DOI QR코드

DOI QR Code

A novel WD40 protein, BnSWD1, is involved in salt stress in Brassica napus

  • Lee, Sang-Hun (Plant Systems Engineering Research Center, Korea Research Institute of Bioscience and Biotechnology) ;
  • Lee, Jun-Hee (Plant Systems Engineering Research Center, Korea Research Institute of Bioscience and Biotechnology) ;
  • Paek, Kyung-Hee (School of Life Sciences and Biotechnology, Korea University) ;
  • Kwon, Suk-Yoon (Plant Systems Engineering Research Center, Korea Research Institute of Bioscience and Biotechnology) ;
  • Cho, Hye-Sun (Plant Systems Engineering Research Center, Korea Research Institute of Bioscience and Biotechnology) ;
  • Kim, Shin-Je (FnP Co., Ltd.) ;
  • Park, Jeong-Mee (Plant Systems Engineering Research Center, Korea Research Institute of Bioscience and Biotechnology)
  • Received : 2010.01.06
  • Accepted : 2010.02.19
  • Published : 2010.06.30

Abstract

Genes that are expressed early in specific response to high salinity conditions were isolated from rapeseed plant (Brassica napus L.) using an mRNA differential display method. Five PCR fragments (DD1.5) were isolated that were induced by, but showed different response kinetics to, 200 mM NaCl. Nucleotide sequence analysis and homology search revealed that the deduced amino sequences of three of the five cDNA fragments showed considerable similarity to those of ${\beta}$-mannosidase (DD1), tomato Pti-6 proteins (DD5), and the tobacco harpin-induced protein hin1 (DD4), respectively. In contrast, the remaining clones, DD3 and DD2, did not correspond to any substantial existing annotation. Using the DD3 fragment as a probe, we isolated a full-length cDNA clone from the cDNA library, which we termed BnSWD1 (Brassica napus salt responsive WD40 1). The predicted amino-acid sequence of BnSWD1 contains eight WD40 repeats and is conserved in all eukaryotes. Notably, the BnSWD1 gene is expressed at high levels under salt-stress conditions. Furthermore, we found that BnSWD1 was upregulated after treatment with abscisic acid, salicylic acid, and methyl jasmonate. Our study suggests that BnSWD1, which is a novel WD40 repeat-containing protein, has a function in salt-stress responses in plants, possibly via abscisic acid-dependent and/or -independent signaling pathways.

