State Key Laboratory of Crop Biology, National Research Center for Apple Engineering and Technology, College of Horticulture Science and Engineering, Shandong Agricultural University, Tai-An, Shandong 271018, China.
Qingdao Academy of Agricultural Science, Qing-Dao, Shandong 266100, China.
Plant Physiol. 2019 Jan;179(1):88-106. doi: 10.1104/pp.18.00289. Epub 2018 Oct 17.
SIZ1 (a SIZ/PIAS-type SUMO E3 ligase)-mediated small ubiquitin-like modifier (SUMO) modification of target proteins is important for various biological processes related to abiotic stress resistance in plants; however, little is known about its role in resistance toward iron (Fe) deficiency. Here, the SUMO E3 ligase MdSIZ1 was shown to be involved in the plasma membrane (PM) H-ATPase-mediated response to Fe deficiency. Subsequently, a basic helix-loop-helix transcription factor, MdbHLH104 (a homolog of Arabidopsis bHLH104 in apple), which acts as a key component in regulating PM H-ATPase-mediated rhizosphere acidification and Fe uptake in apples (), was identified as a direct target of MdSIZ1. MdSIZ1 directly sumoylated MdbHLH104 both in vitro and in vivo, especially under conditions of Fe deficiency, and this sumoylation was required for MdbHLH104 protein stability. Double substitution of K139R and K153R in MdbHLH104 blocked MdSIZ1-mediated sumoylation in vitro and in vivo, indicating that the K139 and K153 residues were the principal sites of SUMO conjugation. Moreover, the transcript level of the gene was substantially induced following Fe deficiency. overexpression exerted a positive influence on PM H-ATPase-mediated rhizosphere acidification and Fe uptake. Our findings reveal an important role for sumoylation in the regulation of PM H-ATPase-mediated rhizosphere acidification and Fe uptake during Fe deficiency in plants.
SIZ1(一种 SIZ/PIAS 型 SUMO E3 连接酶)介导的靶蛋白的小泛素样修饰物(SUMO)修饰对于与植物抗非生物胁迫相关的各种生物学过程很重要;然而,其在抵抗铁(Fe)缺乏方面的作用知之甚少。在这里,SUMO E3 连接酶 MdSIZ1 被证明参与质膜(PM)H-ATPase 介导的对 Fe 缺乏的反应。随后,碱性螺旋-环-螺旋转录因子 MdbHLH104(苹果中拟南芥 bHLH104 的同源物)被鉴定为 MdSIZ1 的直接靶标,该因子作为调节 PM H-ATPase 介导的根际酸化和苹果中 Fe 吸收的关键组成部分()。MdSIZ1 可在体外和体内直接对 MdbHLH104 进行 SUMO 化,尤其是在 Fe 缺乏的情况下,并且这种 SUMO 化对于 MdbHLH104 蛋白稳定性是必需的。MdbHLH104 中的 K139R 和 K153R 双取代在体外和体内均阻断了 MdSIZ1 介导的 SUMO 化,表明 K139 和 K153 残基是 SUMO 缀合的主要位点。此外,在 Fe 缺乏后,基因的转录水平显著升高。过表达对 PM H-ATPase 介导的根际酸化和 Fe 吸收具有积极影响。我们的发现揭示了 SUMO 化在植物 Fe 缺乏时调节 PM H-ATPase 介导的根际酸化和 Fe 吸收中的重要作用。