Trifurcate Feed-Forward Regulation of Age-Dependent Cell Death Involving miR164 in Arabidopsis

被引:583
作者
Kim, Jin Hee [1 ]
Woo, Hye Ryun [1 ]
Kim, Jeongsik [1 ]
Lim, Pyung Ok [2 ]
Lee, In Chul [1 ]
Choi, Seung Hee [1 ]
Hwang, Daehee [3 ,4 ]
Nam, Hong Gil [1 ,4 ]
机构
[1] Pohang Univ Sci & Technol, Div Mol Life Sci, Pohang 790784, South Korea
[2] Cheju Natl Univ, Dept Sci Educ, Cheju, South Korea
[3] Pohang Univ Sci & Technol, Dept Chem Engn, Pohang 790784, South Korea
[4] Pohang Univ Sci & Technol, Sch Interdisciplinary Biosci & Bioengn, Pohang 790784, South Korea
关键词
LATERAL ROOT DEVELOPMENT; LEAF SENESCENCE; SIGNALING PATHWAYS; STRESS RESPONSES; THALIANA; MICRORNA; ETHYLENE; TRANSCRIPTOME; TARGETS;
D O I
10.1126/science.1166386
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Aging induces gradual yet massive cell death in higher organisms, including annual plants. Even so, the underlying regulatory mechanisms are barely known, despite the long- standing interest in this topic. Here, we demonstrate that ORE1, which is a NAC ( NAM, ATAF, and CUC) transcription factor, positively regulates aging- induced cell death in Arabidopsis leaves. ORE1 expression is up- regulated concurrently with leaf aging by EIN2 but is negatively regulated by miR164. miR164 expression gradually decreases with aging through negative regulation by EIN2, which leads to the elaborate up- regulation of ORE1 expression. However, EIN2 still contributes to aging- induced cell death in the absence of ORE1. The trifurcate feed- forward pathway involving ORE1, miR164, and EIN2 provides a highly robust regulation to ensure that aging induces cell death in Arabidopsis leaves.
引用
收藏
页码:1053 / 1057
页数:5
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