stability is required for the induction of cell death under oxidative stress. Our data reveal a previously unidentified ATF4-dependent pathway in the induction of cell death under oxidative stress via the activation of LATS1 and HIPPO pathway.

Original languageEnglish
Pages (from-to)51044-51058
Number of pages15
JournalOncotarget
Volume7
Issue number32
DOIs
Publication statusPublished - 2016 Aug 1

Fingerprint

Activating Transcription Factor 4
Serine
Oxidative Stress
Cell Death
Phosphorylation
Protein Biosynthesis
Neoplasms
Peptide Initiation Factors
Organ Size
Ligases
Ubiquitin
Oxidants
Reactive Oxygen Species
Cell Survival
Proteins
Cell Proliferation
Gene Expression
Messenger RNA

Keywords

  • Activating transcription factor 4
  • Large tumor suppressor 1
  • MRNA translation
  • Protein phosphorylation
  • Translation initiation factor eIF2

ASJC Scopus subject areas

  • Oncology

Cite this

Rajesh, K., Krishnamoorthy, J., Gupta, J., Kazimierczak, U., Papadakis, A. I., Deng, Z., ... Koromilas, A. E. (2016). The eIF2a serine 51 phosphorylation-ATF4 arm promotes HIPPO signaling and cell death under oxidative stress. Oncotarget, 7(32), 51044-51058. https://doi.org/10.18632/oncotarget.10480

The eIF2a serine 51 phosphorylation-ATF4 arm promotes HIPPO signaling and cell death under oxidative stress. / Rajesh, Kamindla; Krishnamoorthy, Jothilatha; Gupta, Jyotsana; Kazimierczak, Urszula; Papadakis, Andreas I.; Deng, Zhilin; Wang, Shuo; Kuninaka, Shinji; Koromilas, Antonis E.

In: Oncotarget, Vol. 7, No. 32, 01.08.2016, p. 51044-51058.

Research output: Contribution to journalArticle

Rajesh, K, Krishnamoorthy, J, Gupta, J, Kazimierczak, U, Papadakis, AI, Deng, Z, Wang, S, Kuninaka, S & Koromilas, AE 2016, 'The eIF2a serine 51 phosphorylation-ATF4 arm promotes HIPPO signaling and cell death under oxidative stress', Oncotarget, vol. 7, no. 32, pp. 51044-51058. https://doi.org/10.18632/oncotarget.10480
Rajesh K, Krishnamoorthy J, Gupta J, Kazimierczak U, Papadakis AI, Deng Z et al. The eIF2a serine 51 phosphorylation-ATF4 arm promotes HIPPO signaling and cell death under oxidative stress. Oncotarget. 2016 Aug 1;7(32):51044-51058. https://doi.org/10.18632/oncotarget.10480
Rajesh, Kamindla ; Krishnamoorthy, Jothilatha ; Gupta, Jyotsana ; Kazimierczak, Urszula ; Papadakis, Andreas I. ; Deng, Zhilin ; Wang, Shuo ; Kuninaka, Shinji ; Koromilas, Antonis E. / The eIF2a serine 51 phosphorylation-ATF4 arm promotes HIPPO signaling and cell death under oxidative stress. In: Oncotarget. 2016 ; Vol. 7, No. 32. pp. 51044-51058.
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