Yingying Wu, Jinfeng Liu, Xinyuan Sheng, Wenqiu Wang, Tianchi Wang, Marcela Martinez-Sanchez, Songhu Wang, Meiyan Tu, Jiahui Deng, Andrew C Allan, Ross G Atkinson, Niels J Nieuwenhuizen, Xueren Yin, Yunliu Zeng
{"title":"猕猴桃叶绿素降解的空间调控:AcNAC2-AcSGR1/2级联介导内果皮快速去绿","authors":"Yingying Wu, Jinfeng Liu, Xinyuan Sheng, Wenqiu Wang, Tianchi Wang, Marcela Martinez-Sanchez, Songhu Wang, Meiyan Tu, Jiahui Deng, Andrew C Allan, Ross G Atkinson, Niels J Nieuwenhuizen, Xueren Yin, Yunliu Zeng","doi":"10.1111/pbi.70071","DOIUrl":null,"url":null,"abstract":"<p><p>Changes in skin colour, as a visual cue for fruit ripeness, are important physiological markers in many crops including tomato, banana and grape. In kiwifruit, the skin remains brown during ripening, but de-greening of the pericarp occurs to reveal accumulated carotenoids and anthocyanins in gold- and red-fleshed cultivars. In this study, analysis of the inner and outer pericarp of Actinidia chinensis 'Hongyang' revealed faster chlorophyll degradation in the inner pericarp, compared with the outer pericarp. Based on transcriptome analysis, two chlorophyll degradation-related genes encoding Mg-dechelatases (AcSGR1 and AcSGR2) were more abundantly expressed in the inner pericarp, and this correlated with higher Mg-dechelatase enzyme activity in the inner pericarp than in the outer pericarp. Weighted gene co-expression network analysis identified potential regulators of AcSGR1/2. A differentially expressed NAM/ATAF/CUC transcription factor AcNAC2 was identified, which could directly interact with AcSGR1 and AcSGR2 promoters and strongly activate their expression. A closely related NAC, AcNAC3, also enhanced AcSGR1/2 expression, but was less abundantly expressed. Transient expression in tobacco confirmed that AcNAC2 and AcNAC3 promote chlorophyll degradation, and stable overexpression in kiwifruit verified that AcNAC2 acts via up-regulation of AcSGR1/2 gene expression. CRISPR-mediated knockouts of AcNAC2/3 in kiwifruit dramatically reduced expression levels of AcSGR1/2 genes in fruit, leading to significantly delayed chlorophyll degradation and de-greening. Together, these results suggest that differential chlorophyll degradation drives the differences observed in chlorophyll content between the inner and outer pericarp of kiwifruit, which is principally modulated by the transcription factor AcNAC2.</p>","PeriodicalId":221,"journal":{"name":"Plant Biotechnology Journal","volume":" ","pages":""},"PeriodicalIF":10.1000,"publicationDate":"2025-04-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Spatial regulation of chlorophyll degradation in kiwifruit: AcNAC2-AcSGR1/2 cascades mediate rapid de-greening in the inner pericarp.\",\"authors\":\"Yingying Wu, Jinfeng Liu, Xinyuan Sheng, Wenqiu Wang, Tianchi Wang, Marcela Martinez-Sanchez, Songhu Wang, Meiyan Tu, Jiahui Deng, Andrew C Allan, Ross G Atkinson, Niels J Nieuwenhuizen, Xueren Yin, Yunliu Zeng\",\"doi\":\"10.1111/pbi.70071\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Changes in skin colour, as a visual cue for fruit ripeness, are important physiological markers in many crops including tomato, banana and grape. In kiwifruit, the skin remains brown during ripening, but de-greening of the pericarp occurs to reveal accumulated carotenoids and anthocyanins in gold- and red-fleshed cultivars. In this study, analysis of the inner and outer pericarp of Actinidia chinensis 'Hongyang' revealed faster chlorophyll degradation in the inner pericarp, compared with the outer pericarp. Based on transcriptome analysis, two chlorophyll degradation-related genes encoding Mg-dechelatases (AcSGR1 and AcSGR2) were more abundantly expressed in the inner pericarp, and this correlated with higher Mg-dechelatase enzyme activity in the inner pericarp than in the outer pericarp. Weighted gene co-expression network analysis identified potential regulators of AcSGR1/2. A differentially expressed NAM/ATAF/CUC transcription factor AcNAC2 was identified, which