Shafeeq Rahman , Shamma Aldhaheri , Wesam Khader , Jeffin Rockey , Khaled Masmoudi , Nadia Hassan Tawfiq , Abdul Jaleel Cheruth , Wasef Al-Zayadneh , Sonu Krishankumar , Hoor Al Mazmi , Hamda Faisal Al Shehhi , Rashid Abdulla Alzaabi , Shyam Sreedhara Kurup
{"title":"太空飞行破坏了枣椰树种子的转录组动力学和发芽","authors":"Shafeeq Rahman , Shamma Aldhaheri , Wesam Khader , Jeffin Rockey , Khaled Masmoudi , Nadia Hassan Tawfiq , Abdul Jaleel Cheruth , Wasef Al-Zayadneh , Sonu Krishankumar , Hoor Al Mazmi , Hamda Faisal Al Shehhi , Rashid Abdulla Alzaabi , Shyam Sreedhara Kurup","doi":"10.1016/j.stress.2025.101045","DOIUrl":null,"url":null,"abstract":"<div><div>Spaceflight offers a unique setting for investigating plant stress responses and molecular pathways that enable adaptation to microgravity. Here, we examined the physiological and transcriptomic responses of date palm (<em>Phoenix dactylifera</em> L.) seeds maintained aboard the International Space Station (ISS) for six months. Germination assays revealed that space-exposed seeds from six cultivars failed to germinate, even after exogenous gibberellic acid and cytokinin treatments, whereas ground controls achieved 100% germination. Biochemical analyses indicated significant reductions in protein content, α-amylase activity, and proline levels, indicating impaired antioxidant capacity and reduced reserve mobilisation. Transcriptomic profiling of three representative cultivars (Lulu, Majdool, and Meselli) revealed extensive differential expression with Majdool exhibiting the strongest suppression. Downregulated genes were enriched in mitochondrial respiration, antioxidant defense, and auxin and ethylene signalling, whereas abscisic acid-related dormancy genes were upregulated. Additional disruptions included the suppression of DNA repair mechanisms, cytoskeletal organisation, and negative gravitropism regulators. The qRT-PCR validation of the selected genes confirmed these trends. Together, these results indicate that spaceflight seeds remain viable but enter a state of physiological stasis enforced by ABA dominance, impaired energy metabolism, oxidative imbalance, and disrupted growth orientation. To our knowledge, this is the first report on the long-term space exposure of a perennial fruit tree, providing new insights into seed biology under microgravity and highlighting critical challenges for future extraterrestrial agriculture.</div></div>","PeriodicalId":34736,"journal":{"name":"Plant Stress","volume":"18 ","pages":"Article 101045"},"PeriodicalIF":6.8000,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Spaceflight Disrupts Transcriptome Dynamics and Germination in Date Palm (Phoenix dactylifera) Seeds\",\"authors\":\"Shafeeq Rahman , Shamma Aldhaheri , Wesam Khader , Jeffin Rockey , Khaled Masmoudi , Nadia Hassan Tawfiq , Abdul Jaleel Cheruth , Wasef Al-Zayadneh , Sonu Krishankumar , Hoor Al Mazmi , Hamda Faisal Al Shehhi , Rashid Abdulla Alzaabi , Shyam Sreedhara Kurup\",\"doi\":\"10.1016/j.stress.2025.101045\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Spaceflight offers a unique setting for investigating plant stress responses and molecular pathways that enable adaptation to microgravity. Here, we examined the physiological and transcriptomic responses of date palm (<em>Phoenix dactylifera</em> L.) seeds maintained aboard the International Space Station (ISS) for six months. Germination assays revealed that space-exposed seeds from six cultivars failed to germinate, even after exogenous gibberellic acid and cytokinin treatments, whereas ground controls achieved 100% germination. Biochemical analyses indicated significant reductions in protein content, α-amylase activity, and proline levels, indicating impaired antioxidant capacity and reduced reserve mobilisation. Transcriptomic profiling of three representative cultivars (Lulu, Majdool, and Meselli) revealed extensive differential expression with Majdool exhibiting the strongest suppression. Downregulated genes were enriched in mitochondrial respiration, antioxidant defense, and auxin and ethylene signalling, whereas abscisic acid-related dormancy genes were upregulated. Additional disruptions included the suppression of DNA repair mechanisms, cytoskeletal organisation, and negative gravitropism regulators. The qRT-PCR validation of the selected genes confirmed these trends. Together, these results indicate that spaceflight seeds remain viable but enter a state of physiological stasis enforced by ABA dominance, impaired energy metabolism, oxidative imbalance, and disrupted growth orientation. To our knowledge, this is the first report on the long-term space exposure of a perennial fruit tree, providing new insights into seed biology under microgravity and highlighting critical challenges for future extraterrestrial agriculture.