期刊论文详细信息
Aquatic Biosystems
In silico analysis of high affinity potassium transporter (HKT) isoforms in different plants
Mahbobeh Zamani Babgohari2  Esmaeil Ebrahimie1  Ali Niazi2 
[1] School of Molecular & Biomedical Science, The University of Adelaide, Adelaide, Australia
[2] Biotechnology Institute, Shiraz University, Shiraz, Iran
关键词: Pathway discovery;    In silico synteny;    Regulatory elements;    Promoter;    Gene network;    HKT;   
Others  :  1089033
DOI  :  10.1186/2046-9063-10-9
 received in 2014-01-29, accepted in 2014-09-10,  发布年份 2014
PDF
【 摘 要 】

Background

High affinity potassium transporters (HKTs) are located in the plasma membrane of the vessels and have significant influence on salt tolerance in some plants. They exclude Na+ from the parenchyma cells to reduce Na+ concentration. Despite many studies, the underlying regulatory mechanisms and the exact functions of HKTs within different genomic backgrounds are relatively unknown. In this study, various bioinformatics techniques, including promoter analysis, identification of HKT-surrounding genes, and construction of gene networks, were applied to investigate the HKT regulatory mechanism.

Results

Promoter analysis showed that rice HKTs carry ABA response elements. Additionally, jasmonic acid response elements were detected on promoter region of TmHKT1;5. In silico synteny highlighted several unknown and new loci near rice, Arabidopsis thaliana and Physcomitrella patent HKTs, which may play a significant role in salt stress tolerance in concert with HKTs. Gene network prediction unravelled that crosstalk between jasmonate and ethylene reduces AtHKT1;1 expression. Furthermore, antiporter and transferase proteins were found in AtHKT1;1 gene network. Interestingly, regulatory elements on the promoter region of HKT in wild genotype (TmHKT1;5) were more frequent and variable than the ones in cultivated wheat (TaHKT1;5) which provides the possibility of rapid response and better understanding of environmental conditions for wild genotype.

Conclusion

Detecting ABA and jasmonic acid response elements on promoter regions of HKTs provide valuable clues on underlying regulatory mechanisms of HKTs. In silico synteny and pathway discovery indicated several candidates which act in concert with HKTs in stress condition. We highlighted different arrangement of regulatory elements on promoter region of wild wheat (TmHKT1;5) compared to bread wheat (TaHKT1;5) in this study.

【 授权许可】

   
2014 Zamani Babgohari et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20150124010139396.pdf 976KB PDF download
Figure 3. 107KB Image download
Figure 2. 97KB Image download
Figure 1. 49KB Image download
【 图 表 】

Figure 1.

Figure 2.

Figure 3.

