A remorin gene SiREM6, the target gene of SiARDP, from foxtail millet (Setaria italica) promotes high salt tolerance in transgenic Arabidopsis

PLoS ONE

Volumn 9, Issue 6, 2014, Pages

  Yue, Jing ^a   Li, Cong ^a   Liu, Yuwei ^a   Yu, Jingjuan ^a  

^a CHINA AGRICULTURAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ABRE BINDING TRANSCRIPTION FACTOR AREB1; ABSCISIC ACID; ELECTROLYTE; PROLINE; REMORIN PROTEIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR ADRP; UNCLASSIFIED DRUG; VEGETABLE PROTEIN; CARRIER PROTEIN; PHOSPHOPROTEIN; REMORIN;

ABIOTIC STRESS; ABSCISIC ACID RESPONSIVE ELEMENT; AMINO TERMINAL SEQUENCE; ARABIDOPSIS; ARDP GENE; AREB1 GENE; ARTICLE; CONTROLLED STUDY; DEHYDRATION RESPONSIVE ELEMENT; DNA RESPONSIVE ELEMENT; DROUGHT STRESS; ELECTRIC CONDUCTIVITY; ELECTROLYTE LEAKAGE; ELECTRON MICROSCOPY; FOXTAIL MILLET; GENE FUNCTION; GENE IDENTIFICATION; GENE OVEREXPRESSION; GENE SEQUENCE; GENE TARGETING; GENETIC ANALYSIS; GENETIC TRANSCRIPTION; GERMINATION; HOMOZYGOSITY; IN VITRO STUDY; LOW TEMPERATURE; MOLECULAR CLONING; NONHUMAN; OLIGOMERIZATION; PHENOTYPE; PHYLOGENY; PLANT GENE; PROMOTER REGION; PROTEIN CONTENT; PROTEIN DNA BINDING; PROTEIN PHOSPHORYLATION; REM6 GENE; REMORIN GENE; SALT STRESS; SALT TOLERANCE; SIGNAL TRANSDUCTION; SURVIVAL RATE; TRANSGENIC PLANT; TRANSGENICS; CHEMISTRY; DRUG EFFECTS; GENETICS; GROWTH, DEVELOPMENT AND AGING; METABOLISM; PHYSIOLOGICAL STRESS; PHYSIOLOGY; PROTEIN MULTIMERIZATION; PROTEIN QUATERNARY STRUCTURE; SEEDLING; SETARIA (PLANT);

ABSCISIC ACID; ARABIDOPSIS; CARRIER PROTEINS; GERMINATION; PHOSPHOPROTEINS; PLANT PROTEINS; PLANTS, GENETICALLY MODIFIED; PROMOTER REGIONS, GENETIC; PROTEIN MULTIMERIZATION; PROTEIN STRUCTURE, QUATERNARY; SALT-TOLERANCE; SEEDLING; SETARIA PLANT; STRESS, PHYSIOLOGICAL; TRANSCRIPTION FACTORS;

EID: 84903542212     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0100772     Document Type: Article

References (46)

