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代谢组学和转录组学分析揭示了自嫁接和异源嫁接对葡萄花青素生物合成的影响。

Metabolomic and transcriptomic analyses reveal the effects of self- and hetero-grafting on anthocyanin biosynthesis in grapevine.

作者信息

Zhong Haixia, Liu Zhongjie, Zhang Fuchun, Zhou Xiaoming, Sun Xiaoxia, Li Yongyao, Liu Wenwen, Xiao Hua, Wang Nan, Lu Hong, Pan Mingqi, Wu Xinyu, Zhou Yongfeng

机构信息

Institute of Horticulture Crops, Xinjiang Academy of Agricultural Sciences (Key Laboratory of Genome Research and Genetic Improvement of Xinjiang Characteristic Fruits and Vegetables), Urumqi, China.

Shenzhen Branch, Guangdong Laboratory of Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture and Rural Affairs, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, China.

出版信息

Hortic Res. 2022 May 17;9:uhac103. doi: 10.1093/hr/uhac103. eCollection 2022.

DOI:10.1093/hr/uhac103
PMID:35795384
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9251602/
Abstract

Grafting, which joins a scion from a cultivar with the stem of a rootstock from a grapevine wild relative, is commonly used in viticulture. Grafting has crucial effects on various phenotypes of the cultivar, including its phenology, biotic and abiotic resistance, berry metabolome, and coloration, but the underlying genetics and regulatory mechanisms are largely unexplored. In this study, we investigated the phenotypic, metabolomic, and transcriptomic profiles at three developmental stages (45, 75, and 105 days after flowering) of the Crimson Seedless cultivar () grafted onto four rootstocks (three heterografts, CS/101-14, CS/SO4, and CS/110R and one self-graft, CS/CS) with own-rooted graft-free Crimson Seedless (CS) as the control. All the heterografts had a significant effect on berry reddening as early as ~45 days after flowering. The grafting of rootstocks promoted anthocyanin biosynthesis and accumulation in grape berries. The metabolomic features showed that cyanidin 3-O-glucoside, delphinidin 3-O-glucoside, malvidin 3-O-glucoside, peonidin 3-O-glucoside, and petunidin 3-O-glucoside were the pigments responsible for the purplish-red peel color. Transcriptomic analyses revealed that anthocyanin biosynthesis-related genes, from upstream (phenylalanine ammonia-lyase) to downstream (anthocyanidin 3-O-glucosyltransferase and anthocyanidin synthase), were upregulated with the accumulation of anthocyanins in the heterografted plants. At the same time, all these genes were also highly expressed and more anthocyanin was accumulated in self-grafted CS/CS samples compared with own-rooted graft-free CS samples, suggesting that self-grafting may also have promoted berry reddening in grapevine. Our results reveal global transcriptomic and metabolomic features in berry color regulation under different grafting conditions that may be useful for improving berry quality in viticulture.

摘要

嫁接是将栽培品种的接穗与葡萄野生近缘种的砧木茎干连接起来,常用于葡萄栽培。嫁接对栽培品种的各种表型有重要影响,包括物候期、生物和非生物抗性、浆果代谢组以及着色,但潜在的遗传学和调控机制在很大程度上尚未得到探索。在本研究中,我们以自根无嫁接的绯红无核(CS)为对照,研究了嫁接在四种砧木(三种异源嫁接,CS/101-14、CS/SO4和CS/110R,一种自嫁接,CS/CS)上的绯红无核品种在三个发育阶段(开花后45、75和105天)的表型、代谢组和转录组特征。所有异源嫁接早在开花后约45天就对浆果变红有显著影响。砧木嫁接促进了葡萄浆果中花青素的生物合成和积累。代谢组学特征表明,矢车菊素3-O-葡萄糖苷、飞燕草素3-O-葡萄糖苷、锦葵素3-O-葡萄糖苷、芍药素3-O-葡萄糖苷和矮牵牛素3-O-葡萄糖苷是导致紫红色果皮颜色的色素。转录组分析表明,在异源嫁接植物中,从上游(苯丙氨酸解氨酶)到下游(花青素3-O-葡萄糖基转移酶和花青素合酶)的花青素生物合成相关基因随着花青素的积累而上调。同时,与自根无嫁接的CS样品相比,所有这些基因在自嫁接的CS/CS样品中也高度表达,并且积累了更多的花青素,这表明自嫁接也可能促进了葡萄的浆果变红。我们的结果揭示了不同嫁接条件下浆果颜色调控中的全局转录组和代谢组特征,这可能有助于提高葡萄栽培中的浆果品质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ca/9251602/e53d9a882d84/uhac103f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ca/9251602/e5a831addc86/uhac103f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ca/9251602/1e9f011b514a/uhac103f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ca/9251602/cd6dd76a57ac/uhac103f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ca/9251602/0135d9404c5e/uhac103f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ca/9251602/788ce81b1dda/uhac103f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ca/9251602/e53d9a882d84/uhac103f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ca/9251602/e5a831addc86/uhac103f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ca/9251602/1e9f011b514a/uhac103f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ca/9251602/cd6dd76a57ac/uhac103f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ca/9251602/0135d9404c5e/uhac103f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ca/9251602/788ce81b1dda/uhac103f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ca/9251602/e53d9a882d84/uhac103f6.jpg

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