Keywords

References

  1. Ach RA, Taranto P, Gruissem W (1997) A conserved family of WD-40 proteins binds to the retinoblastoma protein in both plants and animals. Plant Cell 9:1595-1606
  2. Ausubel FM, Brent R, Kingston RE, Moore DD, Seidman JG, Smith JA, Struhl K (1989) Current protocol in molecular biology. Greene/Wiley, New York
  3. Bonnet J, Romier C, Tora L, Devys D (2008) Zinc-finger UBPs: regulators of deubiquitylation. Trends Biochem Sci 33:369-375 https://doi.org/10.1016/j.tibs.2008.05.005
  4. Church GM, Gilbert W (1984) Genomic sequencing. Proc Natl Acad Sci USA 81:1991-1995 https://doi.org/10.1073/pnas.81.7.1991
  5. Cohn MA, Kowal P, Yang K, Haas W, Huang TT, Gygi SP, D'Andrea AD (2007) A UAF1-containing multisubunit protein complex regulates the Fanconi anemia pathway. Mol Cell 28:786-797 https://doi.org/10.1016/j.molcel.2007.09.031
  6. Cohn MA, Kee Y, Haas W, Gygi SP, D'Andrea AD (2009) UAF1 is a subunit of multiple deubiquitinating enzyme complexes. J Biol Chem 284:5343-5351
  7. Cote-Martin A, Moody C, Fradet-Turcotte A, D'Abramo CM, Lehoux M, Joubert S, Poirier GG, Coulombe B, Laimins LA, Archambault J (2008) Human papillomavirus E1 helicase interacts with the WD repeat protein p80 to promote maintenance of the viral genome in keratinocytes. J Virol 82:1271-1283 https://doi.org/10.1128/JVI.01405-07
  8. Downing WL, Mauxion F, Fauvarque MO, Reviron MP, de Vienne D, Vartanian N, Giraudat J (1992) A Brassica napus transcript encoding a protein related to the Ku¨nitz protease inhibitor family accumulates upon water stress in leaves, not in seeds. Plant J 2:685-693
  9. Forsthoefel NR, Cushman MAF, Cushman JC (1995) Posttranscriptional and posttranslational control of enolase expression in the facultative crassulacean acid metabolism plant Mesembryanthemum crystallinum L. Plant Physiol 108:1185-1195 https://doi.org/10.1104/pp.108.3.1185
  10. Garcia AB, Engler J, Iyer S, Gerats T, Van Montagu M, Caplan AB (1997) Effects of Osmoprotectants upon NaCl Stress in Rice. Plant Physiol 115:159-169
  11. Goormachtig S, Valerio-Lepiniex M, Szczyglowski K, Van Montagu M, Holsters M, de Bruijn FJ (1995) Use of differential display to identify novel Sesbania rostrata genes enhanced by Azorhizobium caulinodans infection. Mol Plant Microbe Interact 8:816-824 https://doi.org/10.1094/MPMI-8-0816
  12. Gopalan S, Wei W, He SY (1996) hrp gene-dependent induction of hin1: a plant gene activated rapidly by both harpins and the avrPto gene-mediated signal. Plant J 10:591-600 https://doi.org/10.1046/j.1365-313X.1996.10040591.x
  13. Ingram J, Bartels D (1996) The molecular basis of dehydration tolerance in plants. Annu Rev Plant Phsiol Plant Mol Biol 47:377-403 https://doi.org/10.1146/annurev.arplant.47.1.377
  14. Ishitani M, Nakamura T, Han SY, Takabe T (1995) Expression of the betaine aldehyde dehydrogenase gene in barley in response to osmotic stress and abscisic acid. Plant Mol Biol 27:307-315 https://doi.org/10.1007/BF00020185
  15. Liang P, Pardee AB (1992) Differential display of eukaryotic messenger RNA by means of the polymerase chain reaction. Science 257:967-971 https://doi.org/10.1126/science.1354393
  16. Liu Q, Kasuga M, Sakuma Y, Abe H, Miura S, Yamaguchi-Shinozaki K, Shinozaki K (1998) Two transcription factor, DREB1 and DREB2, with an EREBP/AP2 DNA binding domain separate two cellular signal transduction pathways in drought- and lowtemperature- responsive gene expression, respectively, in Arabidopsis. Plant Cell 10:1391-1406
  17. Love KR, Catic A, Schlieker C, Ploegh HL (2007) Mechanisms, biology and inhibitors of deubiquitinating enzymes. Nat Chem Biol 3:697-705 https://doi.org/10.1038/nchembio.2007.43
  18. Ma H (1994) GTP-binding proteins in plants: new members of an old family. Plant Mol Biol 26:1611-1636 https://doi.org/10.1007/BF00016493
  19. Mauch-Mani B, Mauch F (2005) The role of abscisic acid in plant- pathogen interactions. Curr Opin Plant Biol 8:409-414 https://doi.org/10.1016/j.pbi.2005.05.015
  20. McNellis TW, von Arnim AG, Araki T, Komeda Y, Misera S, Deng X-W (1994) Genetic and molecular analysis of an allelic series of cop1 mutants suggests functional roles for the multiple protein domains. Plant Cell 6:487-500
  21. Molina A, Olmedo FG (1997) Enhanced tolerance to bacterial pathogens caused by the transgenic expression of barley lipid transfer protein LTP2. Plant J 12:669-675 https://doi.org/10.1046/j.1365-313X.1997.00669.x
  22. Molina A, Diaz I, Vasil IK, Carbonero P (1996) Two cold-inducible genes encoding lipid transfer protein LTP4 from barley show differential responses to bacterial pathogens. Mol Gen Genet 252:162-168 https://doi.org/10.1007/BF02173216
