Deciphering the mechanism of E3 ubiquitin ligases in plant responses to abiotic and biotic stresses and perspectives on PROTACs for crop resistance

Author:

Su Yingying1,Ngea Guillaume Legrand Ngolong12,Wang Kaili1,Lu Yuchun1,Godana Esa Abiso1,Ackah Michael1ORCID,Yang Qiya1,Zhang Hongyin1ORCID

Affiliation:

1. School of Food and Biological Engineering Jiangsu University Zhenjiang China

2. Institute of Fisheries Sciences, University of Douala Douala Cameroon

Abstract

SummaryWith global climate change, it is essential to find strategies to make crops more resistant to different stresses and guarantee food security worldwide. E3 ubiquitin ligases are critical regulatory elements that are gaining importance due to their role in selecting proteins for degradation in the ubiquitin‐proteasome proteolysis pathway. The role of E3 Ub ligases has been demonstrated in numerous cellular processes in plants responding to biotic and abiotic stresses. E3 Ub ligases are considered a class of proteins that are difficult to control by conventional inhibitors, as they lack a standard active site with pocket, and their biological activity is mainly due to protein–protein interactions with transient conformational changes. Proteolysis‐targeted chimeras (PROTACs) are a new class of heterobifunctional molecules that have emerged in recent years as relevant alternatives for incurable human diseases like cancer because they can target recalcitrant proteins for destruction. PROTACs interact with the ubiquitin‐proteasome system, principally the E3 Ub ligase in the cell, and facilitate proteasome turnover of the proteins of interest. PROTAC strategies harness the essential functions of E3 Ub ligases for proteasomal degradation of proteins involved in dysfunction. This review examines critical advances in E3 Ub ligase research in plant responses to biotic and abiotic stresses. It highlights how PROTACs can be applied to target proteins involved in plant stress response to mitigate pathogenic agents and environmental adversities.

Funder

China Postdoctoral Science Foundation

National Natural Science Foundation of China

Publisher

Wiley

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