Characterization of genes involved in pear ascorbic acid metabolism and their response to bagging treatment during 'Yali' fruit development

被引:14
|
作者
Wang, Libin [1 ,2 ]
Ma, Min [1 ]
Zhang, Suling [1 ]
Wu, Zhangfei [1 ]
Li, Jian [3 ]
Luo, Weiqi [4 ]
Guo, Lin [1 ]
Lin, Wei [2 ]
Zhang, Shaoling [1 ]
机构
[1] Nanjing Agr Univ, Ctr Pear Engn Technol Res, State Key Lab Crop Genet & Germplasm Enhancement, Nanjing 210095, Jiangsu, Peoples R China
[2] Nanjing Forestry Univ, Coll Light Ind & Food Engn, Nanjing 210037, Jiangsu, Peoples R China
[3] Beijing Technol & Business Univ, Beijing Adv Innovat Ctr Food Nutr & Human Hlth, Beijing 100048, Peoples R China
[4] ARS, USDA, Hort Res Lab, 2001 S Rock Rd, Ft Pierce, FL 34945 USA
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Pear fruit; Bagging treatment; AsA metabolism; Family gene; Gene profile; ENHANCED TOLERANCE; EXPRESSION; GENOME; OVEREXPRESSION; IDENTIFICATION; BIOSYNTHESIS; FAMILY; SALT;
D O I
10.1016/j.scienta.2021.110178
中图分类号
S6 [园艺];
学科分类号
0902 ;
摘要
In this study, a total of 59 genes involved in ascorbic acid (AsA) metabolism were identified from pear genome with diverse chromosome locations, gene structures, and cis-acting elements. Most were derived from WGD/ segmental duplication blocks, and purifying selection was the main driving force for their expansion. Their expression profiles were tissue-specific, and postharvest light treatment would alter their expression profiles. During 'Yali' pear development, in association with visual and inner quality change, AsA, dehydroascorbate (DHA) and total AsA (T-AsA) concentrations decreased in association with the downregulated activities of glutathione oxidoreductase (GR), L-galactono-1, 4-lactone dehydrogenase (GalLDH), ascorbate peroxidase (APX), monodehydroascorbate reductase (MDHAR), dehydroascorbate reductase (DHAR) and ascorbate oxidase (AO) as well as various expression patterns of 59 genes in their metabolic pathway. Bagging treatment obviously suppressed AsA and T-AsA concentrations in both pericarp and cortex, which accompanied with the downregulated GalLDH, GR, MDHAR, and APX activities and the upregulated AO activity. Furthermore, the expression profiles of several genes in the pericarp and cortex were altered after bagging. In combination of the results from quality, physiological-biochemical and gene expression assay, several genes were proposedly responsible for bagginginduced reduction of AsA and T-AsA concentrations in the pericarp and cortex.
引用
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页数:10
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