Crosstalk between translation and the aggresome–autophagy pathway

Yeonkyoung Park, Joori Park, Yoon Ki Kim

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Many neurodegenerative disorders feature the presence of misfolded polypeptide-containing intracellular inclusion bodies biochemically and morphologically analogous to cellular aggresomes. However, it is largely unknown how misfolded polypeptides form aggresomes and are eventually cleared by the aggresome-macroautophagy/autophagy pathway, so-called aggrephagy. Our recent study revealed that when the ubiquitin-proteasome system is impaired, the accumulated misfolded polypeptides are selectively recognized and transported to the aggresome by a CED complex. This complex is composed of CTIF, originally identified as a specific factor for nuclear cap-binding protein complex (a heterodimer of NCBP1/CBP80 and NCBP2/CBP20)-dependent translation (CT), and its associated factors EEF1A1 and DCTN1. Aggresomal targeting of a misfolded polypeptide via the CED complex is accompanied by CTIF release from the CT complex and thereby inhibits CT efficiency. Therefore, our study provides new mechanistic insights into the crosstalk between translational inhibition and aggresome formation under the influence of a misfolded polypeptide.

Original languageEnglish
Pages (from-to)1-3
Number of pages3
JournalAutophagy
DOIs
Publication statusAccepted/In press - 2017 Nov 1

Fingerprint

Peptides
Autophagy
Nuclear Cap-Binding Protein Complex
Inclusion Bodies
Proteasome Endopeptidase Complex
Ubiquitin
Neurodegenerative Diseases

Keywords

  • aggrephagy
  • aggresome
  • autophagy
  • CTIF
  • DCTN1
  • EEF1A1
  • misfolded polypeptide
  • NCBP1/CBP80
  • NCBP2/CBP20

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology

Cite this

Crosstalk between translation and the aggresome–autophagy pathway. / Park, Yeonkyoung; Park, Joori; Kim, Yoon Ki.

In: Autophagy, 01.11.2017, p. 1-3.

Research output: Contribution to journalArticle

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