Back to Search Start Over

Oxygen level regulates N-terminal translation elongation of selected proteins through deoxyhypusine hydroxylation.

Authors :
Zhang, Yugang
Su, Dan
Zhu, Julia
Wang, Miao
Zhang, Yandong
Fu, Qin
Zhang, Sheng
Lin, Hening
Source :
Cell Reports; May2022, Vol. 39 Issue 8, pN.PAG-N.PAG, 1p
Publication Year :
2022

Abstract

Hypusine is a post-translational modification on eukaryotic translation initiation factor 5A (eIF5A). The last step of hypusine biosynthesis, deoxyhypusine hydroxylation, is an oxygen-dependent reaction. Here we show that deletion of the deoxyhypusine hydroxylase Lia1 compromises yeast respiration through translation downregulation of selected proteins in the respiration pathway. The translation suppression, because of the lack of deoxyhypusine hydroxylation, mainly affects translation of the N termini of the proteins, independent of the presence of proline residues but likely dependent on the interaction between the N-terminal nascent peptide and the ribosomal peptide exit tunnel. Proteomics and biochemical studies reveal that Lia1 deletion decreases N-terminal translation of proteins involved in mitochondrial respiration, oxidative stress response, and protein folding. Our work uncovers functions of the hypusine modification by considering the substrate requirement of the post-translational modification, highlights the unique challenges of translating the N termini of proteins, and reveals an oxygen-sensing mechanism in eukaryotic cells. [Display omitted] • eIF5A deoxyhypusine hydroxylation is an oxygen-sensing mechanism • Hydroxylation facilitates N-terminal translation of selected proteins • Hydroxylation promotes oxidative metabolism and survival Cells have to regulate their metabolism in response to oxygen levels. Zhang et al. find that oxygen regulates hydroxylation of translation factor eIF5A in yeast. Hydroxylation promotes translation of the N termini of many proteins essential for cell survival in the presence of oxygen in a proline-independent manner. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
26391856
Volume :
39
Issue :
8
Database :
Complementary Index
Journal :
Cell Reports
Publication Type :
Academic Journal
Accession number :
157032599
Full Text :
https://doi.org/10.1016/j.celrep.2022.110855