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综合转录组学和代谢组学分析揭示了患有鳞茎腐烂病的变种动态变化的分子特征。

Integrated transcriptomic and metabolomic analysis reveals the molecular profiles of dynamic variation in var. suffering from bulb rot.

作者信息

Chang Nana, Zheng Lingling, Xu Yang, Wang Chu, Li Hui, Wang Ye

机构信息

Jiangxi Province Key Laboratory of Sustainable Utilization of Traditional Chinese Medicine Resources, Institute of Traditional Chinese Medicine Health Industry, China Academy of Chinese Medical Sciences, Nanchang, China.

Jiangxi Health Industry Institute of Traditional Chinese Medicine, Nanchang, China.

出版信息

Front Genet. 2024 Aug 14;15:1432997. doi: 10.3389/fgene.2024.1432997. eCollection 2024.

DOI:10.3389/fgene.2024.1432997
PMID:39205945
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11349735/
Abstract

var. , known as Longya lily, is a well-known medicinal and edible plant in China. Bulb rot is a common disease in Longya lily cultivation that severely affects the yield and quality of lilies. According field investigations, we found that different Longya lily plants in the same field had different degrees of resistance to root rot. To find the reasons leading to the difference, we performed metabolomic and transcriptomic analyses of Longya lily with different degrees of disease. The transcriptomic analyses showed that the number of differentially expressed genes increased in early and mid-stage infections (LYBH2 and LYBH3), while decreased in late-stage infection (LYBH4). A total of 2309 DEGs showed the same expression trend in diseased bulb compared healthy bulb (LYBH1). The transcription factors (TFs) analysis of DEGs showed that several common TFs, like WRKY, bHLH, AP2/ERF-ERF and MYB, were significantly activated in bulbs after decay. The metabolomic analyses showed that there were 794 differentially accumulated metabolites, and metabolites with significant changes in relative content largely were phenolic acids, followed by flavonoids and amino acids and derivatives. The combined analysis of transcriptome and metabolome indicated that phenylpropanoid biosynthesis pathway was crucial in Longya lily resistance to bulb rot. Therefore, we speculated that the different degree of resistance to bulb rot in Longya lily may be related to the transcript levels of gene and contents of metabolites in the phenylpropanoid biosynthesis pathway. Overall, these results elucidate the molecular responses of Longya lily to bulb rot and lay a theoretical foundation for breeding resistant varieties.

摘要

变种,即龙牙百合,是中国一种著名的药食两用植物。鳞茎腐烂病是龙牙百合种植中的常见病害,严重影响百合的产量和品质。通过田间调查,我们发现同一田块中不同的龙牙百合植株对根腐病的抗性程度不同。为找出导致这种差异的原因,我们对不同病害程度的龙牙百合进行了代谢组学和转录组学分析。转录组分析表明,在感染早期和中期(LYBH2和LYBH3)差异表达基因的数量增加,而在感染后期(LYBH4)减少。与健康鳞茎(LYBH1)相比,共有2309个差异表达基因在患病鳞茎中呈现相同的表达趋势。对差异表达基因的转录因子(TFs)分析表明,几种常见的转录因子,如WRKY、bHLH、AP2/ERF-ERF和MYB,在鳞茎腐烂后显著激活。代谢组分析表明,有794种差异积累的代谢物,相对含量有显著变化的代谢物主要是酚酸,其次是黄酮类化合物、氨基酸及其衍生物。转录组和代谢组的联合分析表明,苯丙烷生物合成途径在龙牙百合对鳞茎腐烂的抗性中至关重要。因此,我们推测龙牙百合对鳞茎腐烂的不同抗性程度可能与苯丙烷生物合成途径中基因的转录水平和代谢物含量有关。总体而言,这些结果阐明了龙牙百合对鳞茎腐烂的分子反应,为培育抗病品种奠定了理论基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/decc/11349735/0c49834b51ed/fgene-15-1432997-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/decc/11349735/e613639e2ad6/fgene-15-1432997-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/decc/11349735/9e9b91e73f6b/fgene-15-1432997-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/decc/11349735/15c12e8fff82/fgene-15-1432997-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/decc/11349735/291ebd70808c/fgene-15-1432997-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/decc/11349735/0e443bb2230f/fgene-15-1432997-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/decc/11349735/3e3b8335c6ef/fgene-15-1432997-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/decc/11349735/fec1d9cba624/fgene-15-1432997-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/decc/11349735/0c49834b51ed/fgene-15-1432997-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/decc/11349735/e613639e2ad6/fgene-15-1432997-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/decc/11349735/9e9b91e73f6b/fgene-15-1432997-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/decc/11349735/15c12e8fff82/fgene-15-1432997-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/decc/11349735/291ebd70808c/fgene-15-1432997-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/decc/11349735/0e443bb2230f/fgene-15-1432997-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/decc/11349735/3e3b8335c6ef/fgene-15-1432997-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/decc/11349735/fec1d9cba624/fgene-15-1432997-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/decc/11349735/0c49834b51ed/fgene-15-1432997-g008.jpg

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