Related Experiment Video
Updated: Jun 24, 2026

A Flexible Low Cost Hydroponic System for Assessing Plant Responses to Small Molecules in Sterile Conditions
Published on: August 25, 2018
GhIMP10D, an inositol monophosphatase gene enhancing alkaline stress tolerance in plants
Yapeng Fan1, Xuke Lu2, Xiugui Chen2
1Institute of Cotton Research of Chinese Academy of Agricultural Sciences / Zhengzhou Research Base, State Key Laboratory of Cotton Bio-breeding and Integrated Utilization, School of Agricultural Sciences, Zhengzhou University / National Center of Technology Innovation for Comprehensive Utilization of Saline-Alkali Land, Anyang 455000, Henan, China; College of Life Sciences, Shanxi Agricultural University, Taigu, Shanxi 030800, China.
Introduction:
Soil salinization and alkalization are major challenges to global agricultural productivity and food security. Ascorbic acid (AsA) is an essential antioxidant that helps plants mitigate various abiotic stresses. However, the genetic mechanisms underlying AsA's role in enhancing alkaline stress tolerance remain poorly understood.
Objectives:
The objective of this study was to determine whether GhIMP10D, a gene involved in AsA biosynthesis, enhances alkaline stress tolerance in cotton and Arabidopsis by modulating AsA accumulation and cell wall integrity.
Methods:
We performed gene identification and functional analysis using overexpression and silencing techniques in Arabidopsis, rice, and cotton. GhIMP10D, a gene involved in the AsA biosynthesis pathway, was studied for its response to alkaline stress. The role of the bHLH transcription factor GhbHLH48 in regulating GhIMP10D was also explored.
Results:
Our findings showed that overexpression of GhIMP10D resulted in increased AsA production, reduced reactive oxygen species (ROS), and enhanced cell wall integrity in the tested plants. In contrast, silencing GhIMP10D compromised alkaline stress adaptation. We further identified that GhbHLH48 directly activates GhIMP10D by binding to its promoter's G-box element. Manipulating GhbHLH48 levels altered AsA, lignin, and cellulose content, which affected ROS balance and cell wall biosynthesis.
Conclusion:
The GhbHLH48-GhIMP10D regulatory module plays a crucial role in AsA biosynthesis and the maintenance of cell wall integrity under alkaline stress. These findings contribute to a better understanding of AsA signaling pathways and cell wall formation in response to alkaline stress, offering potential strategies for enhancing plant stress tolerance.