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Arabidopsis BRUTUS-LIKE E3 ligases negatively regulate iron uptake by targeting transcription factor FIT for recycling.


ABSTRACT: 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.

SUBMITTER: Rodriguez-Celma J 

PROVIDER: S-EPMC6717287 | biostudies-literature | 2019 Aug

REPOSITORIES: biostudies-literature

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Arabidopsis BRUTUS-LIKE E3 ligases negatively regulate iron uptake by targeting transcription factor FIT for recycling.

Rodríguez-Celma Jorge J   Connorton James M JM   Kruse Inga I   Green Robert T RT   Franceschetti Marina M   Chen Yi-Tze YT   Cui Yan Y   Ling Hong-Qing HQ   Yeh Kuo-Chen KC   Balk Janneke J  

Proceedings of the National Academy of Sciences of the United States of America 20190814 35


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 <i>Arabidopsis thaliana</i> and provide evidence that they target the transcription factor FIT, a key regulator of Fe uptake, for degra  ...[more]

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