Feng Rongrong, Chen Qi, Xu Yan, Ji Dehua, Xie Chaotian, Wang Wenlei
Fisheries College, Jimei University, Xiamen, China.
State Key Laboratory of Mariculture Breeding (Jimei University), Ningde, China.
Front Plant Sci. 2025 Apr 28;16:1571241. doi: 10.3389/fpls.2025.1571241. eCollection 2025.
Intertidal red algae, are more tolerant to salt stress than terrestrial plants, contain a Na transporter (Na/K-ATPase) that is homologous to animal Na/K-ATPases. Although two Na/K pump genes from Pyropia/Porphyra were cloned and their differential expression patterns under salt stress were analyzed, the regulatory mechanism of Na/K-ATPase genes in Na expulsion and K retention process under salt stress remains largely unknown. In this study, we cloned and characterized the animal-type Na/K-ATPase gene in . The encoded protein was revealed to contain an N-terminal cation-transporting ATPase, E1/E2 ATPase, hydrolase, and a C-terminal cation-transporting ATPase. was highly conserved in /. The expression of in gametophytes was significantly induced by hypersalinity, while there was no obvious change in sporophytes. The heterologous expression of in clearly increased salt tolerance. Na efflux and K influx were significantly greater in the transgenic than in the wild-type control. Furthermore, yeast two-hybrid assays suggested that the interaction between the deubiquitinating enzyme USP5 and might be critical for the deubiquitination and stabilization of important proteins during the response to salt stress. The interaction with MSRB2, DHPS, or GDCST may prevent the oxidation of , while actin depolymerization might stimulate Na/K-ATPase-dependent membrane trafficking. The results of this study provide new insights into the salt tolerance of intertidal seaweed as well as the underlying molecular basis.
潮间带红藻比陆生植物更耐盐胁迫,含有一种与动物钠钾ATP酶同源的钠转运蛋白(钠钾ATP酶)。尽管克隆了来自紫菜属的两个钠钾泵基因,并分析了它们在盐胁迫下的差异表达模式,但盐胁迫下钠钾ATP酶基因在排钠和保钾过程中的调控机制仍基本未知。在本研究中,我们克隆并鉴定了[具体物种]中的动物型钠钾ATP酶基因。所编码的蛋白质显示含有一个N端阳离子转运ATP酶、E1/E2 ATP酶、水解酶和一个C端阳离子转运ATP酶。[具体基因]在[具体物种]中高度保守。在配子体中,[具体基因]的表达受到高盐度的显著诱导,而在孢子体中没有明显变化。[具体基因]在[具体物种]中的异源表达明显提高了耐盐性。转基因[具体物种]中的钠外流和钾内流明显大于野生型对照。此外,酵母双杂交试验表明,去泛素化酶USP5与[具体基因]之间的相互作用可能在[具体物种]对盐胁迫的反应中对重要蛋白质的去泛素化和稳定至关重要。与MSRB2、DHPS或GDCST的相互作用可能防止[具体基因]的氧化,而肌动蛋白解聚可能刺激钠钾ATP酶依赖性膜运输。本研究结果为潮间带海藻的耐盐性及其潜在分子基础提供了新的见解。