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拟南芥 BRUTUS-LIKE E3 连接酶通过靶向转录因子 FIT 进行循环来负调控铁的摄取。

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

机构信息

Department of Biological Chemistry, John Innes Centre, Norwich NR4 7UH, United Kingdom.

School of Biological Sciences, University of East Anglia, Norwich NR4 7TJ, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 2019 Aug 27;116(35):17584-17591. doi: 10.1073/pnas.1907971116. Epub 2019 Aug 14.

DOI:10.1073/pnas.1907971116
PMID:31413196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6717287/
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 and provide evidence that they target the transcription factor FIT, a key regulator of Fe uptake, for degradation. The 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.

摘要

生物体需要平衡铁(Fe)的充足摄取和可能的毒性。在植物根中,一组摄取基因在缺铁时被转录激活,但当 Fe 变得可用时,这种反应是如何失活的尚不清楚。在这里,我们描述了 2 个部分冗余的 E3 泛素连接酶 BRUTUS-LIKE1(BTSL1)和 BTSL2 在中的功能,并提供证据表明它们将 FIT 的转录因子作为降解的靶标,FIT 是 Fe 摄取的关键调节剂。双突变体未能有效地下调 FIT 控制的基因的转录,并且在根和叶中积累了有毒水平的 Fe。BTSL1 和 BTSL2 的 C 端结构域表现出 E3 连接酶活性,并与 FIT 相互作用,但不与其二聚体伙伴 bHLH39 相互作用。BTSL 蛋白能够在体外多泛素化 FIT 并促进体内 FIT 降解。因此,FIT 的翻译后控制对于防止过量的 Fe 摄取至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5e8/6717287/afc49ca48a3a/pnas.1907971116fig07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5e8/6717287/f54a0e0fdb73/pnas.1907971116fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5e8/6717287/b1ed51d2ab07/pnas.1907971116fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5e8/6717287/049b3bc80191/pnas.1907971116fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5e8/6717287/ed8f4dae804a/pnas.1907971116fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5e8/6717287/ecca099e91d3/pnas.1907971116fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5e8/6717287/1b682d285d21/pnas.1907971116fig06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5e8/6717287/afc49ca48a3a/pnas.1907971116fig07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5e8/6717287/f54a0e0fdb73/pnas.1907971116fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5e8/6717287/b1ed51d2ab07/pnas.1907971116fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5e8/6717287/049b3bc80191/pnas.1907971116fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5e8/6717287/ed8f4dae804a/pnas.1907971116fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5e8/6717287/ecca099e91d3/pnas.1907971116fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5e8/6717287/1b682d285d21/pnas.1907971116fig06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5e8/6717287/afc49ca48a3a/pnas.1907971116fig07.jpg

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