N6-Methyladenosine RNA Modification Regulates Shoot Stem Cell Fate in Arabidopsis

被引:359
作者
Shen, Lisha [1 ,2 ]
Liang, Zhe [1 ,2 ]
Gu, Xiaofeng [3 ]
Chen, Ying [1 ,2 ]
Teo, Zhi Wei Norman [1 ,2 ]
Hou, Xingliang [4 ]
Cai, Weiling Maggie [5 ]
Dedon, Peter C. [5 ]
Liu, Lu [1 ,2 ]
Yu, Hao [1 ,2 ]
机构
[1] Natl Univ Singapore, Temasek Life Sci Lab, 10 Sci Dr 4, Singapore 117543, Singapore
[2] Natl Univ Singapore, Dept Biol Sci, 10 Sci Dr 4, Singapore 117543, Singapore
[3] Chinese Acad Agr Sci, Biotechnol Res Inst, Beijing 100081, Peoples R China
[4] Chinese Acad Sci, South China Bot Garden, Guangzhou 510650, Guangdong, Peoples R China
[5] Singapore MIT Alliance Res & Technol, CREATE, Singapore 138602, Singapore
基金
新加坡国家研究基金会;
关键词
MESSENGER-RNA; M(6)A RNA; NUCLEAR-RNA; ADENOSINE METHYLATION; GENE; MERISTEM; WUSCHEL; BINDING; N6-METHYLADENOSINE; REPRESSION;
D O I
10.1016/j.devcel.2016.06.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
N-6-Methyladenosine (m(6)A) represents the most prevalent internal modification on mRNA and requires a multicomponent m(6)A methyltransferase complex in mammals. How their plant counterparts determine the global m(6)A modification landscape and its molecular link to plant development remain unknown. Here we show that FKBP12 INTERACTING PROTEIN 37 KD (FIP37) is a core component of the m(6)A methyltransferase complex, which underlies control of shoot stem cell fate in Arabidopsis. The mutants lacking FIP37 exhibit massive overproliferation of shoot meristems and a transcriptome-wide loss of m(6)A RNA modifications. We further demonstrate that FIP37 mediates m(6)A RNA modification on key shoot meristem genes inversely correlated with their mRNA stability, thus confining their transcript levels to prevent shoot meristem overproliferation. Our results suggest an indispensable role of FIP37 in mediating m(6)A mRNA modification, which is required for maintaining the shoot meristem as a renewable source for continuously producing all aerial organs in plants.
引用
收藏
页码:186 / 200
页数:15
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