Literature DB >> 33049316

Dystonia 16 (DYT16) mutations in PACT cause dysregulated PKR activation and eIF2α signaling leading to a compromised stress response.

Samuel B Burnett1, Lauren S Vaughn1, Nutan Sharma2, Ronit Kulkarni1, Rekha C Patel3.   

Abstract

Dystonia 16 (DYT16) is caused by mutations in PACT, the protein activator of interferon-induced double-stranded RNA-activated protein kinase (PKR). PKR regulates the integrated stress response (ISR) via phosphorylation of the translation initiation factor eIF2α. This post-translational modification attenuates general protein synthesis while concomitantly triggering enhanced translation of a few specific transcripts leading either to recovery and homeostasis or cellular apoptosis depending on the intensity and duration of stress signals. PKR plays a regulatory role in determining the cellular response to viral infections, oxidative stress, endoplasmic reticulum (ER) stress, and growth factor deprivation. In the absence of stress, both PACT and PKR are bound by their inhibitor transactivation RNA-binding protein (TRBP) thereby keeping PKR inactive. Under conditions of cellular stress these inhibitory interactions dissociate facilitating PACT-PACT interactions critical for PKR activation. While both PACT-TRBP and PKR-TRBP interactions are pro-survival, PACT-PACT and PACT-PKR interactions are pro-apoptotic. In this study we evaluate if five DYT16 substitution mutations alter PKR activation and ISR. Our results indicate that the mutant DYT16 proteins show stronger PACT-PACT interactions and enhanced PKR activation. In DYT16 patient derived lymphoblasts the enhanced PACT-PKR interactions and heightened PKR activation leads to a dysregulation of ISR and increased apoptosis. More importantly, this enhanced sensitivity to ER stress can be rescued by luteolin, which disrupts PACT-PKR interactions. Our results not only demonstrate the impact of DYT16 mutations on regulation of ISR and DYT16 etiology but indicate that therapeutic interventions could be possible after a further evaluation of such strategies.
Copyright © 2020 The Author(s). Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  DYT16; Dystonia 16; ISR; PACT; PKR; Prkra; eIF2α

Year:  2020        PMID: 33049316     DOI: 10.1016/j.nbd.2020.105135

Source DB:  PubMed          Journal:  Neurobiol Dis        ISSN: 0969-9961            Impact factor:   5.996


  6 in total

1.  DYT-PRKRA Mutation P222L Enhances PACT's Stimulatory Activity on Type I Interferon Induction.

Authors:  Lauren S Vaughn; Kenneth Frederick; Samuel B Burnett; Nutan Sharma; D Cristopher Bragg; Sarah Camargos; Francisco Cardoso; Rekha C Patel
Journal:  Biomolecules       Date:  2022-05-17

Review 2.  Cellular origins of dsRNA, their recognition and consequences.

Authors:  Y Grace Chen; Sun Hur
Journal:  Nat Rev Mol Cell Biol       Date:  2021-11-23       Impact factor: 113.915

Review 3.  Innate Immunity: A Balance between Disease and Adaption to Stress.

Authors:  Irene Faenza; William L Blalock
Journal:  Biomolecules       Date:  2022-05-23

4.  Opposite actions of two dsRNA-binding proteins PACT and TRBP on RIG-I mediated signaling.

Authors:  Lauren S Vaughn; Evelyn Chukwurah; Rekha C Patel
Journal:  Biochem J       Date:  2021-02-12       Impact factor: 3.857

5.  EIF2AK2 Missense Variants Associated with Early Onset Generalized Dystonia.

Authors:  Demy J S Kuipers; Wim Mandemakers; Chin-Song Lu; Simone Olgiati; Guido J Breedveld; Christina Fevga; Vera Tadic; Miryam Carecchio; Bradley Osterman; Lena Sagi-Dain; Yah-Huei Wu-Chou; Chiung C Chen; Hsiu-Chen Chang; Shey-Lin Wu; Tu-Hsueh Yeh; Yi-Hsin Weng; Antonio E Elia; Celeste Panteghini; Nicolas Marotta; Martje G Pauly; Andrea A Kühn; Jens Volkmann; Baiba Lace; Inge A Meijer; Krishna Kandaswamy; Marialuisa Quadri; Barbara Garavaglia; Katja Lohmann; Peter Bauer; Niccolò E Mencacci; Steven J Lubbe; Christine Klein; Aida M Bertoli-Avella; Vincenzo Bonifati
Journal:  Ann Neurol       Date:  2020-12-15       Impact factor: 10.422

6.  Uniparental disomy screen of Irish rare disorder cohort unmasks homozygous variants of clinical significance in the TMCO1 and PRKRA genes.

Authors:  B Molloy; E R Jones; N D Linhares; P G Buckley; T R Leahy; B Lynch; I Knerr; M D King; K M Gorman
Journal:  Front Genet       Date:  2022-09-14       Impact factor: 4.772

  6 in total

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