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Comparative proteomics in tall fescue to reveal underlying mechanisms for improving Photosystem II thermotolerance during heat stress memory.
Wang, Guangyang; Wang, Xiulei; Li, Dongli; Yang, Xuehe; Hu, Tao; Fu, Jinmin.
Affiliation
  • Wang G; School of Resources and Environmental Engineering, Ludong University, Yantai City, 264025, China.
  • Wang X; Urban Management Bureau, Taiqian County, Puyang City, 457600, China.
  • Li D; School of Resources and Environmental Engineering, Ludong University, Yantai City, 264025, China.
  • Yang X; School of Resources and Environmental Engineering, Ludong University, Yantai City, 264025, China.
  • Hu T; State Key Laboratory of Herbage Improvement and Grassland Agro-ecosystems, College of Pastoral Agriculture Science and Technology, Lanzhou University, Lanzhou city, 730020, China. hut@lzu.edu.cn.
  • Fu J; School of Resources and Environmental Engineering, Ludong University, Yantai City, 264025, China. 1162933849@qq.com.
BMC Genomics ; 25(1): 683, 2024 Jul 09.
Article de En | MEDLINE | ID: mdl-38982385
ABSTRACT

BACKGROUND:

The escalating impacts of global warming intensify the detrimental effects of heat stress on crop growth and yield. Among the earliest and most vulnerable sites of damage is Photosystem II (PSII). Plants exposed to recurring high temperatures develop heat stress memory, a phenomenon that enables them to retain information from previous stress events to better cope with subsequent one. Understanding the components and regulatory networks associated with heat stress memory is crucial for the development of heat-resistant crops.

RESULTS:

Physiological assays revealed that heat priming (HP) enabled tall fescue to possess higher Photosystem II photochemical activity when subjected to trigger stress. To investigate the underlying mechanisms of heat stress memory, we performed comparative proteomic analyses on tall fescue leaves at S0 (control), R4 (primed), and S5 (triggering), using an integrated approach of Tandem Mass Tag (TMT) labeling and Liquid Chromatography-Mass Spectrometry. A total of 3,851 proteins were detected, with quantitative information available for 3,835 proteins. Among these, we identified 1,423 differentially abundant proteins (DAPs), including 526 proteins that were classified as Heat Stress Memory Proteins (HSMPs). GO and KEGG enrichment analyses revealed that the HSMPs were primarily associated with the "autophagy" in R4 and with "PSII repair", "HSP binding", and "peptidase activity" in S5. Notably, we identified 7 chloroplast-localized HSMPs (HSP21, DJC77, EGY3, LHCA4, LQY1, PSBR and DEGP8, R4/S0 > 1.2, S5/S0 > 1.2), which were considered to be effectors linked to PSII heat stress memory, predominantly in cluster 4. Protein-protein interaction (PPI) analysis indicated that the ubiquitin-proteasome system, with key nodes at UPL3, RAD23b, and UCH3, might play a role in the selective retention of memory effectors in the R4 stage. Furthermore, we conducted RT-qPCR validation on 12 genes, and the results showed that in comparison to the S5 stage, the R4 stage exhibited reduced consistency between transcript and protein levels, providing additional evidence for post-transcriptional regulation in R4.

CONCLUSIONS:

These findings provide valuable insights into the establishment of heat stress memory under recurring high-temperature episodes and offer a conceptual framework for breeding thermotolerant crops with improved PSII functionality.
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Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Réaction de choc thermique / Protéomique / Complexe protéique du photosystème II / Thermotolérance Langue: En Journal: BMC Genomics Sujet du journal: GENETICA Année: 2024 Type de document: Article Pays d'affiliation: Chine Pays de publication: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Réaction de choc thermique / Protéomique / Complexe protéique du photosystème II / Thermotolérance Langue: En Journal: BMC Genomics Sujet du journal: GENETICA Année: 2024 Type de document: Article Pays d'affiliation: Chine Pays de publication: Royaume-Uni