LEAF TIP NECROSIS1 Plays a Pivotal Role in the Regulation of Multiple Phosphate Starvation Responses in Rice

被引:226
作者
Hu, Bin [1 ,2 ,3 ]
Zhu, Chenguang [1 ,2 ]
Li, Feng [1 ,2 ]
Tang, Jiuyou [1 ,2 ]
Wang, Yiqin [1 ,2 ]
Lin, Aihong [1 ,2 ,3 ]
Liu, Linchuan [1 ,2 ,3 ]
Che, Ronghui [1 ,2 ,3 ]
Chu, Chengcai [1 ,2 ]
机构
[1] Chinese Acad Sci, State Key Lab Plant Genom, Beijing 100101, Peoples R China
[2] Chinese Acad Sci, Natl Ctr Plant Gene Res Beijing, Inst Genet & Dev Biol, Beijing 100101, Peoples R China
[3] Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
VULGARIS L. ROOTS; ARABIDOPSIS-THALIANA; TRANSCRIPTION FACTOR; PHOSPHORUS DEFICIENCY; INCREASED EXPRESSION; MEDICAGO-TRUNCATULA; PLANTS; TRANSPORTER; ACID; HOMEOSTASIS;
D O I
10.1104/pp.110.170209
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Although phosphate (Pi) starvation signaling is well studied in Arabidopsis (Arabidopsis thaliana), it is still largely unknown in rice (Oryza sativa). In this work, a rice leaf tip necrosis1 (ltn1) mutant was identified and characterized. Map-based cloning identified LTN1 as LOC_Os05g48390, the putative ortholog of Arabidopsis PHO2, which plays important roles in Pi starvation signaling. Analysis of transgenic plants harboring a LTN1 promoter::beta-glucuronidase construct revealed that LTN1 was preferentially expressed in vascular tissues. The ltn1 mutant exhibited increased Pi uptake and translocation, which led to Pi overaccumulation in shoots. In association with enhanced Pi uptake and transport, some Pi transporters were up-regulated in the ltn1 mutant in the presence of sufficient Pi. Furthermore, the elongation of primary and adventitious roots was enhanced in the ltn1 mutant under Pi starvation, suggesting that LTN1 is involved in Pi-dependent root architecture alteration. Under Pi-sufficient conditions, typical Pi starvation responses such as stimulation of phosphatase and RNase activities, lipid composition alteration, nitrogen assimilation repression, and increased metal uptake were also activated in ltn1. Moreover, analysis of OsmiR399-overexpressing plants showed that LTN1 was down-regulated by OsmiR399. Our results strongly indicate that LTN1 is a crucial Pi starvation signaling component downstream of miR399 involved in the regulation of multiple Pi starvation responses in rice.
引用
收藏
页码:1101 / 1115
页数:15
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