Exogenous Melatonin Effects on Drought-Stressed Longan Plants: Physiology and Transcriptome Insights

IF 4.1 2区 农林科学 Q1 AGRONOMY
Beibei Qi, Rongshao Huang, Qin XianQuan, Ning Xu, Liangbo Li, Kexin Cao, Hongye Qiu, Jianhua Chen
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引用次数: 0

Abstract

Drought stress severely constrains yield and quality stability in longan (Dimocarpus longan Lour.), an important medicine and food homology fruit in China. Melatonin (MT) shows potential for alleviating abiotic stress, but its mechanisms in drought-stressed longan remain unclear. Here, we investigated two cultivars (Shixia and Chuliang) under drought and exogenous MT treatments (CW, well-watered control; CM, exogenous MT application under well-watered control; DW, drought stress; DM, exogenous MT application under drought stress), revealing the following findings: (i) Drought treatment significantly reduced endogenous MT levels in both studied cultivars, and the reduction was reversed by exogenous foliar MT application. Specifically, under drought conditions, exogenous MT treatment increased endogenous MT content by 272.7% in Shixia and 53.6% in Chuliang, respectively. (ii) Drought and exogenous MT treatments modulated the activities of plant defense enzymes (superoxide dismutase, SOD; peroxidase, POD; phenylalanine ammonia lyase, PAL; and catalase, CAT) and the levels of related metabolites (malondialdehyde, MDA; proline, Pro). Across both cultivars, drought stress increased the activities of SOD, POD, and PAL, as well as the Pro content. Exogenous MT treatment, however, reduced the activities of SOD, POD, and PAL while increasing CAT activity and MDA content to some extent in both cultivars. Notably, the Pro content was significantly reduced in Shixia but significantly increased in Chuliang following exogenous MT application under drought stress. (iii) Drought and exogenous MT treatments regulated gene expression in longan cultivars. Relative to CW, 848, 3356, and 2447 differentially expressed genes (DEGs) were detected in CM, DW, and DM in Shixia, respectively. Relative to CW, 1349, 5260, and 5116 DEGs were identified in CM, DW, and DM in Chuliang. A gene ontology analysis indicated significant enrichment for abiotic stress defense and hormone-responsive processes. The KEGG pathway analysis showed significant enrichment in protein processing in the endoplasmic reticulum (ko04141), amino sugar and nucleotide sugar metabolism (ko00520), ascorbate and aldarate metabolism (ko00053), plant–pathogen interaction (ko04626), and starch and sucrose metabolism (ko00500). These findings provide physiological and transcriptomic insights into MT-regulated drought responses in longan, highlighting its potential for improving productivity in drought-prone regions.
外源褪黑素对干旱胁迫龙眼植物的影响:生理和转录组研究
龙眼是中国重要的药食同源水果,干旱胁迫严重制约了其产量和品质稳定性。褪黑素(Melatonin, MT)显示出缓解非生物胁迫的潜力,但其在干旱胁迫龙眼中的作用机制尚不清楚。在干旱和外源MT处理(CW,水分充足对照;CM,水分充足对照下的外源MT处理;DW,干旱胁迫下的外源MT处理;DM,干旱胁迫下的外源MT处理)下,研究发现:(i)干旱处理显著降低了两个研究品种的内源MT水平,外源叶面MT处理逆转了这种降低。其中,在干旱条件下,外源MT处理使石夏和楚梁的内源MT含量分别提高了272.7%和53.6%。(ii)干旱和外源MT处理调节了植物防御酶(超氧化物歧化酶,SOD,过氧化物酶,POD,苯丙氨酸解氨酶,PAL和过氧化氢酶,CAT)的活性和相关代谢物(丙二醛,MDA,脯氨酸,Pro)的水平。干旱胁迫使两个品种的SOD、POD和PAL活性增加,Pro含量增加。外源MT处理在一定程度上降低了两个品种的SOD、POD和PAL活性,提高了CAT活性和MDA含量。在干旱胁迫下,外源MT处理后,石夏植株Pro含量显著降低,褚凉植株Pro含量显著升高。(3)干旱和外源MT处理调控龙眼品种基因表达。石峡地区CM、DW和DM分别检测到848、3356和2447个差异表达基因(deg)。相对于CW,楚梁CM、DW和DM分别鉴定出1349、5260和5116个deg。基因本体分析表明,非生物应激防御和激素反应过程显著富集。KEGG通路分析显示,在内质网蛋白质加工(ko04141)、氨基糖和核苷酸糖代谢(ko00520)、抗坏血酸和醛酸盐代谢(ko00053)、植物与病原体相互作用(ko04626)以及淀粉和蔗糖代谢(ko00500)中显著富集。这些发现为mt调控的龙眼干旱响应提供了生理和转录组学方面的见解,突出了其在干旱易发地区提高生产力的潜力。
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来源期刊
Agronomy-Basel
Agronomy-Basel Agricultural and Biological Sciences-Agronomy and Crop Science
CiteScore
6.20
自引率
13.50%
发文量
2665
审稿时长
20.32 days
期刊介绍: Agronomy (ISSN 2073-4395) is an international and cross-disciplinary scholarly journal on agronomy and agroecology. It publishes reviews, regular research papers, communications and short notes, and there is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodical details must be provided for research articles.
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2100 Bioanalyzer
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HiSeq X Ten/NovaSeq 6000 platform
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random hexamer primers
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TruSeq RNA Sample Preparation Kit
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X Ten/NovaSeq 6000 platform
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SuperScript cDNA synthesis kit
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TRIzol Reagent
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Phusion DNA polymerase
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WondaCract ODS-2 C18 column
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Tween 20
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methanol
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DNase I
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NanoDrop ND-2000 spectrophotometer
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melatonin
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