» Articles » PMID: 35658031

Ethylene Modulates Translation Dynamics in Under Submergence Via GCN2 and EIN2

Overview
Journal Sci Adv
Specialties Biology
Science
Date 2022 Jun 3
PMID 35658031
Authors
Affiliations
Soon will be listed here.
Abstract

General translational repression is a key process that reduces energy consumption under hypoxia. Here, we show that plant stress-activated general control nonderepressible 2 (GCN2) was activated to regulate the reduction in polysome loading during submergence in . GCN2 signaling was activated by ethylene under submergence. GCN2 activity was reduced in , but not in or , under submergence, suggesting that GCN2 activity is regulated by a noncanonical ethylene signaling pathway. Polysome loading was not reduced in under submergence, implying that ethylene modulates translation via both EIN2 and GCN2. Transcriptomic analysis demonstrated that EIN2 and GCN2 regulate not only general translational repression but also translational enhancement of specific mRNAs under submergence. Together, these results demonstrate that during submergence, entrapped ethylene triggers GCN2 and EIN2 to regulate translation dynamics and ensure the translation of stress response proteins.

Citing Articles

Primed to persevere: Hypoxia regulation from epigenome to protein accumulation in plants.

Gibbs D, Theodoulou F, Bailey-Serres J Plant Physiol. 2024; 197(1).

PMID: 39479777 PMC: 11663586. DOI: 10.1093/plphys/kiae584.


New Insights into the Connections between Flooding/Hypoxia Response and Plant Defenses against Pathogens.

Garcia P, Singh S, Graciet E Plants (Basel). 2024; 13(16).

PMID: 39204612 PMC: 11358971. DOI: 10.3390/plants13162176.


The phosphorylation of carboxyl-terminal eIF2α by SPA kinases contributes to enhanced translation efficiency during photomorphogenesis.

Chang H, Huang L, Browning K, Huq E, Cheng M Nat Commun. 2024; 15(1):3467.

PMID: 38658612 PMC: 11043401. DOI: 10.1038/s41467-024-47848-7.


A proxitome-RNA-capture approach reveals that processing bodies repress coregulated hub genes.

Liu C, Mentzelopoulou A, Hatzianestis I, Tzagkarakis E, Skaltsogiannis V, Ma X Plant Cell. 2023; 36(3):559-584.

PMID: 37971938 PMC: 10896293. DOI: 10.1093/plcell/koad288.


What, where, and how: Regulation of translation and the translational landscape in plants.

Wu H, Jen J, Hsu P Plant Cell. 2023; 36(5):1540-1564.

PMID: 37437121 PMC: 11062462. DOI: 10.1093/plcell/koad197.


References
1.
Thoreen C, Chantranupong L, Keys H, Wang T, Gray N, Sabatini D . A unifying model for mTORC1-mediated regulation of mRNA translation. Nature. 2012; 485(7396):109-13. PMC: 3347774. DOI: 10.1038/nature11083. View

2.
Cho H, Wen T, Wang Y, Shih M . Quantitative phosphoproteomics of protein kinase SnRK1 regulated protein phosphorylation in Arabidopsis under submergence. J Exp Bot. 2016; 67(9):2745-60. PMC: 4861021. DOI: 10.1093/jxb/erw107. View

3.
Merchante C, Brumos J, Yun J, Hu Q, Spencer K, Enriquez P . Gene-specific translation regulation mediated by the hormone-signaling molecule EIN2. Cell. 2015; 163(3):684-97. DOI: 10.1016/j.cell.2015.09.036. View

4.
Fahling M . Surviving hypoxia by modulation of mRNA translation rate. J Cell Mol Med. 2009; 13(9A):2770-9. PMC: 4498934. DOI: 10.1111/j.1582-4934.2009.00875.x. View

5.
Taniuchi S, Miyake M, Tsugawa K, Oyadomari M, Oyadomari S . Integrated stress response of vertebrates is regulated by four eIF2α kinases. Sci Rep. 2016; 6:32886. PMC: 5025754. DOI: 10.1038/srep32886. View