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Promotion of BR Biosynthesis by miR444 Is Required for Ammonium-Triggered Inhibition of Root Growth
by
Yan, Jijun
, Liu, Yawen
, Chen, Xiaoying
, Yan, Yongsheng
, Chu, Jinfang
, Wang, Huacai
, Kong, Xiaoyu
, Fang, Rongxiang
, Jiao, Xiaoming
in
Ammonium Compounds - metabolism
/ Brassinosteroids - metabolism
/ Gene Expression Regulation, Plant
/ Oryza - metabolism
/ Plant Proteins - metabolism
/ Plant Roots - metabolism
/ SIGNALLING AND RESPONSE
2020
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Promotion of BR Biosynthesis by miR444 Is Required for Ammonium-Triggered Inhibition of Root Growth
by
Yan, Jijun
, Liu, Yawen
, Chen, Xiaoying
, Yan, Yongsheng
, Chu, Jinfang
, Wang, Huacai
, Kong, Xiaoyu
, Fang, Rongxiang
, Jiao, Xiaoming
in
Ammonium Compounds - metabolism
/ Brassinosteroids - metabolism
/ Gene Expression Regulation, Plant
/ Oryza - metabolism
/ Plant Proteins - metabolism
/ Plant Roots - metabolism
/ SIGNALLING AND RESPONSE
2020
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Do you wish to request the book?
Promotion of BR Biosynthesis by miR444 Is Required for Ammonium-Triggered Inhibition of Root Growth
by
Yan, Jijun
, Liu, Yawen
, Chen, Xiaoying
, Yan, Yongsheng
, Chu, Jinfang
, Wang, Huacai
, Kong, Xiaoyu
, Fang, Rongxiang
, Jiao, Xiaoming
in
Ammonium Compounds - metabolism
/ Brassinosteroids - metabolism
/ Gene Expression Regulation, Plant
/ Oryza - metabolism
/ Plant Proteins - metabolism
/ Plant Roots - metabolism
/ SIGNALLING AND RESPONSE
2020
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Promotion of BR Biosynthesis by miR444 Is Required for Ammonium-Triggered Inhibition of Root Growth
Journal Article
Promotion of BR Biosynthesis by miR444 Is Required for Ammonium-Triggered Inhibition of Root Growth
2020
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Overview
Rice (Oryza sativa), the staple food for almost half of the world's population, prefers ammonium (NH4
+) as the major nitrogen resource, and while NH4
+ has profound effects on rice growth and yields, the underlying regulatory mechanisms remain largely unknown. Brassinosteroids (BRs) are a class of steroidal hormones playing key roles in plant growth and development. In this study, we show that NH4
+ promotes BR biosynthesis through miR444 to regulate rice root growth. miR444 targeted five homologous MADS-box transcription repressors potentially forming homologous or heterogeneous complexes in rice. miR444 positively regulated BR biosynthesis through its MADS-box targets, which directly repress the transcription of BR-deficient dwarf 1 (OsBRD1), a key BR biosynthetic gene. NH4
+ induced the miR444-OsBRD1 signaling cascade in roots, thereby increasing the amount of BRs, whose biosynthesis and signaling were required for NH4
+-dependent root elongation inhibition. Consistently, miR444-overexpressing rice roots were hypersensitive to NH4
+ depending on BR biosynthesis, and overexpression of miR444's target, OsMADS57, resulted in rice hyposensitivity to NH4
+ in root elongation, which was associated with a reduction of BR content. In summary, our findings reveal a cross talk mechanism between NH4
+ and BR in which NH4
+ activates miR444-OsBRD1, an undescribed BR biosynthesis-promoting signaling cascade, to increase BR content, inhibiting root elongation in rice.
Publisher
American Society of Plant Biologists (ASPB),American Society of Plant Biologists
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