1. Tuteja N (2007) Mechanisms of high salinity tolerance in plants. Methods Enzymol 428: 419-438.
2. Yeo AR, Flowers TJ (1984) Nonosmotic effects of polyethylene glycols upon sodium transport and sodium-potassium selectivity by rice roots. Plant Physiol 75: 298-303.
3. Waditee R, Bhuiyan MN, Rai V, Aoki K, Tanaka Y, et al. (2005) Genes for direct methylation of glycine provide high levels of glycinebetaine and abiotic-stress tolerance in Synechococcus and Arabidopsis. Proc Natl Acad Sci USA 102: 1318-1323. (Pubitemid 40209168)
4. Xiong L, Schumaker KS, Zhu JK (2002) Cell signaling during cold, drought and salt stress. Plant Cell 14: S165-S183. (Pubitemid 34609237)
5. Checker VG, Khurana P (2013) Molecular and functional characterization of mulberry EST encoding remorin (MiREM) involved in abiotic stress. Plant Cell Rep 32: 1729-1741.
6. Farmer EE, Pearce G, Ryan CA (1989) In vitro phosphorylation of plant plasma membrane proteins in response to the proteinase inhibitor inducing factor. Proc Natl Acad Sci USA 86: 1539-1542.
7. Jacinto T, Farmer EE, Ryan CA (1993) Purification of potato leaf plasma membrane protein pp34, a protein phosphorylated in response to oligogalacturonide signals for defense and development. Plant Physiol 103: 1393-1397. (Pubitemid 2027588)
8. Raffaele S, Mongrand S, Gamas P, Niebel A, Ott T (2007) Genome-wide annotation of remorins, a plant-specific protein family: evolutionary and functional perspectives. Plant Physiol 145: 593-600. (Pubitemid 350127592)
9. Fedorova M, van de Mortel J, Matsumoto PA, Cho J, Town CD, et al. (2002) Genome-wide identification of nodule-specific transcripts in the model legume Medicago truncatula. Plant Physiol 130: 519-537. (Pubitemid 35224763)
10. Coaker GL, Willard B, Kinter M, Stockinger EJ, Francis DM (2004) Proteomic analysis of resistance mediated by Rcm 2.0 and Rcm 5.1, two loci controlling resistance to bacterial canker of tomato. Mol Plant Microbe Interact 17: 1019-1028. (Pubitemid 39098890)
11. Sánchez-Morán E, Mercier R, Higgins JD, Armstrong SJ, Jones GH, et al. (2005) A strategy to investigate the plant meiotic proteome. Cytogenet Genome Res 109: 181-189. (Pubitemid 40470321)
12. Kistner C, Winzer T, Pitzschke A, Mulder L, Sato S, et al. (2005) Seven Lotus japonicus genes required for transcriptional reprogramming of the root during fungal and bacterial symbiosis. Plant Cell 17: 2217-2229. (Pubitemid 41672942)
13. Ofosu-Anim J, Offei SK, Yamaki S (2006) Pistil receptivity, pollen tube growth and gene expression during early fruit development in sweet pepper (Capsicum annum). Int J Agric Biol 8: 576-579.
14. Marin M, Ott T (2012) Phosphorylation of intrinsically disordered regions in remorin proteins. Front Plant Sci 3: 86.
15. Bariola P, Retelska D, Stasiak A, Kammerer R, Fleming A, et al. (2004) Remorins fom a novel family of coiled coil-foming oligomeric and filamentous proteins associated with apical, vascular and embryonic tissues in plants. Plant Mol Biol 55: 579-594. (Pubitemid 40653986)
16. Wienkoop S, Saalbach G (2003) Proteome analysis. Novel proteins identified at the peribacteroid membrane from Lotus japonicus root nodules. Plant Physiol 131: 1080-1090. (Pubitemid 36400345)
17. El Yahyaoui F, Kuster H, Ben Amor B, Hohnjec N, Puhler A, et al. (2004) Expression profiling in Medicago truncatula identifies more than 750 genes differentially expressed during nodulation, including many potential regulators of the symbiotic program. Plant Physiol 136: 3159-3176. (Pubitemid 41096314)
18. Widjaja I, Naumann K, Roth U, Wolf N, Mackey D, et al. (2009) Combining subproteome enrichment and rubisco depletion enables identification of low abundance proteins differentially regulated during plant defense. Proteomics 9: 138-147.
19. Bray EA (2002) Classification of genes differentially expressed during waterdeficit stress in Arabidopsis thaliana : an analysis using microarray and differential expression data. Ann Bot 89: 803-811.
20. Kreps JA, Wu Y, Chang HS, Zhu T, Wang X, et al. (2002) Transcriptome changes for Arabidopsis in response to salt, osmotic, and cold stress. Plant Physiol 130: 2129-2141. (Pubitemid 36035209)
21. Malakshah SN, Rezaei MH, Heidari M, Salekdeh GH (2007) Proteomics reveals new salt responsive proteins associated with rice plasma membrane. Biosci Biotechnol Biochem 71: 2144-2154. (Pubitemid 350113097)
22. Lefebvre B, Timmers T, Mbengue M, Moreau S, Hervé C, et al. (2010) A remorin protein interacts with symbiotic receptors and regulates bacterial infection. Proc Natl Acad Sci USA 107: 2343-2348.
23. Tóth K, Stratil TF, Madsen EB, Ye J, Popp C, et al. (2012) Functional domain analysis of the remorin protein LjSYMREM1 in Lotus japonicas. PloS One 7: e30817.
