Jasmonic acid enhancement of anthocyanin accumulation is dependent on phytochrome A signaling pathway under far-red light in Arabidopsis

被引:83
|
作者
Li, Ting [1 ,2 ]
Jia, Kun-Peng [1 ,2 ]
Lian, Hong-Li [3 ]
Yang, Xu [4 ]
Li, Ling [3 ]
Yang, Hong-Quan [3 ]
机构
[1] Shanghai Jiao Tong Univ, Minist Agr, Key Lab Urban Agr South, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Agr & Biol Sci, Shanghai 200240, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, Shanghai 200240, Peoples R China
[4] Henan Univ, Sch Life Sci, Kaifeng 475001, Peoples R China
基金
中国国家自然科学基金;
关键词
Anthocyanin; COP1; Far-red light; Jasmonic acid; MYB75; Phytochrome A; TRANSCRIPTION FACTORS; BLUE-LIGHT; GENE-EXPRESSION; COP1; BIOSYNTHESIS; PROTEINS; DOMAIN; CRYPTOCHROMES; ACTIVATION; REPRESSORS;
D O I
10.1016/j.bbrc.2014.10.059
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Anthocyanins are critical for plants. It is shown that the expression of genes encoding the key enzymes such as dihydroflavonol 4-reductase (DFR), UDP-Glc: flavonoid 3-O-glucosyltransferase (UF3GT), and leucoanthocyanidin dioxygenase (LDOX) in anthocyanin biosynthesis pathway is regulated by MYB75, a R2R3 MYB transcription factor. The production of anthocyanin is known to be promoted by jasmonic acid (JA) in light but not in darkness. The photoreceptors cryptochrome 1 (CRY1), phytochrome B (phyB), and phytochrome A (phyA) are also shown to mediate light promotion of anthocyanin accumulation, respectively, whereas their downstream factor COP1, a master negative regulator of photomorphogensis, represses anthocyanin accumulation. However, whether JA coordinates with photoreceptors in the regulation of anthocyanin accumulation is unknown. Here, we show that under far-red light, JA promotes anthocyanin accumulation in a phyA signaling pathway-dependent manner. The phyA mutant is hyposensitive to jasmonic acid analog methyl jasmonic acid (MeJA) under far-red light. The dominant mutant of MYB75, pap1-D, accumulates significantly higher levels of anthocyanin than wild type under far-red light, whereas knockdown of MYBs (MYB75, MYB90, MYB113, and MYB114) through RNAi significantly reduces MeJA promotion of anthocyanin accumulation. The phyA pap1-D double mutant shows reduced responsiveness to MeJA, similar to phyA mutant under far-red light. In darkness, a mutant allele of cop1, cop1-4, shows enhanced responsiveness to MeJA, but pap1-D mutant is barely responsive to MeJA. Upon MeJA application, the cop1-4 pap1-D double mutant accumulates considerably higher levels of anthocyanin than cop1-4 in darkness. Protein studies indicate that MYB75 protein is stabilized by white light and far-red light. Further gene expression studies suggest that MeJA promotes the expression of DFR, UF3GT, and LDOX genes in a phyA- and MYB75-dependent manner under far-red light. Our findings suggest that JA promotion of anthocyanin accumulation under far-red light is dependent on phyA signaling pathway, consisting of phyA, COP1, and MYB75. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:78 / 83
页数:6
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