MicroRNA395 mediates regulation of sulfate accumulation and allocation in Arabidopsis thaliana

被引:242
|
作者
Liang, Gang [1 ,2 ]
Yang, Fengxi [1 ]
Yu, Diqiu [1 ]
机构
[1] Chinese Acad Sci, Key Lab Trop Forest Ecol, Xishuangbanna Trop Bot Garden, Kunming 650223, Yunnan, Peoples R China
[2] Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China
来源
PLANT JOURNAL | 2010年 / 62卷 / 06期
基金
国家高技术研究发展计划(863计划); 中国国家自然科学基金;
关键词
miR395; sulfate assimilation; sulfate transport; APS; SULTR2; 1; Arabidopsis thaliana; ATP SULFURYLASE; TRANSLATIONAL INHIBITION; PLANT; TRANSPORTERS; EXPRESSION; EVOLUTION; TARGETS; GENES; ROOT; TRANSLOCATION;
D O I
10.1111/j.1365-313X.2010.04216.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
P>Sulfur is a macronutrient that is necessary for plant growth and development. Sulfate, a major source of sulfur, is taken up by plant roots and transported into various tissues for assimilation. During sulfate limitation, expression of miR395 is significantly up-regulated. miR395 targets two families of genes, ATP sulfurylases (encoded by APS genes) and sulfate transporter 2;1 (SULTR2;1, also called AST68), both of which are involved in the sulfate metabolism pathway. Their transcripts are suppressed strongly in miR395-over-expressing transgenic Arabidopsis, which over-accumulates sulfate in the shoot but not in the root. APS1 knockdown mutants accumulate twice as much sulfate as the wild-type. By constructing APS4-RNAi transgenic plants, we found that silencing the APS4 gene also results in over-accumulation of sulfate. Even though miR395-over-expressing transgenic plants over-accumulate sulfate in the shoot, they display sulfur deficiency symptoms. Additionally, the distribution of sulfate from older to younger leaves is impaired in miR395-over-expressing plants, similar to a SULTR2;1 loss-of-function mutant. The aps1-1 sultr2;1 APS4-RNAi triply repressed mutants phenocopied miR395-over-expressing plants. Our research showed that miR395 is involved in the regulation of sulfate accumulation and allocation by targeting APS genes and SULTR2;1, respectively.
引用
收藏
页码:1046 / 1057
页数:12
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