  23. Naot D, Hayyim GB, Eshdat Y, Holland D (1995) Drought, heat and salt stress induce the expression of a citrus homologue of an atypical late-embryogenesis Lea5 gene. Plant Mol Biol 27:619-622 https://doi.org/10.1007/BF00019327
  24. Neer EJ, Schmidt CJ, Nambudripad R, Smith TF (1994) The ancient regulatory-protein family of WD-repeat proteins. Nature 371:297-300 https://doi.org/10.1038/371297a0
  25. Park JM, Park CJ, Lee SB, Ham BK, Shin R, Paek KH (2001) Overexpression of the tobacco Tsi1 gene encoding an EREBP/AP2-type transcription factor enhances resistance against pathogen attack and osmotic stress in tobacco. Plant Cell 13:1035-1046
  26. Park J, Lee BS, Choi JK, Means RE, Choe J, Jung JU (2002) Herpesviral protein targets a cellular WD repeat endosomal protein to down regulate T lymphocyte receptor expression. Immunity 17:221-233 https://doi.org/10.1016/S1074-7613(02)00368-0
  27. Park J, Cho NH, Choi JK, Feng P, Choe J, Jung JU (2003) Distinct roles of cellular Lck and p80 proteins in herpesvirus saimiri Tip function on lipid rafts. J Virol 77:9041-9051 https://doi.org/10.1128/JVI.77.16.9041-9051.2003
  28. Potlakayala SD, Reed DW, Covello PS, Fobert PR (2007) Systemic acquired resistance in canola is linked with pathogenesis-related gene expression and requires salicylic Acid. Phytopathol 97:794-802 https://doi.org/10.1094/PHYTO-97-7-0794
  29. Reviron MP, Vartanian N, Sallantin M, Huet JC, Pernollet JC, de Vienne D (1992) Characterization of a novel protein induced by progressive or rapid drought and salinity in Brassica napus leaves. Plant Physiol 100:1486-1493 https://doi.org/10.1104/pp.100.3.1486
  30. Reymond P, Farmer EE (1998) Jasmonate and salicylate as global signals for defense gene expression. Curr Opin Plant Biol 1:404-411 https://doi.org/10.1016/S1369-5266(98)80264-1
  31. Shinozaki K, Yamaguchi-Shinozaki K (1997) Gene expression and signal transduction in water-stress response. Plant Physiol 115:327-334 https://doi.org/10.1104/pp.115.2.327
  32. Smith TF, Gaitatzes C, Saxena K, Neer EJ (1999) The WD repeat: a common architecture for diverse functions. Trends Biochem Sci 24:181-185 https://doi.org/10.1016/S0968-0004(99)01384-5
  33. Stockinger EJ, Gilmour SJ, Thomashow MF (1997) Arabidopsis thaliana CBF1 encodes an AP2 domain-containing transcriptional activator that binds to the C-repeat/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 https://doi.org/10.1073/pnas.94.3.1035
  34. Toroser D, Huber SC (1997) Protein phosphorylation as a mechanism for osmotic-stress activation of sucrose-phosphate synthase in spinach leaves. Plant Physiol 114:947-955 https://doi.org/10.1104/pp.114.3.947
  35. Urao T, Shinozaki KY, Urao S, Shinozaki K (1993) An Arabidopsis myb homolog is induced by dehydaration stress and its gene product binds to the conserved MYB recognition sequence. Plant Cell 5:1529-1539
  36. van der Voorn L, Ploegh HL (1992) The WD-40 repeat. FEBS Lett 307:131-134 https://doi.org/10.1016/0014-5793(92)80751-2
  37. Verbruggen N, Villarroel R, Montagu MV (1993) Osmoregulation of a pyroline-5-carboxlate reductase gene in Arabidopsis thaliana. Plant Physiol 103:771-781 https://doi.org/10.1104/pp.103.3.771
  38. Walker AR, Davison PA, Bolognesi-Winfield AC, James CM, Srinivasan N, Blundell TL, Esch JJ, Marks MD, Gray JC (1999) The TRANSPARENT TESTA GLABRA1 locus, which regulates trichome differentiation and anthocyanin biosynthesis in Arabidopsis, encodes a WD40 repeat protein. Plant Cell 11:1337-1350
  39. Xiong L, Zhu JK (2001) Abiotic stress signal transduction in plants: molecular and genetic perspectives. Physiol Plant 112:152-166 https://doi.org/10.1034/j.1399-3054.2001.1120202.x
  40. Xiong L, Zhu JK (2002) Molecular and genetic aspects of plant responses to osmotic stress. Plant Cell Environ 25:131-139 https://doi.org/10.1046/j.1365-3040.2002.00782.x
  41. Xue X, Liu A, Hua X (2009) Proline accumulation and transcriptional regulation of proline biosynthesis and degradation in Brassica napus. BMB Rep 42:28-34 https://doi.org/10.5483/BMBRep.2009.42.1.028
  42. Zhu B, Chen TH, Li PH (1995) Activation of two osmotin-like protein genes by abiotic stimuli and fungal pathogen in transgenic potato plants. Plant Physiol 108:929-937 https://doi.org/10.1104/pp.108.3.929
  43. Zhu JQ, Zhang JT, Tang RJ, Lv QD, Wang QQ, Yang L, Zhang HX (2009) Molecular characterization of ThIPK2, an inositol polyphosphate kinase gene homolog from Thellungiella halophila, and its heterologous expression to improve abiotic stress tolerance in Brassica napus. Physiol Plant 136:407-425 https://doi.org/10.1111/j.1399-3054.2009.01235.x

