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拟南芥IRT1铁转运蛋白的诞生、生命历程与死亡:亲密伙伴与对手的作用

Birth, life and death of the Arabidopsis IRT1 iron transporter: the role of close friends and foes.

作者信息

Abuzeineh Anas, Vert Grégory, Zelazny Enric

机构信息

Institute for Plant Sciences of Montpellier (IPSiM), CNRS, University of Montpellier, INRAE, Montpellier SupAgro, 34060, Montpellier, France.

Plant Science Research Laboratory (LRSV), UMR5546, CNRS/Toulouse, INP/University of Toulouse 3, 31320, Auzeville Tolosane, France.

出版信息

Planta. 2022 Nov 11;256(6):112. doi: 10.1007/s00425-022-04018-7.

Abstract

IRT1 intracellular dynamics and function are finely controlled through protein-protein interactions. In plants, iron uptake from the soil is tightly regulated to allow optimal growth and development. Iron acquisition in Arabidopsis root epidermal cells requires the IRT1 transporter, which also mediates the entry of non-iron metals. In this mini-review, we describe how protein-protein interactions regulate IRT1 intracellular dynamics and IRT1-mediated metal uptake to maintain iron homeostasis. Recent interactomic data provided interesting clues on IRT1 secretion and the putative involvement of COPI- and COPII-mediated pathways. Once delivered to the plasma membrane, IRT1 can interact with other components of the iron uptake machinery to form an iron acquisition complex that likely optimizes iron entrance in root epidermal cells. Then, IRT1 may be internalized from the plasma membrane. In the past decade, IRT1 endocytosis emerged as an essential mechanism to control IRT1 subcellular localization and thus to tune iron uptake. Interestingly, IRT1 endocytosis and degradation are regulated by its non-iron metal substrates in an ubiquitin-dependent manner, which requires a set of interacting-proteins including kinases, E3 ubiquitin ligases and ESCRT complex subunits. This mechanism is essential to avoid non-iron metal overload in Arabidopsis when the iron is scarce.

摘要

IRT1的细胞内动态和功能通过蛋白质-蛋白质相互作用得到精细调控。在植物中,从土壤中吸收铁受到严格调控,以实现最佳生长和发育。拟南芥根表皮细胞中的铁获取需要IRT1转运蛋白,它也介导非铁金属的进入。在这篇小型综述中,我们描述了蛋白质-蛋白质相互作用如何调节IRT1的细胞内动态以及IRT1介导的金属吸收,以维持铁稳态。最近的相互作用组学数据为IRT1的分泌以及COP I和COP II介导途径的可能参与提供了有趣的线索。一旦IRT1被转运到质膜,它可以与铁吸收机制的其他成分相互作用,形成一个铁获取复合物,该复合物可能优化根表皮细胞中铁的进入。然后,IRT1可能从质膜内化。在过去十年中,IRT1的内吞作用成为控制IRT1亚细胞定位从而调节铁吸收的一种重要机制。有趣的是,IRT1的内吞作用和降解由其非铁金属底物以泛素依赖的方式调控,这需要一组相互作用的蛋白质,包括激酶、E3泛素连接酶和ESCRT复合物亚基。当铁缺乏时,这种机制对于避免拟南芥中非铁金属过载至关重要。

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