scholarly journals The regulatory mechanism of fruit ripening revealed by analyses of direct targets of the tomato MADS-box transcription factor RIPENING INHIBITOR

2013 ◽  
Vol 8 (6) ◽  
pp. e24357 ◽  
Author(s):  
Masaki Fujisawa ◽  
Yasuhiro Ito
2016 ◽  
Vol 7 ◽  
Author(s):  
Mohammad Irfan ◽  
Sumit Ghosh ◽  
Vijaykumar S. Meli ◽  
Anil Kumar ◽  
Vinay Kumar ◽  
...  

2011 ◽  
Vol 70 (2) ◽  
pp. 243-255 ◽  
Author(s):  
Guozheng Qin ◽  
Yuying Wang ◽  
Baohua Cao ◽  
Weihao Wang ◽  
Shiping Tian

2018 ◽  
Vol 227 ◽  
pp. 124-131 ◽  
Author(s):  
Wenjing Lu ◽  
Jingxin Chen ◽  
Xingchen Ren ◽  
Jiajia Yuan ◽  
Xueyuan Han ◽  
...  

2019 ◽  
Vol 71 (4) ◽  
pp. 1585-1597 ◽  
Author(s):  
Qingjie Wang ◽  
Gongxun Xu ◽  
Xuehui Zhao ◽  
Zejie Zhang ◽  
Xuxu Wang ◽  
...  

Abstract The dormancy-associated MADS-box (DAM) genes PpDAM5 and PpDAM6 have been shown to play important roles in bud endodormancy; however, their molecular regulatory mechanism in peach is unclear. In this study, by use of yeast one-hybrid screening, we isolated a TEOSINTE BRANCHED1/CYCLOIDEA/PROLIFERATING CELL FACTOR transcription factor, PpTCP20, in the peach cultivar ‘Zhongyou 4’ (Prunus persica var. nectarina). The protein was localized in the nucleus and was capable of forming a homodimer. Electrophoretic mobility shift assays demonstrated that PpTCP20 binds to a GCCCR element in the promoters of PpDAM5 and PpDAM6, and transient dual luciferase experiments showed that PpTCP20 inhibited the expression of PpDAM5 and PpDAM6 as the period of the release of flower bud endodormancy approached. In addition, PpTCP20 interacted with PpABF2 to form heterodimers to regulate bud endodormancy, and the content of abscisic acid decreased with the release of endodormancy. PpTCP20 also inhibited expression of PpABF2 to regulate endodormancy. Taken together, our results suggest that PpTCP20 regulates peach flower bud endodormancy by negatively regulating the expression of PpDAM5 and PpDAM6, and by interacting with PpABF2, thus revealing a novel regulatory mechanism in a perennial deciduous tree.


Plant Science ◽  
2020 ◽  
Vol 301 ◽  
pp. 110634
Author(s):  
Xiliang Qi ◽  
Congli Liu ◽  
Lulu Song ◽  
Ming Li

PLoS ONE ◽  
2021 ◽  
Vol 16 (4) ◽  
pp. e0249575
Author(s):  
Yasuhiro Ito ◽  
Nobutaka Nakamura ◽  
Eiichi Kotake-Nara

The tomato (Solanum lycopersicum) ripening inhibitor (rin) mutation completely represses fruit ripening, as rin fruits fail to express ripening-associated genes and remain green and firm. Moreover, heterozygous rin fruits (rin/+) ripen normally but have extended shelf life, an important consideration for this perishable fruit crop; therefore, heterozygous rin has been widely used to breed varieties that produce red tomatoes with improved shelf life. We previously used CRISPR/Cas9 to produce novel alleles at the rin locus. The wild-type allele RIN encodes a MADS-box transcription factor and the novel allele, named as rinG2, generates an early stop codon, resulting in C-terminal truncation of the transcription factor. Like rin fruits, rinG2 fruits exhibit extended shelf life, but unlike rin fruits, which remain yellow-green even after long-term storage, rinG2 fruits turn orange due to ripening-associated carotenoid production. Here, to explore the potential of the rinG2 mutation for breeding, we characterized the effects of rinG2 in the heterozygous state (rinG2/+) compared to the effects of rin/+. The softening of rinG2/+ fruits was delayed compared to the wild type but to a lesser degree than rin/+ fruits. Lycopene and β-carotene levels in rinG2/+ fruits were similar to those of the wild type, whereas rin/+ fruits accumulated half the amount of β-carotene compared to the wild type. The rinG2/+ fruits produced lower levels of ethylene than wild-type and rin/+ fruits. Expression analysis revealed that in rinG2/+ fruits, the rinG2 mutation (like rin) partially inhibited the expression of ripening-associated genes. The small differences in the inhibitory effects of rinG2 vs. rin coincided with small differences in phenotypes, such as ethylene production, softening, and carotenoid accumulation. Therefore, rinG2 represents a promising genetic resource for developing tomato cultivars with extended shelf life.


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