Nuclear Matrix Protein 4 Is a Novel Regulator of Ribosome Biogenesis and Controls the Unfolded Protein Response via Repression of Gadd34 Expression

Abstract

The unfolded protein response (UPR) maintains protein homeostasis by governing the processing capacity of the endoplasmic reticulum (ER) to manage ER client loads; however, key regulators within the UPR remain to be identified. Activation of the UPR sensor PERK (EIFAK3/PEK) results in the phosphorylation of thex2; alpha subunit of eIF2 (eIF2alphax2;-P), which represses translation initiation and reduces influx of newly synthesized proteins into the overloaded ER. As part of this adaptive response, eIF2alphax2;-P also induces a feedback mechanism through enhanced transcriptional and translational expression of Gadd34 (Ppp1r15A), which targets type 1 protein phosphatase for dephosphorylation of eIF2alphax2;-P to restore protein synthesis. Here we describe a novel mechanism by which Gadd34 expression is regulated through the activity of the zinc finger transcription factor NMP4 (ZNF384, CIZ). NMP4 functions to suppress bone anabolism, and we suggest that this occurs due to decreased protein synthesis of factors involved in bone formation through NMP4-mediated dampening of Gadd34 and c-Myc expression. Loss of Nmp4 resulted in an increase in c-Myc and Gadd34 expression that facilitated enhanced ribosome biogenesis and global protein synthesis. Importantly, protein synthesis was sustained during pharmacological induction of the UPR through a mechanism suggested to involve GADD34-mediated dephosphorylation of eIF2alphax2;-P. Sustained protein synthesis sensitized cells to pharmacological induction of the UPR, and the observed decrease in cell viability was restored upon inhibition of GADD34 activity. We conclude that NMP4 is a key regulator of ribosome biogenesis and the UPR, which together play a central role in determining cell viability during endoplasmic reticulum stress.

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Document Details

Document Type
Technical Report
Publication Date
Apr 29, 2016
Accession Number
AD1038912

Entities

People

  • Joseph P. Bidwell
  • Ronald C. Wek
  • Sara K. Young
  • Yu Shao

Organizations

  • Indiana University

Tags

DTIC Thesaurus Topics

  • Biochemistry
  • Biology
  • Blood Cells
  • Bone Marrow
  • Cell Physiological Processes
  • Cells
  • Chemistry
  • Endoplasmic Reticulum
  • Endoplasmic Reticulum Stress
  • Genetics
  • Intranuclear Space
  • Metabolism
  • Molecular Biology
  • Organelles
  • Osteogenesis
  • Phosphorylation
  • Proteins
  • Proteomics
  • Stem Cells
  • Stress (Physiology)
  • Therapeutics
  • Tissues
  • Transcription Factors

Fields of Study

  • Biology

Readers

  • Cellular and Molecular Pathways of Apoptosis.
  • Molecular Biology and Genetics