【 参考文献 】
  • [1]Amtmann A, Sanders D: Mechanisms of Na+ uptake by plant cells. Adv Bot Res 1999, 29:75-112.
  • [2]James RA, Davenport RJ, Munns R: Physiological characterization of two genes for Na + exclusion in durum wheat, Nax1 and Nax2. Plant Physiol 2006, 142(4):1537-1547.
  • [3]Corratgé-Faillie C, Jabnoune M, Zimmermann S, Véry AA, Fizames C, Sentenac H: Potassium and sodium transport in non-animal cells: The Trk/Ktr/HKT transporter family. Cell. Mol. Life Sci 2010, 67:2511-2532.
  • [4]Durell SR, Guy HR: Structural models of the KtrB, TrkH, and Trk1,2 symporters based on the structure of the KcsA K + channel. Biophys 1999, 77:789-807.
  • [5]Marino-Ramirez L, Tharakaraman K, Bodenreider O, Spouge J, Landsman D: Identification of cis-regulatory elements in gene co-expression networks using A-GLAM. Methods Mol Biol 2009, 541:1-22.
  • [6]Mcclean PE, Mamidi S, McConnel M, Chikara S, Lee R: Synteny mapping between common bean and soybean reveals extensive blocks of shared loci. BMC Genomics 2010, 11(184):1474-2164.
  • [7]Alvo M, Liu Z, Williams A, Yauk C: Testing for mean and correlation changes in microarray experiments: an application for pathway analysis. BMC Bioinformatics 2010, 11:60. BioMed Central Full Text
  • [8]Hauser F, Horie T: A conserved primary salt tolerance mechanism mediated by HKT transporters: a mechanism for sodium exclusion and maintenance of high K(+)/Na(+) ratio in leaves during salinity stress. Plant Cell Environ 2010, 33(4):552-565.
  • [9]Byrt CS: Genes for sodium exclusion in wheat, PhD thesis. Australia: The University of Adelaide; 2008:1-155.
  • [10]Kotelnikova E, Ivanikova N, Kalinin A, Yuryev A, Daraselia N: Atlas of Signaling for Interpretation of Microarray Experiments. PLoS ONE 2010, 5(2):e9256. doi:10.1371/journal.pone.0009256
  • [11]Muffato M, Louis A, Poisnel CE, Crollius HR: A database and a browser to study gene synteny in modern and ancestral genomes. Genomicus 2012, 8:1119-1121.
  • [12]Obayashi T, Kinoshita K, Nakai K, Shibaoka M, Hayashi S, Saeki M, Shibata D, Saito K, Ohta H, ATTED-II: A database of co-expressed genes and cis elements for dentifying co-regulated gene groups in Arabidopsis. Nucleic Acids Res 2007, 35:D863-D869.
  • [13]Deihimi T, Niazi A, Ebrahimi M, Kajbaf K, Fanaee S, Bakhtiarizadeh MZ, Ebrahimie E: Finding the undiscovered roles of genes: an approach using mutual ranking of coexpressed genes and promoter architecture-case study: dual roles of thaumatin like proteins in biotic and abiotic stresses. Springer Plus 2012, 1:30. BioMed Central Full Text
  • [14]James RA, Blake C, Byrt CS, Munns R: Major genes for Na + exclusion, Nax1 and Nax2 (wheat HKT1;4 and HKT1;5), decrease Na + accumulation in bread wheat leaves under saline and waterlogged conditions. Exp Bot 2011, 62(8):2939-47.
  • [15]Zamani Babgohari M, Niazi A, Aboli-moghaddam AA, Deihimi D, Ebrahimie E: Genome-wide analysis of key salinity-tolerance transporter (HKT1;5) in wheat and wild wheat relatives (A and D genomes). In Vitro Cell Dev Biol-Plant 2012, 49:97-106.
  • [16]Molina C, Grotewold E: Genome wide analysis of Arabidopsis core promoters. BMC Genomics 2005, 6:25. BioMed Central Full Text
  • [17]Ashok Reddy D, Prasad BVLS, Mitra Chanchal K: Comparative analysis of core promoter region: Information content from mono and dinucleotide substitution matrices. Comput Biol Chem 2005, 30:58-62.
  • [18]Joshi CP: An inspection of the domain between putative TATA box and translation start site in 79 plant genes. Nucleic Acids Res 1987, 15:16.
  • [19]Grace ML, Chandrasekharan MB, Hall TC, Crow AJ: Sequence and Spacing of TATA Box Elements Are Critical for Accurate Initiation from the Phaseolin Promoter. Biol Chem 2004, 279(9):8102-8110.
  • [20]Butler JE, Kadonaga JT: The RNA polymerase II core promoter: a key component in the regulation of gene expression. Genes Dev 2002, 16:2583-2592.
  • [21]Sharma R, Katoch M, Govindappa N, Srivastava PS, Sastry K, Nabi Qazi G: Evaluation of the catalase promoter for expressing the alkaline xylanase gene (alx) in Aspergillus niger. FEMS Microbiol Lett 2011, 327:33-40.
  • [22]Byrt CS, Platten JD, Spielmeyer W, James RA, Lagudah ES, Dennis ES, Tester M, Munns R: HKT1;5-like cation transporters linked to Na + exclusion loci in wheat, Nax2 and Kna1. Plant Physiol 2007, 143(4):1918-28.
  • [23]Kusnetsov V, Landsberger M, Meurer J, Oelmüller R: The assembly of the CAAT-box binding complex at a photosynthesis gene promoter is regulated by light, cytokinin, and the stage of the Plastids. Biol Chem 1999, 274(50):36009-36014.
  • [24]Menke FLH, Champion AW, Kijne J, Memelink J: A novel jasmonate- and elicitor-responsive element in the periwinkle secondary metabolite biosynthetic gene Str interacts with a jasmonate- and elicitorinducible AP2-domain transcription factor ORCA2. EMBO 1999, 18(16):4455-4463.
