Changes in Fruit Firmness, Cell Wall Composition, and Transcriptional Profile in the yellow fruit tomato 1 (yft1) Mutant

被引:19
|
作者
Li, Ling [1 ]
Zhao, Weihua [1 ,2 ]
Feng, Xuechao [1 ]
Chen, Lulu [1 ,2 ]
Zhang, Lida [1 ]
Zhao, Lingxia [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Agr & Biol, Dept Plant Sci, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Agr & Biol, Joint Tomato Res Inst, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
yellow fruit tomato 1 mutant; fruit firmness; softening; cell structure; transcriptomics; primary cell wall; SUCROSE-PHOSPHATE SYNTHASE; TOMATO FRUIT; ACID INVERTASE; SHELF-LIFE; EXPRESSION; GENE; INHIBITION; RIN; LYCOPENE; MUTATION;
D O I
10.1021/acs.jafc.8b04611
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Fruit firmness is an important trait in tomato (Solanum lycopersicum), associated with shelf life and economic value; however, the precise mechanism determining fruit softening remains elusive. A yellow fruit tomato 1 (yft1) mutant harbors a genetic lesion in the YFT1 gene and has significantly firmer fruit than those of the cv. M82 wild type at a red ripe stage, 54 days post-anthesis (dpa). When softening was further dissected, it was found that the yft1 firm fruit phenotype correlated with a difference in cellulose, hemicellulose, and pectin deposition in the primary cell wall (PCW) compared to cv. M82. Alterations in the structure of the pericarp cells, chemical components, hydrolase activities, and expression of genes encoding these hydrolases were all hypothesized to be a result of the loss of YFT1 function. This was further affirmed by RNA-seq analysis, where a total of 183 differentially expressed genes (DEGs, 50/133 down-/upregulated) were identified between yft1 and cv. M82. These DEGs were mainly annotated as participating in ethylene- and auxin-related signal transduction, sugar metabolism, and photosynthesis. This study provides new insights into the mechanism underlying the control of fruit softening.
引用
收藏
页码:463 / 472
页数:10
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