</div></div>\",\"PeriodicalId\":34736,\"journal\":{\"name\":\"Plant Stress\",\"volume\":\"18 \",\"pages\":\"Article 101045\"},\"PeriodicalIF\":6.8000,\"publicationDate\":\"2025-09-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Stress\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2667064X25003136\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Stress","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667064X25003136","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
Spaceflight Disrupts Transcriptome Dynamics and Germination in Date Palm (Phoenix dactylifera) Seeds
Spaceflight offers a unique setting for investigating plant stress responses and molecular pathways that enable adaptation to microgravity. Here, we examined the physiological and transcriptomic responses of date palm (Phoenix dactylifera L.) seeds maintained aboard the International Space Station (ISS) for six months. Germination assays revealed that space-exposed seeds from six cultivars failed to germinate, even after exogenous gibberellic acid and cytokinin treatments, whereas ground controls achieved 100% germination. Biochemical analyses indicated significant reductions in protein content, α-amylase activity, and proline levels, indicating impaired antioxidant capacity and reduced reserve mobilisation. Transcriptomic profiling of three representative cultivars (Lulu, Majdool, and Meselli) revealed extensive differential expression with Majdool exhibiting the strongest suppression. Downregulated genes were enriched in mitochondrial respiration, antioxidant defense, and auxin and ethylene signalling, whereas abscisic acid-related dormancy genes were upregulated. Additional disruptions included the suppression of DNA repair mechanisms, cytoskeletal organisation, and negative gravitropism regulators. The qRT-PCR validation of the selected genes confirmed these trends. Together, these results indicate that spaceflight seeds remain viable but enter a state of physiological stasis enforced by ABA dominance, impaired energy metabolism, oxidative imbalance, and disrupted growth orientation. To our knowledge, this is the first report on the long-term space exposure of a perennial fruit tree, providing new insights into seed biology under microgravity and highlighting critical challenges for future extraterrestrial agriculture.
期刊介绍:
The journal Plant Stress deals with plant (or other photoautotrophs, such as algae, cyanobacteria and lichens) responses to abiotic and biotic stress factors that can result in limited growth and productivity. Such responses can be analyzed and described at a physiological, biochemical and molecular level. Experimental approaches/technologies aiming to improve growth and productivity with a potential for downstream validation under stress conditions will also be considered. Both fundamental and applied research manuscripts are welcome, provided that clear mechanistic hypotheses are made and descriptive approaches are avoided. In addition, high-quality review articles will also be considered, provided they follow a critical approach and stimulate thought for future research avenues.
Plant Stress welcomes high-quality manuscripts related (but not limited) to interactions between plants and:
Lack of water (drought) and excess (flooding),
Salinity stress,
Elevated temperature and/or low temperature (chilling and freezing),
Hypoxia and/or anoxia,
Mineral nutrient excess and/or deficiency,
Heavy metals and/or metalloids,
Plant priming (chemical, biological, physiological, nanomaterial, biostimulant) approaches for improved stress protection,
Viral, phytoplasma, bacterial and fungal plant-pathogen interactions.
The journal welcomes basic and applied research articles, as well as review articles and short communications. All submitted manuscripts will be subject to a thorough peer-reviewing process.