The <i>LpHsfA2</i>‐molecular module confers thermotolerance via fine tuning of its transcription in perennial ryegrass (<i>Lolium perenne</i> L.)

Temperature sensitivity and tolerance play a key role in plant survival and production. Perennial ryegrass (Lolium perenne L.), widely cultivated in cool-season for forage supply and turfgrass, is extremely susceptible to high temperatures, therefore serving as an excellent grass for dissecting the genomic and genetic basis of high-temperature adaptation. In this study, expression analysis revealed that LpHsfA2, an important gene associated with high-temperature tolerance in perennial ryegrass, is rapidly and substantially induced under heat stress. Additionally, heat-tolerant varieties consistently display elevated expression levels of LpHsfA2 compared with heat-sensitive ones. Comparative haplotype analysis of the LpHsfA2 promoter indicated an uneven distribution of two haplotypes (HsfA2<sup>Hap1</sup> and HsfA2<sup>Hap2</sup>) across varieties with differing heat tolerance. Specifically, the HsfA2<sup>Hap1</sup> allele is predominantly present in heat-tolerant varieties, while the HsfA2<sup>Hap2</sup> allele exhibits the opposite pattern. Overexpression of LpHsfA2 confers enhanced thermotolerance, whereas silencing of LpHsfA2 compromises heat tolerance. Furthermore, LpHsfA2 orchestrates its protective effects by directly binding to the promoters of LpHSP18.2 and LpAPX1 to activate their expression, preventing the non-specific misfolding of intracellular protein and the accumulation of reactive oxygen species in cells. Additionally, LpHsfA4 and LpHsfA5 were shown to engage directly with the promoter of LpHsfA2, upregulating its expression as well as the expression of LpHSP18.2 and LpAPX1, thus contributing to enhanced heat tolerance. Markedly, LpHsfA2 possesses autoregulatory ability by directly binding to its own promoter to modulate the self-transcription. Based on these findings, we propose a model for modulating the thermotolerance of perennial ryegrass by precisely regulating the expression of LpHsfA2. Collectively, these findings provide a scientific basis for the development of thermotolerant perennial ryegrass cultivars.

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Publication Details

Journal
Journal of Integrative Plant Biology
Published
2024-10-18
DOI
https://doi.org/10.1111/jipb.13789
Citations
7
Primary Topic
Plant Stress Responses and Tolerance
Type
article
Field-Weighted Citation Impact
4.20

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article

The LpHsfA2‐molecular module confers thermotolerance via fine tuning of its transcription in perennial ryegrass (Lolium perenne L.)

Longxing Hu, Guangjing Ma, Shurui Song, Yan Xie et al.
7 citations
Journal of Integrative Plant Biology
Plant Stress Responses and Tolerance
4.20
article

The LpHsfA2‐molecular module confers thermotolerance via fine tuning of its transcription in perennial ryegrass (Lolium perenne L.)

Longxing Hu, Guangjing Ma, Shurui Song, Yan Xie, Liang Chen, Zhihao Liu, Jing Gao, Liwen Cao, Shilong Cao, Shutsung Liao, Hai‐Chun Jing
article en
7 citations

Abstract

Temperature sensitivity and tolerance play a key role in plant survival and production. Perennial ryegrass (Lolium perenne L.), widely cultivated in cool-season for forage supply and turfgrass, is extremely susceptible to high temperatures, therefore serving as an excellent grass for dissecting the genomic and genetic basis of high-temperature adaptation. In this study, expression analysis revealed that LpHsfA2, an important gene associated with high-temperature tolerance in perennial ryegrass, is rapidly and substantially induced under heat stress. Additionally, heat-tolerant varieties consistently display elevated expression levels of LpHsfA2 compared with heat-sensitive ones. Comparative haplotype analysis of the LpHsfA2 promoter indicated an uneven distribution of two haplotypes (HsfA2<sup>Hap1</sup> and HsfA2<sup>Hap2</sup>) across varieties with differing heat tolerance. Specifically, the HsfA2<sup>Hap1</sup> allele is predominantly present in heat-tolerant varieties, while the HsfA2<sup>Hap2</sup> allele exhibits the opposite pattern. Overexpression of LpHsfA2 confers enhanced thermotolerance, whereas silencing of LpHsfA2 compromises heat tolerance. Furthermore, LpHsfA2 orchestrates its protective effects by directly binding to the promoters of LpHSP18.2 and LpAPX1 to activate their expression, preventing the non-specific misfolding of intracellular protein and the accumulation of reactive oxygen species in cells. Additionally, LpHsfA4 and LpHsfA5 were shown to engage directly with the promoter of LpHsfA2, upregulating its expression as well as the expression of LpHSP18.2 and LpAPX1, thus contributing to enhanced heat tolerance. Markedly, LpHsfA2 possesses autoregulatory ability by directly binding to its own promoter to modulate the self-transcription. Based on these findings, we propose a model for modulating the thermotolerance of perennial ryegrass by precisely regulating the expression of LpHsfA2. Collectively, these findings provide a scientific basis for the development of thermotolerant perennial ryegrass cultivars.

Journal of Integrative Plant BiologyVol. 66(11)
Chinese Academy of Sciences (CN), Beijing Botanical Garden (CN), Wuhan Botanical Garden (CN), Institute of Botany (CN), University of Chinese Academy of Sciences (CN), Hubei Normal University (CN), Hunan Agricultural University (CN)
National Natural Science Foundation of China, Chinese Academy of Sciences, Central China Normal University
Openalex Percentile: Top 6%
Plant Stress Responses and Tolerance
4.20
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