{"title":"Isolation and Functional Determination of SKOR Potassium Channel in Purple Osier Willow, <i>Salix purpurea</i>.","authors":"Yahui Chen, Xuefeng Peng, Jijie Cui, Hongxia Zhang, Jiang Jiang, Zhizhong Song","doi":"10.1155/2021/6669509","DOIUrl":null,"url":null,"abstract":"<p><p>Potassium (K<sup>+</sup>) plays key roles in plant growth and development. However, molecular mechanism studies of K<sup>+</sup> nutrition in forest plants are largely rare. In plants, <i>SKOR</i> gene encodes for the outward rectifying Shaker-type K<sup>+</sup> channel that is responsible for the long-distance transportation of K<sup>+</sup> through xylem in roots. In this study, we determined a Shaker-type K<sup>+</sup> channel gene in purple osier (<i>Salix purpurea</i>), designated as <i>SpuSKOR</i>, and determined its function using a patch clamp electrophysiological system. SpuSKOR was closely clustered with poplar PtrSKOR in the phylogenetic tree. Quantitative real-time PCR (qRT-PCR) analyses demonstrated that <i>SpuSKOR</i> was predominantly expressed in roots, and expression decreased under K<sup>+</sup> depletion conditions. Patch clamp analysis via HEK293-T cells demonstrated that the activity of the SpuSKOR channel was activated when the cell membrane voltage reached at -10 mV, and the channel activity was enhanced along with the increase of membrane voltage. Outward currents were recorded and induced in response to the decrease of external K<sup>+</sup> concentration. Our results indicate that SpuSKOR is a typical voltage dependent outwardly rectifying K<sup>+</sup> channel in purple osier. This study provides theoretical basis for revealing the mechanism of K<sup>+</sup> transport and distribution in woody plants.</p>","PeriodicalId":13988,"journal":{"name":"International Journal of Genomics","volume":"2021 ","pages":"6669509"},"PeriodicalIF":2.6000,"publicationDate":"2021-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7932800/pdf/","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Genomics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1155/2021/6669509","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2021/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 4
Abstract
Potassium (K+) plays key roles in plant growth and development. However, molecular mechanism studies of K+ nutrition in forest plants are largely rare. In plants, SKOR gene encodes for the outward rectifying Shaker-type K+ channel that is responsible for the long-distance transportation of K+ through xylem in roots. In this study, we determined a Shaker-type K+ channel gene in purple osier (Salix purpurea), designated as SpuSKOR, and determined its function using a patch clamp electrophysiological system. SpuSKOR was closely clustered with poplar PtrSKOR in the phylogenetic tree. Quantitative real-time PCR (qRT-PCR) analyses demonstrated that SpuSKOR was predominantly expressed in roots, and expression decreased under K+ depletion conditions. Patch clamp analysis via HEK293-T cells demonstrated that the activity of the SpuSKOR channel was activated when the cell membrane voltage reached at -10 mV, and the channel activity was enhanced along with the increase of membrane voltage. Outward currents were recorded and induced in response to the decrease of external K+ concentration. Our results indicate that SpuSKOR is a typical voltage dependent outwardly rectifying K+ channel in purple osier. This study provides theoretical basis for revealing the mechanism of K+ transport and distribution in woody plants.
期刊介绍:
International Journal of Genomics is a peer-reviewed, Open Access journal that publishes research articles as well as review articles in all areas of genome-scale analysis. Topics covered by the journal include, but are not limited to: bioinformatics, clinical genomics, disease genomics, epigenomics, evolutionary genomics, functional genomics, genome engineering, and synthetic genomics.