  • [25]Lehmann J, Atzorn R, Brückner C, Reinbothe S, Leopold J, Wasternack C, Parthier B: Accumulation of jasmonate, abscisic acid, specific transcripts and proteins in osmotically stressed barley leaf segments. Planta 1995, 197:156-162.
  • [26]del Amor FM, Cuadra-Crespo P: Alleviation of salinity stress in broccoli using foliar urea or methyl-jasmonate: analysis of growth, gas exchange, and isotope composition. Plant Growth Regul 2010, 63:55-62.
  • [27]Platten JD, Cotsaftis O, Berthomieu P, Bohnert H, Davenport RJ, Fairbairn DJ, Horie T, Leigh RA, Lin HX, Luan S, Maser P, Pantoja O, Rodriguez-Navarro A, Schachtman DP, Schroeder JI, Sentenac H, Uozumi N, Very A, Zhu JK, Dennis ES, Tester M: Nomenclature for HKT transporters, key determinants of plant salinity tolerance. Trends Plant Sci 2006, 11(8):372-374.
  • [28]Mäser P, Gierth M, Schroeder JI: Molecular mechanisms of potassium and sodium uptake in plants. Plant Soil 2002, 247:43-54.
  • [29]Mundy J, Chua NH: Abscisic acid and water-stress induce the expression of a novel rice gene. EMBO 1988, 7(8):2279-86.
  • [30]Moghadam AA, Ebrahimie E, Taghavi SM, Niazi A, Zamani Babgohari M, Deihimi T, Djavaheri M, Ramezani A: How the nucleus and mitochondria communicate in energy production during stress: Nuclear MtATP6, an early-stress responsive gene, regulates the mitochondrial F1F0-ATP synthase complex. Mol Biotechnol 2013, 54:756-769.
  • [31]Plett D, Safwat G, Gilliham M, Moller IS, Roy S, Shirley N, Jacobs A, Johnson A, Tester M: Improved salinity tolerance of rice through cell type-specific expression of AtHKT1;1. PLoS One 2010, 5:e12571.
  • [32]Ren ZH, Gao JP, Li LG, Cai XL, Huang W, Chao DY, Zhu MZ, Wang ZY, Luan S, Lin HX: A rice quantitative trait locus for salt tolerance encodes a sodium transporter. Nat Genet 2005, 37:1141-1146.
  • [33]Kader MA, Seidel T, Golldack D, Lindberg S: Expressions of OsHKT1, OsHKT2, and OsVHA are differentially regulated under NaCl stress in salt-sensitive and salt-tolerant rice (Oryza sativa L.) cultivars. Exp Bot 2006, 57:4257-4268.
  • [34]Waters S, Gilliham M, Hrmova M: Plant high-affinity potassium (HKT) transporters involved in salinity tolerance: structural insights to probe differences in Ion Selectivity. Mol Sci 2013, 14:7660-7680.
  • [35]Meijer AH, Scarpella E, van Dijk EL, Qin L, Taal AJ, Rueb S, Harrington SE, McCouch SR, Schilperoort RA, Hoge JH: Transcriptional repression by Oshox1, a novel homeodomain leucine zipper protein from rice. Plant 1997, 11(2):263-76.
  • [36]G’omez-Cadenas A, TadeoFR TM, Primo-Millo E: Leaf abscission induced by ethylene in water-stressed intact seedlings of cleopatra mandarin requires previous abscisic acid accumulation in roots. Plant Physiol 1996, 112:401-408.
  • [37]Arbona V, Argamasilla R, G’omez-Cadenas A: Common and divergent physiological, hormonal and metabolic responses of Arabidopsis thaliana and Thellungiella halophila to water and salt stress. Plant Physiol 2010, 167:1342-1350.
  • [38]Lam E, Chua NH: Tetramer of a 21-base pair synthetic element confers seed expression and transcriptional enhancement in response to water stress and abscisic acid. Biol Chem 1991, 266(26):17131-5.
  • [39]Mundy J, Yamaguchi-Shinozaki K, Chua NH: Nuclear proteins bind conserved elements in the abscisic acid-responsive promoter of a rice rab gene. Proc Natl Acad Sci 1990, 87(4):1406-10.
  • [40]Zhu JK: Regulation of ion homeostasis under salt stress. Curr Opin Plant Biol 2003, 6(5):441-5.
  • [41]Almeida P, Katschnig DH, de Boer D: HKT Transporters—State of the Art. Mol Sci 2013, 14:20359-20385.
  • [42]Ramezani A, Niazi A, Abolimoghadam AA, Zamani Babgohari M, Deihimi T, Ebrahimi M, Akhtardanesh H, Ebrahimie E: Quantitative expression analysis of TaSOS1 and TaSOS4 genes in cultivated and wild wheat plants under salt stress. Mol Biotechnol 2012, 53:189-197.
  • [43]Moon A, Prinsen E, Bauw G, Van Montagu M: Antagonistic effects of abscisic acid and jasmonates on salt stress-lnducible transcripts in rice roots. Plant Cell 1997, 9:2243-2259.
  • [44]Ebrahimie M, Esmaeili F, Cheraghi S, Houshmand F, Shabani L, Ebrahimie E: Efficient and Simple Production of Insulin-Producing Cells from Embryonal Carcinoma Stem Cells Using Mouse Neonate Pancreas Extract, As a Natural Inducer. PLoS ONE 2014, 9:e90885.
  • [45]Obayashi T, Kinoshita K: Rank of correlation coefficient as a comparable measure for biological significance of gene coexpression. DNA Res 2009, 16:249-60.
  • [46]Hosseinpour B, Bakhtiarizadeh MR, Khosravi P, Ebrahimie E: Predicting distinct organization of transcription factor binding sites on the promoter regions: a new genome-based approach to expand human embryonic stem cell regulatory network. Gene 2013, 531:212-219.
  文献评价指标  
  下载次数:34次 浏览次数:27次