1. Academic Validation
  2. Human oncoprotein 5MP suppresses general and repeat-associated non-AUG translation via eIF3 by a common mechanism

Human oncoprotein 5MP suppresses general and repeat-associated non-AUG translation via eIF3 by a common mechanism

  • Cell Rep. 2021 Jul 13;36(2):109376. doi: 10.1016/j.celrep.2021.109376.
Chingakham Ranjit Singh 1 M Rebecca Glineburg 2 Chelsea Moore 1 Naoki Tani 3 Rahul Jaiswal 4 Ye Zou 5 Eric Aube 1 Sarah Gillaspie 1 Mackenzie Thornton 1 Ariana Cecil 1 Madelyn Hilgers 1 Azuma Takasu 1 Izumi Asano 1 Masayo Asano 1 Carlos R Escalante 4 Akira Nakamura 3 Peter K Todd 6 Katsura Asano 7
Affiliations

Affiliations

  • 1 Molecular Cellular and Developmental Biology Program, Division of Biology, Kansas State University, Manhattan, KS 66506, USA.
  • 2 Department of Neurology, University of Michigan, Ann Arbor, MI 48109, USA.
  • 3 Institute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto 860-0811, Japan.
  • 4 Department of Physiology and Biophysics, Virginia Commonwealth University, School of Medicine, Richmond, VA 23298, USA.
  • 5 Department of Biochemistry and Molecular Biophysics, Kansas State University, Manhattan, KS 66506, USA.
  • 6 Department of Neurology, University of Michigan, Ann Arbor, MI 48109, USA; Ann Arbor VA Medical Center, Ann Arbor, MI 48105, USA.
  • 7 Molecular Cellular and Developmental Biology Program, Division of Biology, Kansas State University, Manhattan, KS 66506, USA; Graduate School of Integrated Sciences for Life, Hiroshima University, Higashi-Hiroshima, Hiroshima 739-8530, Japan; Hiroshima Research Center for Healthy Aging, Hiroshima University, Higashi-Hiroshima, Hiroshima 739-8530, Japan. Electronic address: [email protected].
Abstract

eIF5-mimic protein (5MP) is a translational regulatory protein that binds the small ribosomal subunit and modulates its activity. 5MP is proposed to reprogram non-AUG translation rates for oncogenes in Cancer, but its role in controlling non-AUG initiated synthesis of deleterious repeat-peptide products, such as FMRpolyG observed in fragile-X-associated tremor ataxia syndrome (FXTAS), is unknown. Here, we show that 5MP can suppress both general and repeat-associated non-AUG (RAN) translation by a common mechanism in a manner dependent on its interaction with eIF3. Essentially, 5MP displaces eIF5 through the eIF3c subunit within the preinitiation complex (PIC), thereby increasing the accuracy of initiation. In Drosophila, 5MP/Kra represses neuronal toxicity and enhances the lifespan in an FXTAS disease model. These results implicate 5MP in protecting cells from unwanted byproducts of non-AUG translation in neurodegeneration.

Keywords

FXTAS; RAN translation; cancer; eIF5-mimic protein; non-AUG start codon; ribosome; translation initiation.

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