Comprehensive metabolome and transcriptome analyses shed light on the regulation of SlNF-YA3b in carotenoid biosynthesis in tomato fruit

IF 6.4 1区 农林科学 Q1 AGRONOMY Postharvest Biology and Technology Pub Date : 2024-10-14 DOI:10.1016/j.postharvbio.2024.113263
Peiwen Wang , Siyu Ran , Yuanhang Xu , Fulei Mo , Fengshuo Li , Rui Lv , Fanyue Meng , Huixin Zhang , Yuxin Zou , Lei Yu , Tianyue Yu , Mozhen Cheng , Yang Liu , Xiuling Chen , Xiaoxuan Zhang , Aoxue Wang
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Abstract

Fruit are an important source of human dietary nutrition, in which carotenoids are crucial for their appearance and nutritional quality. However, the regulatory network of carotenoid biosynthesis in the fruit of horticultural crops remains obscure. Here, a natural tomato mutant, yellowing mutant (ym), in the genetic background of Solanum lycopersicum cultivar ‘Zhongshu 4’ (ZS4) was investigated. Phenotypic analysis showed that the coloring of ym fruit was delayed compared to their wild type, and carotenoid content in ym fruit was significantly lower than that of ZS4 fruit. Integrative metabolome and transcriptome profiling was used to analyze the dynamic changes of carotenoid metabolite content and gene expression in ZS4 and ym fruit during ripening, and differences in carotenoid metabolite content and gene expression between ZS4 and ym fruit were compared. In contrast to ZS4 fruit, the content of carotenes dramatically decreased in ym fruit, of which phytoene and lycopene levels were down-regulated in ym throughout fruit ripening. In the process of fruit ripening, the transcriptome fluctuation of ym was obviously stronger than that of ZS4. Differences in gene expression between ZS4 and ym gradually reduced with fruit ripening. Furthermore, 105 consistently up-regulated and 113 consistently down-regulated genes were found in ym fruit during ripening. KEGG pathway enrichment analyses indicated that differentially expressed genes between ZS4 and ym were implicated in the carotenoid biosynthesis pathway. Correlation analysis showed that 28 genes were positively correlated with phytoene and lycopene content, including SlNF-YA3b (Solyc12G000315) encoding an NF-YA subunit of nuclear factor Y (NF-Y) transcription factors. Expression analysis exhibited that SlNF-YA3b presented a ripening-related expression pattern. Virus-induced gene silencing demonstrated that SlNF-YA3b positively regulated carotenoid accumulation in tomato fruit. Yeast-one hybrid and transcriptional activity assays showed that SlNF-YA3b could bind to the promoter of the carotenogenic gene SlPDS (Solyc03G003570) and promote its transcription. These data suggest that SlNF-YA3b may participate in the regulation of carotenoid biosynthesis in tomato fruit by directly activating the expression of SlPDS. Our findings not only achieve deeper insights into the regulatory mechanisms of carotenoid biosynthesis in the fruit of horticultural crops but also provide better guidance for the improvement of fruit quality maintenance technologies.
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综合代谢组和转录组分析揭示了 SlNF-YA3b 在番茄果实类胡萝卜素生物合成中的调控作用
水果是人类膳食营养的重要来源,其中类胡萝卜素对水果的外观和营养质量至关重要。然而,园艺作物果实中类胡萝卜素生物合成的调控网络仍然模糊不清。本文研究了以番茄栽培品种 "中树 4 号"(ZS4)为遗传背景的天然番茄突变体--黄化突变体(ym)。表型分析表明,与野生型相比,ym果实着色延迟,类胡萝卜素含量明显低于ZS4果实。利用代谢组和转录组综合分析方法分析了ZS4和ym果实成熟过程中类胡萝卜素代谢物含量和基因表达的动态变化,并比较了ZS4和ym果实中类胡萝卜素代谢物含量和基因表达的差异。与 ZS4 果实相比,ym 果实中类胡萝卜素的含量急剧下降,其中植物烯和番茄红素的含量在整个果实成熟过程中均呈下调趋势。在果实成熟过程中,ym 的转录组波动明显强于 ZS4。随着果实成熟,ZS4 和 ym 的基因表达差异逐渐缩小。此外,在 ym 果实成熟过程中,发现 105 个基因持续上调,113 个基因持续下调。KEGG 通路富集分析表明,ZS4 和 ym 的差异表达基因与类胡萝卜素生物合成通路有关。相关性分析表明,28个基因与植物烯和番茄红素含量呈正相关,其中包括编码核因子Y(NF-Y)转录因子NF-YA亚基的SlNF-YA3b(Solyc12G000315)。表达分析表明,SlNF-YA3b呈现出与成熟相关的表达模式。病毒诱导的基因沉默表明,SlNF-YA3b 能正向调节番茄果实中类胡萝卜素的积累。酵母一杂交和转录活性试验表明,SlNF-YA3b能与胡萝卜素生成基因SlPDS(Solyc03G003570)的启动子结合并促进其转录。这些数据表明,SlNF-YA3b可能通过直接激活SlPDS的表达,参与调控番茄果实中类胡萝卜素的生物合成。我们的研究结果不仅加深了对园艺作物果实类胡萝卜素生物合成调控机制的认识,也为果实品质保持技术的改进提供了更好的指导。
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来源期刊
Postharvest Biology and Technology
Postharvest Biology and Technology 农林科学-农艺学
CiteScore
12.00
自引率
11.40%
发文量
309
审稿时长
38 days
期刊介绍: The journal is devoted exclusively to the publication of original papers, review articles and frontiers articles on biological and technological postharvest research. This includes the areas of postharvest storage, treatments and underpinning mechanisms, quality evaluation, packaging, handling and distribution of fresh horticultural crops including fruit, vegetables, flowers and nuts, but excluding grains, seeds and forages. Papers reporting novel insights from fundamental and interdisciplinary research will be particularly encouraged. These disciplines include systems biology, bioinformatics, entomology, plant physiology, plant pathology, (bio)chemistry, engineering, modelling, and technologies for nondestructive testing. Manuscripts on fresh food crops that will be further processed after postharvest storage, or on food processes beyond refrigeration, packaging and minimal processing will not be considered.
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