24. Stockinger EJ, Gilmour SJ, Thomashow MF (1997) Arabidopsis thaliana CBF1 encodes an AP2 domain-containing transcriptional activator that binds to the Crepeat/ DRE, a cis-acting DNA regulatory element that stimulates transcription in response to low temperature and water deficit. Proc Natl Acad Sci USA 94: 1035-1040.
25. Liu Q, Kasuga M, Sakuma Y, Abe H, Miura S, et al. (1998) Two transcription factors, DREB1 and DREB2, with an EREBP/AP2 DNA binding domain separate two cellular signal transduction pathways in Drought- and Low- Temperature-Responsive gene expression, respectively, in Arabidopsis. Plant Cell 10: 1391-1406. (Pubitemid 28542172)
26. Dubouzet JG, Sekuma Y, Ito Y, Kasuga M, Dubouzet EG, et al. (2003) OsDREB genes in rice, Oryza sativa L., encode transcription activators that function in drought-, high-salt- and cold-responsive gene expression. Plant J 33: 751-763. (Pubitemid 36325917)
27. Qin F, Kakimoto M, Sakuma Y, Maruyama K, Osakabe Y, et al. (2007) Regulation and functional analysis of ZmDREB2A in response to drought and heat stresses in Zea mays L. Plant J 50: 54-69. (Pubitemid 46493397)
28. Xue GP (2003) The DNA-binding activity of an AP2 transcriptional activator HvCBF2 involved in regulation of low-temperature responsive genes in barley is modulated by temperature. Plant J 33: 373-383.
29. Gilmour SJ, Sebolt AM, Salazar MP, Everard JD, Thomashow MF (2000). Overexpression of the Arabidopsis CBF3 transcriptional activator mimics multiple biochemical changes associated with cold acclimation. Plant Physiol 124: 1854-1865. (Pubitemid 32053511)
30. Wang Q, Guan Y, Wu Y, Chen H, Chen F, et al. (2008) Overexpression of a rice OsDREB1F gene increases salt, drought, and low temperature tolerance in both Arabidopsis and rice. Plant Molecular Biology 67: 589-602.
31. Kizis D, Pagès M (2002) Maize DRE-binding proteins DBF1 and DBF2 are involved in rab17 regulation through the drought-responsive element in an ABA-dependent pathway. Plant J 30: 679-689. (Pubitemid 34696060)
32. Barton L, Newsome SD, Chen FH, Wang H, Guilderson TP, et al. (2009) Agricultural origins and the isotopic identity of domestication in northern China. Proc Natl Acad Sci USA 106, 5523-5528.
33. Lin F, Xu SL, Ni WM, Chu ZQ, Xu ZH, et al. (2003) Identification of ABA-responsive genes in rice shoots via cDNA macroarray. Cell Res 13: 59-68. (Pubitemid 43231862)
34. 2+-responsive cis elements in Arabidopsis. Plant Cell 18: 2733-2748.
35. Chen L, Tu Z, Hussain J, Cong L, Yan Y, et al. (2010) Isolation and heterologous transformation analysis of a pollen-specific promoter from wheat (Triticum aestivum L.). Mol Biol Rep 37: 737-744.
36. Bechtold N, Pelletier G (1998) In planta Agrobacterium Mediated transformation of adult Arabidopsis thaliana plants by vacuum infiltration. Methods in Molecular Biology 82: 259-266.
37. Zhao LN, Liu FX, Xu WY, Di C, Zhou SX, et al. (2009) Increased expression of OsSPX1 enhances cold/subfreezing tolerance in tobacco and Arabidopsis thaliana. Plant Biotechnol J 7: 550-561.
38. Bettinger RL, Barton L, Morgan C (2010) The origins of food production in north China: A different kind of agricultural revolution. Evolutionary Anthropology 19: 9-21.
39. Burkhard P, Stetefeld J, Strelkov SV (2001) Coiled coils: a highly versatile protein folding motif. Trends Cell Biol 11: 82-88. (Pubitemid 32144755)
40. Chen L, Song Y, Li S, Zhang L, Zou C, et al. (2012) The role of WRKY transcription factors in plant abiotic stresses. BBA-Gene Regul 1819: 120-128.
41. Busk PK, Pagès M (1998) Regulation of abscisic acid-induced transcription. Plant Mol Biol 37: 425-435.
42. Rock C (2000) Pathways to abscisic acid-regulated gene expression. New Phytol 148: 357-396.
43. Yamaguchi-Shinozaki K, Shinozaki K (2006) Transcriptional regulatory networks in cellular responses and tolerance to dehydration and cold stresses. Ann Rev Plant Biol 57: 781-803. (Pubitemid 44061045)
44. Farmer EE, Moloshok TD, Saxton MJ, Ryan CA (1991) Oligosaccharide signaling in plants. Specificity of oligouronide-enhanced plasma membrane protein phosphorylation. J Biol Chem 266: 3140-3145. (Pubitemid 21909185)
45. Reymond P, Kunz B, Paul-Pletzer K, Grimm R, Eckerskorn C, et al. (1996) Cloning of a cDNA encoding a plasma membrane-associated, uronide binding phosphoprotein with physical properties similar to viral movement proteins. Plant Cell 8: 2265-2276. (Pubitemid 126446963)
46. Widjaja I, Naumann K, Roth U, Wolf N, Mackey D, et al. (2009) Combining subproteome enrichment and Rubisco depletion enables identification of low abundance proteins differentially regulated during plant defense. Proteomics 9: 138-147.