Tomoyuki Okada, Sousuke Yamane, M. Yamaguchi, K. Kato, A. Shinmyō, Yuta Tsunemitsu, K. Iwasaki, D. Ueno, T. Demura
{"title":"Characterization of rice KT/HAK/KUP potassium transporters and K+ uptake by HAK1 from Oryza sativa.","authors":"Tomoyuki Okada, Sousuke Yamane, M. Yamaguchi, K. Kato, A. Shinmyō, Yuta Tsunemitsu, K. Iwasaki, D. Ueno, T. Demura","doi":"10.5511/PLANTBIOTECHNOLOGY.18.0308A","DOIUrl":null,"url":null,"abstract":"Plant high-affinity K+ (HAK) transporters are divided into four major clusters. Cluster I transporters, in particular, are thought to have high-affinity for K+. Of the 27 HAK genes in rice, eight HAK transporters belong to cluster I. In this study, we investigated the temporal expression patterns during K+ deficiency and K+ transport activity of these eight HAK transporters. The expression of seven HAK genes except OsHAK20 was detected. Expression of OsHAK1, OsHAK5 and OsHAK21 was induced in response to K+ deficiency; however, that of other genes was not. Six of the eight HAK transporters-OsHAK1, OsHAK5, OsHAK19, OsHAK20, OsHAK21, and OsHAK27-complemented the K+-transporter-deficient yeast or bacterial strain. Further, the yeast cells expressing OsHAK1 were more sensitive to Na+ than those expressing OsHAK5. Mutant analysis showed that the high-affinity K+ uptake activity was almost undetectable in oshak1 mutants in a low-K+ medium (0.02 mM). In addition, the high-affinity K+ uptake activity of wild-type plants was inhibited by mild salt stress (20 mM NaCl); however, Na+ permeability of OsHAK1 was not detected in Escherichia coli cells. The high-affinity K+ uptake activity by leaf blades was detected in wild-type plants, while it was not detected in oshak1 mutants. Our results suggest that OsHAK1 and OsHAK5 are the two important components of cluster I corresponding to low-K+ conditions, and that the transport activity of OsHAK1, unlike that of OsHAK5, is sensitive to Na+. Further, OsHAK1 is suggested to involve in foliar K+ uptake.","PeriodicalId":20411,"journal":{"name":"Plant Biotechnology","volume":"35 2 1","pages":"101-111"},"PeriodicalIF":1.4000,"publicationDate":"2018-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.5511/PLANTBIOTECHNOLOGY.18.0308A","citationCount":"20","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Biotechnology","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.5511/PLANTBIOTECHNOLOGY.18.0308A","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 20
Abstract
Plant high-affinity K+ (HAK) transporters are divided into four major clusters. Cluster I transporters, in particular, are thought to have high-affinity for K+. Of the 27 HAK genes in rice, eight HAK transporters belong to cluster I. In this study, we investigated the temporal expression patterns during K+ deficiency and K+ transport activity of these eight HAK transporters. The expression of seven HAK genes except OsHAK20 was detected. Expression of OsHAK1, OsHAK5 and OsHAK21 was induced in response to K+ deficiency; however, that of other genes was not. Six of the eight HAK transporters-OsHAK1, OsHAK5, OsHAK19, OsHAK20, OsHAK21, and OsHAK27-complemented the K+-transporter-deficient yeast or bacterial strain. Further, the yeast cells expressing OsHAK1 were more sensitive to Na+ than those expressing OsHAK5. Mutant analysis showed that the high-affinity K+ uptake activity was almost undetectable in oshak1 mutants in a low-K+ medium (0.02 mM). In addition, the high-affinity K+ uptake activity of wild-type plants was inhibited by mild salt stress (20 mM NaCl); however, Na+ permeability of OsHAK1 was not detected in Escherichia coli cells. The high-affinity K+ uptake activity by leaf blades was detected in wild-type plants, while it was not detected in oshak1 mutants. Our results suggest that OsHAK1 and OsHAK5 are the two important components of cluster I corresponding to low-K+ conditions, and that the transport activity of OsHAK1, unlike that of OsHAK5, is sensitive to Na+. Further, OsHAK1 is suggested to involve in foliar K+ uptake.
植物高亲和力K+转运蛋白可分为四大类。特别是簇I转运蛋白被认为对K+具有高亲和力。在水稻的27个HAK基因中,有8个HAK转运蛋白属于I簇。在本研究中,我们研究了K+缺乏期间的时间表达模式和这8个HAK转运蛋白的K+转运活性。检测到除OsHAK20外的7个HAK基因的表达。OsHAK1、OsHAK5和OsHAK21的表达是响应K+缺乏而诱导的;然而,其他基因则不然。八种HAK转运蛋白OsHAK1、OsHAK5、OsHAK19、OsHAK20、OsHAK21和OsHAK27中的六种补充了缺乏K+转运蛋白的酵母或细菌菌株。此外,表达OsHAK1的酵母细胞比表达OsHAK5的酵母细胞对Na+更敏感。突变体分析表明,在低K+培养基(0.02 mM)。此外,野生型植物的高亲和力K+吸收活性受到轻度盐胁迫的抑制(20 mM NaCl);但是在大肠杆菌细胞中未检测到OsHAK1的Na+渗透性。叶片对K+的高亲和力吸收活性在野生型植物中检测到,而在oshak1突变体中没有检测到。我们的结果表明,OsHAK1和OsHAK5是簇I的两个重要组成部分,对应于低K+条件,并且OsHAK1的转运活性不同于OsHAK5,对Na+敏感。此外,OsHAK1被认为参与了叶片K+的吸收。
期刊介绍:
Plant Biotechnology is an international, open-access, and online journal, published every three months by the Japanese Society for Plant Biotechnology. The journal, first published in 1984 as the predecessor journal, “Plant Tissue Culture Letters” and became its present form in 1997 when the society name was renamed to Japanese Society for Plant Cell and Molecular Biology, publishes findings in the areas from basic- to application research of plant biotechnology. The aim of Plant Biotechnology is to publish original and high-impact papers, in the most rapid turnaround time for reviewing, on the plant biotechnology including tissue culture, production of specialized metabolites, transgenic technology, and genome editing technology, and also on the related research fields including molecular biology, cell biology, genetics, plant breeding, plant physiology and biochemistry, metabolic engineering, synthetic biology, and bioinformatics.