Ethylene Responses in Rice Roots and Coleoptiles Are Differentially Regulated by a Carotenoid Isomerase-Mediated Abscisic Acid Pathway
Author(s) -
CuiCui Yin,
Biao Ma,
Derek Collinge,
Barry J. Pogson,
Sijie He,
Qing Xiong,
Kai-Xuan Duan,
Hui Chen,
Chao Yang,
Xiang Lu,
Yiqin Wang,
WanKe Zhang,
Chengcai Chu,
Xiao-Hong Sun,
Shuang Fang,
Jinfang Chu,
Tiegang Lu,
ShouYi Chen,
JinSong Zhang
Publication year - 2015
Publication title -
the plant cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.324
H-Index - 341
eISSN - 1532-298X
pISSN - 1040-4651
DOI - 10.1105/tpc.15.00080
Subject(s) - abscisic acid , ethylene , coleoptile , biology , etiolation , mutant , biochemistry , oryza sativa , plant hormone , arabidopsis , carotenoid , auxin , biosynthesis , neoxanthin , microbiology and biotechnology , gene , enzyme , lutein , zeaxanthin , catalysis
Ethylene and abscisic acid (ABA) act synergistically or antagonistically to regulate plant growth and development. ABA is derived from the carotenoid biosynthesis pathway. Here, we analyzed the interplay among ethylene, carotenoid biogenesis, and ABA in rice (Oryza sativa) using the rice ethylene response mutant mhz5, which displays a reduced ethylene response in roots but an enhanced ethylene response in coleoptiles. We found that MHZ5 encodes a carotenoid isomerase and that the mutation in mhz5 blocks carotenoid biosynthesis, reduces ABA accumulation, and promotes ethylene production in etiolated seedlings. ABA can largely rescue the ethylene response of the mhz5 mutant. Ethylene induces MHZ5 expression, the production of neoxanthin, an ABA biosynthesis precursor, and ABA accumulation in roots. MHZ5 overexpression results in enhanced ethylene sensitivity in roots and reduced ethylene sensitivity in coleoptiles. Mutation or overexpression of MHZ5 also alters the expression of ethylene-responsive genes. Genetic studies revealed that the MHZ5-mediated ABA pathway acts downstream of ethylene signaling to inhibit root growth. The MHZ5-mediated ABA pathway likely acts upstream but negatively regulates ethylene signaling to control coleoptile growth. Our study reveals novel interactions among ethylene, carotenogenesis, and ABA and provides insight into improvements in agronomic traits and adaptive growth through the manipulation of these pathways in rice.
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