could directly interact with AcSGR1 and AcSGR2 promoters and strongly activate their expression. A closely related NAC, AcNAC3, also enhanced AcSGR1/2 expression, but was less abundantly expressed. Transient expression in tobacco confirmed that AcNAC2 and AcNAC3 promote chlorophyll degradation, and stable overexpression in kiwifruit verified that AcNAC2 acts via up-regulation of AcSGR1/2 gene expression. CRISPR-mediated knockouts of AcNAC2/3 in kiwifruit dramatically reduced expression levels of AcSGR1/2 genes in fruit, leading to significantly delayed chlorophyll degradation and de-greening. Together, these results suggest that differential chlorophyll degradation drives the differences observed in chlorophyll content between the inner and outer pericarp of kiwifruit, which is principally modulated by the transcription factor AcNAC2.</p>\",\"PeriodicalId\":221,\"journal\":{\"name\":\"Plant Biotechnology Journal\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":10.1000,\"publicationDate\":\"2025-04-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Biotechnology Journal\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.1111/pbi.70071\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Biotechnology Journal","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1111/pbi.70071","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
Spatial regulation of chlorophyll degradation in kiwifruit: AcNAC2-AcSGR1/2 cascades mediate rapid de-greening in the inner pericarp.
Changes in skin colour, as a visual cue for fruit ripeness, are important physiological markers in many crops including tomato, banana and grape. In kiwifruit, the skin remains brown during ripening, but de-greening of the pericarp occurs to reveal accumulated carotenoids and anthocyanins in gold- and red-fleshed cultivars. In this study, analysis of the inner and outer pericarp of Actinidia chinensis 'Hongyang' revealed faster chlorophyll degradation in the inner pericarp, compared with the outer pericarp. Based on transcriptome analysis, two chlorophyll degradation-related genes encoding Mg-dechelatases (AcSGR1 and AcSGR2) were more abundantly expressed in the inner pericarp, and this correlated with higher Mg-dechelatase enzyme activity in the inner pericarp than in the outer pericarp. Weighted gene co-expression network analysis identified potential regulators of AcSGR1/2. A differentially expressed NAM/ATAF/CUC transcription factor AcNAC2 was identified, which could directly interact with AcSGR1 and AcSGR2 promoters and strongly activate their expression. A closely related NAC, AcNAC3, also enhanced AcSGR1/2 expression, but was less abundantly expressed. Transient expression in tobacco confirmed that AcNAC2 and AcNAC3 promote chlorophyll degradation, and stable overexpression in kiwifruit verified that AcNAC2 acts via up-regulation of AcSGR1/2 gene expression. CRISPR-mediated knockouts of AcNAC2/3 in kiwifruit dramatically reduced expression levels of AcSGR1/2 genes in fruit, leading to significantly delayed chlorophyll degradation and de-greening. Together, these results suggest that differential chlorophyll degradation drives the differences observed in chlorophyll content between the inner and outer pericarp of kiwifruit, which is principally modulated by the transcription factor AcNAC2.
期刊介绍:
Plant Biotechnology Journal aspires to publish original research and insightful reviews of high impact, authored by prominent researchers in applied plant science. The journal places a special emphasis on molecular plant sciences and their practical applications through plant biotechnology. Our goal is to establish a platform for showcasing significant advances in the field, encompassing curiosity-driven studies with potential applications, strategic research in plant biotechnology, scientific analysis of crucial issues for the beneficial utilization of plant sciences, and assessments of the performance of plant biotechnology products in practical applications.