Cited by

  1. Physio-biochemical analysis and transcript profiling of Saccharum officinarum L. submitted to salt stress vol.33, pp.4, 2010, https://doi.org/10.1007/s11738-010-0676-6
  2. Structure and regulatory networks of WD40 protein in plants vol.21, pp.suppl1, 2010, https://doi.org/10.1007/s13562-012-0134-1
  3. Isolation and characterization of cold inducible genes in carrot by suppression subtractive hybridization vol.57, pp.1, 2010, https://doi.org/10.1007/s10535-012-0250-8
  4. The MrWD40-1 Gene of Chinese Bayberry (Myrica rubra) Interacts with MYB and bHLH to Enhance Anthocyanin Accumulation vol.31, pp.6, 2010, https://doi.org/10.1007/s11105-013-0621-0
  5. Physiological and comparative proteomic analyses of Thai jasmine rice and two check cultivars in response to drought stress vol.9, pp.1, 2010, https://doi.org/10.1080/17429145.2012.752042
  6. Identification of TaWD40D, a wheat WD40 repeat-containing protein that is associated with plant tolerance to abiotic stresses vol.34, pp.3, 2015, https://doi.org/10.1007/s00299-014-1717-1
  7. Mechanisms on Boron-Induced Alleviation of Aluminum-Toxicity in Citrus grandis Seedlings at a Transcriptional Level Revealed by cDNA-AFLP Analysis vol.10, pp.3, 2015, https://doi.org/10.1371/journal.pone.0115485
  8. Fagopyrum tataricum FtWD40 Functions as a Positive Regulator of Anthocyanin Biosynthesis in Transgenic Tobacco vol.36, pp.3, 2017, https://doi.org/10.1007/s00344-017-9678-6
  9. Identification of Genes Involved in the Responses of Tangor (C. reticulata × C. sinensis) to Drought Stress vol.2017, pp.None, 2010, https://doi.org/10.1155/2017/8068725
  10. A miniature inverted-repeat transposable element, AddIn-MITE, located inside a WD40 gene is conserved in Andropogoneae grasses vol.7, pp.None, 2010, https://doi.org/10.7717/peerj.6080
  11. Transcriptome profiling of raspberry ( Rubus idaeus Var. Amira) in response to infection by tomato ringspot virus (ToRSV) vol.6, pp.8, 2020, https://doi.org/10.1016/j.heliyon.2020.e04518
  12. Characterization of Transcriptome Expression: The Response of Isatis indigotica to Salt Stress vol.67, pp.6, 2010, https://doi.org/10.1134/s1021443720060163