Rongrong Feng, Qi Chen, Yan Xu, Dehua Ji, Chaotian Xie, Wenlei Wang
{"title":"An animal-type Na<sup>+</sup>/K<sup>+</sup>-ATPase, <i>PhNKA2</i>, is involved in the salt tolerance of the intertidal macroalga <i>Pyropia haitanensis</i>.","authors":"Rongrong Feng, Qi Chen, Yan Xu, Dehua Ji, Chaotian Xie, Wenlei Wang","doi":"10.3389/fpls.2025.1571241","DOIUrl":null,"url":null,"abstract":"<p><p>Intertidal red algae, are more tolerant to salt stress than terrestrial plants, contain a Na<sup>+</sup> transporter (Na<sup>+</sup>/K<sup>+</sup>-ATPase) that is homologous to animal Na<sup>+</sup>/K<sup>+</sup>-ATPases. Although two Na<sup>+</sup>/K<sup>+</sup> pump genes from Pyropia/Porphyra were cloned and their differential expression patterns under salt stress were analyzed, the regulatory mechanism of Na<sup>+</sup>/K<sup>+</sup>-ATPase genes in Na<sup>+</sup> expulsion and K<sup>+</sup> retention process under salt stress remains largely unknown. In this study, we cloned and characterized the animal-type Na<sup>+</sup>/K<sup>+</sup>-ATPase gene <i>PhNKA2</i> in <i>Pyropia haitanensis</i>. The encoded protein was revealed to contain an N-terminal cation-transporting ATPase, E1/E2 ATPase, hydrolase, and a C-terminal cation-transporting ATPase. <i>PhNKA2</i> was highly conserved in <i>Porphyra</i>/<i>Pyropia</i>. The expression of <i>PhNKA2</i> in gametophytes was significantly induced by hypersalinity, while there was no obvious change in sporophytes. The heterologous expression of <i>PhNKA2</i> in <i>Chlamydomonas reinhardtii</i> clearly increased salt tolerance. Na<sup>+</sup> efflux and K<sup>+</sup> influx were significantly greater in the transgenic <i>C. reinhardtii</i> than in the wild-type control. Furthermore, yeast two-hybrid assays suggested that the interaction between the deubiquitinating enzyme USP5 and <i>PhNKA2</i> might be critical for the deubiquitination and stabilization of important proteins during the <i>P. haitanensis</i> response to salt stress. The interaction with MSRB2, DHPS, or GDCST may prevent the oxidation of <i>PhNKA2</i>, while actin depolymerization might stimulate Na<sup>+</sup>/K<sup>+</sup>-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.</p>","PeriodicalId":12632,"journal":{"name":"Frontiers in Plant Science","volume":"16 ","pages":"1571241"},"PeriodicalIF":4.1000,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12066774/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Plant Science","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3389/fpls.2025.1571241","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
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 PhNKA2 in Pyropia haitanensis. The encoded protein was revealed to contain an N-terminal cation-transporting ATPase, E1/E2 ATPase, hydrolase, and a C-terminal cation-transporting ATPase. PhNKA2 was highly conserved in Porphyra/Pyropia. The expression of PhNKA2 in gametophytes was significantly induced by hypersalinity, while there was no obvious change in sporophytes. The heterologous expression of PhNKA2 in Chlamydomonas reinhardtii clearly increased salt tolerance. Na+ efflux and K+ influx were significantly greater in the transgenic C. reinhardtii than in the wild-type control. Furthermore, yeast two-hybrid assays suggested that the interaction between the deubiquitinating enzyme USP5 and PhNKA2 might be critical for the deubiquitination and stabilization of important proteins during the P. haitanensis response to salt stress. The interaction with MSRB2, DHPS, or GDCST may prevent the oxidation of PhNKA2, 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.
期刊介绍:
In an ever changing world, plant science is of the utmost importance for securing the future well-being of humankind. Plants provide oxygen, food, feed, fibers, and building materials. In addition, they are a diverse source of industrial and pharmaceutical chemicals. Plants are centrally important to the health of ecosystems, and their understanding is critical for learning how to manage and maintain a sustainable biosphere. Plant science is extremely interdisciplinary, reaching from agricultural science to paleobotany, and molecular physiology to ecology. It uses the latest developments in computer science, optics, molecular biology and genomics to address challenges in model systems, agricultural crops, and ecosystems. Plant science research inquires into the form, function, development, diversity, reproduction, evolution and uses of both higher and lower plants and their interactions with other organisms throughout the biosphere. Frontiers in Plant Science welcomes outstanding contributions in any field of plant science from basic to applied research, from organismal to molecular studies, from single plant analysis to studies of populations and whole ecosystems, and from molecular to biophysical to computational approaches.
Frontiers in Plant Science publishes articles on the most outstanding discoveries across a wide research spectrum of Plant Science. The mission of Frontiers in Plant Science is to bring all relevant Plant Science areas together on a single platform.