共 41 条
Arabidopsis BRUTUS-LIKE E3 ligases negatively regulate iron uptake by targeting transcription factor FIT for recycling
被引:104
作者:
Rodriguez-Celma, Jorge
[1
,2
]
Connorton, James M.
[1
,2
]
Kruse, Inga
[1
,5
]
Green, Robert T.
[1
]
Franceschetti, Marina
[1
]
Chen, Yi-Tze
[3
]
Cui, Yan
[4
]
Ling, Hong-Qing
[4
]
Yeh, Kuo-Chen
[3
]
Balk, Janneke
[1
,2
]
机构:
[1] John Innes Ctr, Dept Biol Chem, Norwich NR4 7UH, Norfolk, England
[2] Univ East Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England
[3] Acad Sinica, Agr Biotechnol Res Ctr, Taipei 11529, Taiwan
[4] Chinese Acad Sci, Inst Genet & Dev Biol, Beijing 100101, Peoples R China
[5] Univ Strathclyde, Strathclyde Inst Pharm & Biomed Sci, Glasgow G1 1XQ, Lanark, Scotland
来源:
基金:
英国生物技术与生命科学研究理事会;
欧盟地平线“2020”;
关键词:
iron;
ubiquitin;
bHLH transcription factor;
dicotyledon;
micronutrient;
UPTAKE SYSTEM;
DEFICIENCY;
HOMEOSTASIS;
MOBILIZATION;
DEGRADATION;
INTERACTS;
RESPONSES;
PLANTS;
ROOTS;
D O I:
10.1073/pnas.1907971116
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:
Organisms need to balance sufficient uptake of iron (Fe) with possible toxicity. In plant roots, a regulon of uptake genes is transcriptionally activated under Fe deficiency, but it is unknown how this response is inactivated when Fe becomes available. Here we describe the function of 2 partially redundant E3 ubiquitin ligases, BRUTUS-LIKE1 (BTSL1) and BTSL2, in Arabidopsis thaliana and provide evidence that they target the transcription factor FIT, a key regulator of Fe uptake, for degradation. The btsl double mutant failed to effectively down-regulate the transcription of genes controlled by FIT, and accumulated toxic levels of Fe in roots and leaves. The C-terminal domains of BTSL1 and BTSL2 exhibited E3 ligase activity, and interacted with FIT but not its dimeric partner bHLH39. The BTSL proteins were able to poly-ubiquitinate FIT in vitro and promote FIT degradation in vivo. Thus, posttranslational control of FIT is critical to prevent excess Fe uptake.
引用
收藏
页码:17584 / 17591
页数:8
相关论文